Reactive oxygen species and cancer: A complex interaction
Elevated levels of Reactive Oxygen Species (ROS), increased antioxidant ability and the maintenance of redox homeostasis can cumulatively contribute to tumor progression and metastasis. The sources and the role of ROS in a heterogeneous tumor microenvironment can vary at different stages of tumor: i...
Saved in:
Published in | Cancer letters Vol. 452; pp. 132 - 143 |
---|---|
Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Ireland
Elsevier B.V
28.06.2019
Elsevier Limited |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Elevated levels of Reactive Oxygen Species (ROS), increased antioxidant ability and the maintenance of redox homeostasis can cumulatively contribute to tumor progression and metastasis. The sources and the role of ROS in a heterogeneous tumor microenvironment can vary at different stages of tumor: initiation, development, and progression, thus making it a complex subject. In this review, we have summarized the sources of ROS generation in cancer cells, its role in the tumor microenvironment, the possible functions of ROS and its important scavenger systems in tumor progression with special emphasis on solid tumors.
•ROS is generated from Mitochondrial and Extra-mitochondrial sources and NOX4 appears to play a significant role in ROS generation in Solid tumors.•Tumor cells upregulate antioxidant defense and Redox balance influences tumor progression.•ROS is an integral component of Tumor microenvironment due to Hypoxia Re-oxygenation- and influences immunity.•ROS mediated cell signaling pathways offer attractive targets for therapeutic intervention. |
---|---|
AbstractList | Elevated levels of Reactive Oxygen Species (ROS), increased antioxidant ability and the maintenance of redox homeostasis can cumulatively contribute to tumor progression and metastasis. The sources and the role of ROS in a heterogeneous tumor microenvironment can vary at different stages of tumor: initiation, development, and progression, thus making it a complex subject. In this review, we have summarized the sources of ROS generation in cancer cells, its role in the tumor microenvironment, the possible functions of ROS and its important scavenger systems in tumor progression with special emphasis on solid tumors. Elevated levels of Reactive Oxygen Species (ROS), increased antioxidant ability and the maintenance of redox homeostasis can cumulatively contribute to tumor progression and metastasis. The sources and the role of ROS in a heterogeneous tumor microenvironment can vary at different stages of tumor: initiation, development, and progression, thus making it a complex subject. In this review, we have summarized the sources of ROS generation in cancer cells, its role in the tumor microenvironment, the possible functions of ROS and its important scavenger systems in tumor progression with special emphasis on solid tumors. •ROS is generated from Mitochondrial and Extra-mitochondrial sources and NOX4 appears to play a significant role in ROS generation in Solid tumors.•Tumor cells upregulate antioxidant defense and Redox balance influences tumor progression.•ROS is an integral component of Tumor microenvironment due to Hypoxia Re-oxygenation- and influences immunity.•ROS mediated cell signaling pathways offer attractive targets for therapeutic intervention. Elevated levels of Reactive Oxygen Species (ROS), increased antioxidant ability and the maintenance of redox homeostasis can cumulatively contribute to tumor progression and metastasis. The sources and the role of ROS in a heterogeneous tumor microenvironment can vary at different stages of tumor: initiation, development, and progression, thus making it a complex subject. In this review, we have summarized the sources of ROS generation in cancer cells, its role in the tumor microenvironment, the possible functions of ROS and its important scavenger systems in tumor progression with special emphasis on solid tumors.Elevated levels of Reactive Oxygen Species (ROS), increased antioxidant ability and the maintenance of redox homeostasis can cumulatively contribute to tumor progression and metastasis. The sources and the role of ROS in a heterogeneous tumor microenvironment can vary at different stages of tumor: initiation, development, and progression, thus making it a complex subject. In this review, we have summarized the sources of ROS generation in cancer cells, its role in the tumor microenvironment, the possible functions of ROS and its important scavenger systems in tumor progression with special emphasis on solid tumors. |
Author | Saikolappan, Sankaralingam Koul, Sweaty Shishodia, Gauri Koul, Hari K. Kumar, Binod |
Author_xml | – sequence: 1 givenname: Sankaralingam surname: Saikolappan fullname: Saikolappan, Sankaralingam organization: Department of Biochemistry and Molecular Biology, USA – sequence: 2 givenname: Binod surname: Kumar fullname: Kumar, Binod organization: The James Buchanan Brady Urologic Institute and Department of Urology, Johns Hopkins School of Medicine, Baltimore, MD, USA – sequence: 3 givenname: Gauri surname: Shishodia fullname: Shishodia, Gauri organization: Department of Biochemistry and Molecular Biology, USA – sequence: 4 givenname: Sweaty surname: Koul fullname: Koul, Sweaty organization: Department of Urology, LSU Health Sciences Center, 1501 Kings Highway, Shreveport, LA, 71130, USA – sequence: 5 givenname: Hari K. orcidid: 0000-0002-3747-4678 surname: Koul fullname: Koul, Hari K. email: hkoul@lsuhsc.edu organization: Department of Biochemistry and Molecular Biology, USA |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/30905813$$D View this record in MEDLINE/PubMed |
BookMark | eNqFkU1rGzEQhkVJaZy0_6CUhV562e3oa6UNpRBCvyAQCM1ZKNJskbuWXGkd4n9fOU4uvviky_O8M5r3jJzEFJGQ9xQ6CrT_vOycjRPOHQM6dMA7YPCKLKhWrFWDhhOyAA6i5ZrLU3JWyhIApFDyDTnlMIDUlC_IcIvWzeEBm_S4_YOxKWt0AUtjo2_qAIf5orlsXFqtJ3xsQpwx74QU35LXo50Kvnt-z8nd92-_r3621zc_fl1dXrdOCD63tGe016PSAzLgvfajHhR44SVo30vnR-zvhZaaO8HZIJQGz6kHrzgfRy35Ofm0z13n9G-DZTarUBxOk42YNsUwOijOqqoq-vEAXaZNjnU7w56GSy37Sn14pjb3K_RmncPK5q15OUoFLvaAy6mUjKNxYba7P8_ZhslQMLsGzNLsGzC7BgxwUxuosjiQX_KPaF_3GtZTPgTMptQa6vl9yOhm41M4FvDlIMBNIQZnp7-4Pa7_B-72sss |
CitedBy_id | crossref_primary_10_1016_j_prp_2023_154664 crossref_primary_10_3390_antiox13040475 crossref_primary_10_1084_jem_20240445 crossref_primary_10_3390_jcm11010126 crossref_primary_10_3390_pharmaceutics16020175 crossref_primary_10_1002_smtd_202400945 crossref_primary_10_1021_acs_analchem_2c00400 crossref_primary_10_1084_jem_20191226 crossref_primary_10_1186_s40659_024_00577_z crossref_primary_10_3390_molecules25204864 crossref_primary_10_1038_s43246_024_00623_z crossref_primary_10_3390_bios12070478 crossref_primary_10_3390_stresses3020036 crossref_primary_10_1039_D0CC02245D crossref_primary_10_1111_apha_13351 crossref_primary_10_1016_j_jconrel_2024_09_008 crossref_primary_10_1016_j_cej_2024_150291 crossref_primary_10_1089_ars_2022_0096 crossref_primary_10_1002_adhm_202301853 crossref_primary_10_1021_acs_analchem_2c02036 crossref_primary_10_1007_s00775_021_01862_y crossref_primary_10_15252_embr_202153140 crossref_primary_10_3390_chemosensors13030104 crossref_primary_10_1016_j_snb_2022_133146 crossref_primary_10_3390_antiox12020367 crossref_primary_10_4103_jioh_jioh_215_22 crossref_primary_10_1155_2022_6177477 crossref_primary_10_5812_ijpr_138856 crossref_primary_10_1186_s12863_022_01032_2 crossref_primary_10_1515_med_2024_0999 crossref_primary_10_1016_j_sajb_2024_06_033 crossref_primary_10_1016_j_saa_2023_123430 crossref_primary_10_1021_acs_inorgchem_4c00232 crossref_primary_10_1080_13102818_2022_2082318 crossref_primary_10_1242_jeb_196352 crossref_primary_10_1016_j_lfs_2019_117145 crossref_primary_10_1186_s12951_025_03264_7 crossref_primary_10_1093_jaoacint_qsae054 crossref_primary_10_1016_j_bbcan_2024_189154 crossref_primary_10_1021_acs_chemmater_1c03346 crossref_primary_10_1039_D2BM00421F crossref_primary_10_1007_s10555_021_10009_z crossref_primary_10_3390_cancers12051236 crossref_primary_10_1039_D2NJ05987H crossref_primary_10_1016_j_colsurfb_2022_113117 crossref_primary_10_1016_j_colsurfb_2024_114326 crossref_primary_10_1016_j_ccell_2019_12_012 crossref_primary_10_1002_jbt_22900 crossref_primary_10_1142_S1793292024300081 crossref_primary_10_1002_med_21734 crossref_primary_10_3390_mi12091122 crossref_primary_10_1021_acsanm_4c06311 crossref_primary_10_1007_s13577_024_01068_9 crossref_primary_10_3390_antiox10060949 crossref_primary_10_1167_iovs_65_2_30 crossref_primary_10_3892_ol_2023_14200 crossref_primary_10_1021_acs_nanolett_3c03928 crossref_primary_10_1039_D5CC00055F crossref_primary_10_3390_cancers14051259 crossref_primary_10_1149_1945_7111_acd41f crossref_primary_10_3390_antiox10020169 crossref_primary_10_3389_fphar_2020_610205 crossref_primary_10_3390_cells13191666 crossref_primary_10_3390_molecules27217537 crossref_primary_10_3390_cells13171428 crossref_primary_10_1016_j_colsurfb_2023_113220 crossref_primary_10_1039_D3OB00782K crossref_primary_10_1016_j_snb_2023_134615 crossref_primary_10_3390_ijms241210283 crossref_primary_10_1515_hmbci_2023_0012 crossref_primary_10_2174_0113816128296710240404040232 crossref_primary_10_1016_j_jinorgbio_2023_112365 crossref_primary_10_1016_j_snb_2022_132260 crossref_primary_10_3390_ijms232214162 crossref_primary_10_1002_admt_202201929 crossref_primary_10_1016_j_ijbiomac_2024_139094 crossref_primary_10_1039_D3RA04074G crossref_primary_10_1016_j_mrrev_2021_108365 crossref_primary_10_1016_j_colsurfa_2023_133101 crossref_primary_10_2174_0929866527666200413101017 crossref_primary_10_1007_s12672_021_00439_0 crossref_primary_10_1039_D2AN00690A crossref_primary_10_1158_1940_6207_CAPR_23_0162 crossref_primary_10_1002_smll_202106342 crossref_primary_10_3390_antiox11010072 crossref_primary_10_1039_D1TB00058F crossref_primary_10_1039_D4SC04261A crossref_primary_10_1016_j_bioorg_2024_107730 crossref_primary_10_1021_acs_chemrestox_2c00396 crossref_primary_10_1155_2020_2415324 crossref_primary_10_1016_j_impact_2024_100521 crossref_primary_10_1248_cpb_c24_00056 crossref_primary_10_3390_ijms25179255 crossref_primary_10_1002_bkcs_12811 crossref_primary_10_1021_jacs_2c12892 crossref_primary_10_1038_s41388_020_1191_x crossref_primary_10_3389_fonc_2022_982751 crossref_primary_10_1002_jgm_3581 crossref_primary_10_1016_j_apsb_2024_10_015 crossref_primary_10_1016_j_lfs_2020_117403 crossref_primary_10_1016_j_molstruc_2024_141212 crossref_primary_10_1007_s11356_021_15922_y crossref_primary_10_1016_j_bioactmat_2021_08_012 crossref_primary_10_1016_j_phrs_2021_105709 crossref_primary_10_3390_biom9110735 crossref_primary_10_3390_molecules28176417 crossref_primary_10_3390_ijms23052657 crossref_primary_10_3390_ijms232012169 crossref_primary_10_1016_j_biomaterials_2019_119500 crossref_primary_10_1016_j_heliyon_2023_e19896 crossref_primary_10_1016_j_molstruc_2024_138729 crossref_primary_10_1039_D2TB00789D crossref_primary_10_1016_j_biopha_2024_117063 crossref_primary_10_1016_j_phrs_2022_106241 crossref_primary_10_1039_D1TB01036K crossref_primary_10_1039_D3DT00317E crossref_primary_10_3390_cancers14071806 crossref_primary_10_1016_j_micromeso_2021_110905 crossref_primary_10_1016_j_jcis_2022_08_060 crossref_primary_10_1039_D4TB01934B crossref_primary_10_1016_j_bbrc_2023_149167 crossref_primary_10_3389_fimmu_2023_1130172 crossref_primary_10_1016_j_ejphar_2023_175586 crossref_primary_10_3389_fphar_2021_758320 crossref_primary_10_3390_jmp5010007 crossref_primary_10_1016_j_lfs_2020_117534 crossref_primary_10_3390_ijms22158335 crossref_primary_10_1002_adhm_202405124 crossref_primary_10_3390_ijms23010080 crossref_primary_10_1007_s12032_022_01900_y crossref_primary_10_1016_j_cej_2021_132303 crossref_primary_10_1073_pnas_2020152118 crossref_primary_10_1186_s40364_022_00446_5 crossref_primary_10_3390_molecules27010293 crossref_primary_10_1186_s12951_022_01591_7 crossref_primary_10_1021_acsnano_2c05379 crossref_primary_10_3390_cancers13205037 crossref_primary_10_1253_circj_CJ_22_0628 crossref_primary_10_1021_acs_nanolett_4c02178 crossref_primary_10_1016_j_bbcan_2023_188867 crossref_primary_10_1016_j_biopha_2021_111928 crossref_primary_10_32708_uutfd_1124693 crossref_primary_10_1021_jacs_1c11856 crossref_primary_10_2174_0118715206317999240708062744 crossref_primary_10_3390_pr9091549 crossref_primary_10_1016_j_ccr_2023_215563 crossref_primary_10_1038_s41419_021_03771_z crossref_primary_10_1002_ddr_22084 crossref_primary_10_1016_j_sajb_2023_05_042 crossref_primary_10_1080_09603123_2021_2023113 crossref_primary_10_1149_1945_7111_ab8367 crossref_primary_10_1186_s12935_021_02150_0 crossref_primary_10_1039_D1NJ03690D crossref_primary_10_3389_fonc_2020_00942 crossref_primary_10_3390_molecules28135202 crossref_primary_10_1016_j_aquatox_2020_105622 crossref_primary_10_1016_j_phymed_2024_155945 crossref_primary_10_1016_j_scitotenv_2024_172567 crossref_primary_10_1016_j_talanta_2024_126515 crossref_primary_10_3892_mmr_2022_12819 crossref_primary_10_1002_tox_23752 crossref_primary_10_1039_c9mt00133f crossref_primary_10_2174_0115680266305736240725052825 crossref_primary_10_1016_j_bbalip_2019_158596 crossref_primary_10_1021_acsami_4c16518 crossref_primary_10_1002_mco2_519 crossref_primary_10_1002_ptr_8157 crossref_primary_10_1016_j_focha_2024_100871 crossref_primary_10_1021_acs_jmedchem_4c00023 crossref_primary_10_1039_D4NJ04125A crossref_primary_10_1016_j_sajb_2024_07_044 crossref_primary_10_3390_chemistry5010017 crossref_primary_10_1016_j_tetlet_2021_153176 crossref_primary_10_1002_kjm2_12684 crossref_primary_10_3389_fmolb_2020_576420 crossref_primary_10_3390_ijms23052702 crossref_primary_10_1002_jcp_29219 crossref_primary_10_1177_1533033820963599 |
Cites_doi | 10.1016/j.currproblcancer.2008.08.002 10.1038/nm.4053 10.1002/mc.22202 10.1016/j.ccr.2006.12.013 10.18632/oncotarget.20497 10.1073/pnas.0408894102 10.1016/j.cell.2015.05.001 10.1038/s41467-017-01269-x 10.1016/j.freeradbiomed.2014.10.773 10.1038/cddis.2016.105 10.1002/pros.22776 10.1091/mbc.e09-12-1003 10.1016/j.freeradbiomed.2007.01.015 10.1016/j.bbamcr.2013.09.018 10.1152/ajpcell.00525.2002 10.1073/pnas.1402012111 10.1371/journal.pone.0013565 10.1126/scisignal.2003638 10.1371/journal.pone.0054206 10.1038/ki.2015.21 10.1158/0008-5472.CAN-16-2204 10.1593/neo.09744 10.1038/srep23135 10.1016/j.gendis.2016.04.002 10.4161/auto.6.8.13547 10.1016/j.fob.2012.05.001 10.1038/onc.2015.498 10.1038/onc.2008.79 10.1016/j.freeradbiomed.2011.07.011 10.1073/pnas.022630199 10.1038/nature07733 10.1002/ijc.29519 10.1093/carcin/21.3.379 10.1073/pnas.1003428107 10.18632/oncotarget.4479 10.1016/j.freeradbiomed.2012.06.016 10.1016/j.cell.2005.02.003 10.1038/onc.2016.225 10.1016/B978-0-12-394384-2.00004-8 10.1186/1476-4598-2-23 10.1038/onc.2011.37 10.1038/nrc3803 10.1016/j.clon.2007.03.001 10.1038/sj.onc.1209600 10.1023/A:1026506011458 10.1038/s41588-018-0078-z 10.1053/j.seminoncol.2015.02.009 10.18632/oncotarget.9821 10.1093/jnci/djx121 10.1038/ncomms14437 10.1038/bjc.2016.440 10.1038/onc.2008.335 10.1016/j.cell.2015.10.025 10.1023/A:1009616228304 10.1158/0008-5472.CAN-08-3359 10.1038/nature03688 10.18632/oncotarget.2197 10.1016/j.freeradbiomed.2016.04.198 10.1016/j.abb.2005.02.021 10.1002/mc.22255 10.1111/apha.12625 10.1016/j.bbrc.2011.05.074 10.7150/ijbs.7224 10.1158/0008-5472.CAN-14-0626 10.1093/carcin/bgg102 10.3389/fimmu.2015.00482 10.1016/j.cell.2016.06.056 10.1016/j.ccr.2008.11.006 10.1002/biof.1200 10.1056/NEJMcibr1405701 10.1016/j.yexcr.2017.02.014 10.1371/journal.pone.0177549 10.1186/2041-9414-4-5 10.1093/jnci/djm135 10.1038/cddis.2013.50 10.18632/oncotarget.2514 10.1016/j.canlet.2008.12.011 10.1016/j.amepre.2013.10.029 10.1038/onc.2008.476 10.1080/2162402X.2015.1062967 10.1038/s41467-018-05676-6 10.1038/bjc.2016.88 10.1016/j.ejphar.2003.10.032 10.1038/nature15726 10.1385/MO:22:1:011 10.1111/imm.12380 10.1096/fj.201601178R 10.1093/carcin/bgn032 10.18632/oncotarget.2025 10.1016/j.bbrc.2010.11.044 10.3857/roj.2016.02012 10.1186/2049-3002-2-17 10.1016/j.ccr.2013.01.022 10.1016/j.ccr.2008.11.003 10.1016/j.semcancer.2017.04.005 10.1097/MPA.0000000000000270 10.1038/s41598-018-21838-4 10.1152/physrev.00044.2005 10.1038/nrc2344 10.3748/wjg.v16.i39.4932 10.1016/S0531-5565(01)00153-X 10.18632/oncotarget.18724 10.1155/2016/3907147 10.1210/me.2010-0340 10.1016/j.ccell.2015.01.007 10.1038/bjc.2013.396 10.1016/S0002-9440(10)63606-1 10.1136/jcp.2005.027664 10.1074/jbc.275.10.7087 10.1016/j.ccr.2012.05.016 10.1038/nature10189 10.1038/s41388-017-0109-8 10.1155/2016/2428153 10.1038/onc.2016.454 10.1038/nm.4045 10.1165/ajrcmb.12.1.7529030 10.1615/CritRevOncog.v20.i5-6.130 10.1038/ng.2279 10.1158/0008-5472.CAN-07-5259 10.1016/j.ccr.2010.05.026 10.1186/1471-2407-14-252 10.1042/bse0470053 10.1245/s10434-011-2040-5 10.1097/CAD.0000000000000198 10.7150/ijbs.20052 10.3892/or.2016.4766 10.1016/j.cell.2013.03.021 10.1007/s40484-014-0032-8 10.1038/srep39692 10.1016/j.redox.2017.05.016 10.1371/journal.pone.0087204 10.1155/2016/6823471 |
ContentType | Journal Article |
Copyright | 2019 Elsevier B.V. Copyright © 2019 Elsevier B.V. All rights reserved. 2019. Elsevier B.V. |
Copyright_xml | – notice: 2019 Elsevier B.V. – notice: Copyright © 2019 Elsevier B.V. All rights reserved. – notice: 2019. Elsevier B.V. |
DBID | AAYXX CITATION CGR CUY CVF ECM EIF NPM 7TO 7U9 H94 K9. NAPCQ 7X8 |
DOI | 10.1016/j.canlet.2019.03.020 |
DatabaseName | CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed Oncogenes and Growth Factors Abstracts Virology and AIDS Abstracts AIDS and Cancer Research Abstracts ProQuest Health & Medical Complete (Alumni) Nursing & Allied Health Premium MEDLINE - Academic |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) AIDS and Cancer Research Abstracts ProQuest Health & Medical Complete (Alumni) Nursing & Allied Health Premium Virology and AIDS Abstracts Oncogenes and Growth Factors Abstracts MEDLINE - Academic |
DatabaseTitleList | AIDS and Cancer Research Abstracts MEDLINE - Academic MEDLINE |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine |
EISSN | 1872-7980 |
EndPage | 143 |
ExternalDocumentID | 30905813 10_1016_j_canlet_2019_03_020 S0304383519301764 |
Genre | Research Support, U.S. Gov't, Non-P.H.S Review Research Support, Non-U.S. Gov't Journal Article Research Support, N.I.H., Extramural |
GroupedDBID | --- --K --M .1- .FO .~1 0R~ 1B1 1P~ 1RT 1~. 1~5 29B 4.4 457 4CK 4G. 5GY 5RE 5VS 6J9 6PF 7-5 71M 8FE 8FH 8P~ 9JM AABNK AAEDT AAEDW AAIKJ AAKOC AALRI AAOAW AAQFI AATTM AAWTL AAXKI AAXUO AAYWO ABBQC ABFNM ABFRF ABGSF ABJNI ABMAC ABMZM ABUDA ACDAQ ACGFO ACGFS ACIEU ACIUM ACPRK ACRLP ACVFH ADBBV ADCNI ADEZE ADFRT ADUVX AEBSH AEFWE AEHWI AEIPS AEKER AENEX AEUPX AEVXI AFPUW AFRAH AFRHN AFTJW AFXIZ AGCQF AGHFR AGUBO AGYEJ AHHHB AHMBA AIEXJ AIIUN AIKHN AITUG AJRQY AJUYK AKBMS AKRWK AKYEP ALMA_UNASSIGNED_HOLDINGS AMRAJ ANKPU ANZVX APXCP AXJTR BKEYQ BKOJK BLXMC BNPGV BPHCQ BVXVI CS3 DU5 EBS EFJIC EFKBS EJD EO8 EO9 EP2 EP3 F5P FDB FIRID FNPLU FYGXN G-Q GBLVA IH2 IHE J1W K-O KOM LK8 M29 M41 MO0 N9A O-L O9- OAUVE OC~ OO- OZT P-8 P-9 P2P PC. PQQKQ PROAC Q38 ROL RPZ SCC SDF SDG SDP SEL SES SPCBC SSH SSU SSZ T5K Z5R ~G- 7RV 7X7 8C1 8FI AACTN AAIAV ABLVK ABYKQ AFCTW AFKRA AFKWA AJOXV AMFUW AZQEC BBNVY BENPR BHPHI DOVZS EFLBG FYUFA GUQSH HCIFZ LCYCR M1P M2M M2O M7P RIG .55 .GJ 3O- 53G AAQXK AAYXX ABWVN ABXDB ACRPL ADMUD ADNMO AFFNX AFJKZ AGQPQ AGRDE AGRNS AI. AIGII ASPBG AVWKF AZFZN CITATION FEDTE FGOYB G-2 HED HMK HMO HVGLF HZ~ R2- SAE SEW UDS VH1 WUQ X7M ZGI CGR CUY CVF ECM EIF NPM 7TO 7U9 H94 K9. NAPCQ 7X8 |
ID | FETCH-LOGICAL-c443t-162168f789e20368df8970d4d508d65cdfe6b48583c43294780d31d0d733ff853 |
IEDL.DBID | .~1 |
ISSN | 0304-3835 1872-7980 |
IngestDate | Fri Jul 11 01:03:03 EDT 2025 Wed Aug 13 09:10:55 EDT 2025 Wed Feb 19 02:31:25 EST 2025 Thu Apr 24 23:11:13 EDT 2025 Tue Jul 01 02:29:39 EDT 2025 Fri Feb 23 02:33:51 EST 2024 Tue Aug 26 16:33:40 EDT 2025 |
IsPeerReviewed | true |
IsScholarly | true |
Keywords | CDKN1A ALS PTEN RTK EGFR PCa ADT DHT CSC Nrf2 GATOR1 mROS GC JAK2 GSH FoxO APE1 VEGF IGF1 MAPK Hypoxia Re-Oxygenation EMT SIRT3 TRX1 AR STAT CXCL12 PDAC TEC ARE NOX ROS TGFβ TFAM ATM ATP CRPC Cancer ERK |
Language | English |
License | Copyright © 2019 Elsevier B.V. All rights reserved. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c443t-162168f789e20368df8970d4d508d65cdfe6b48583c43294780d31d0d733ff853 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Review-3 content type line 23 |
ORCID | 0000-0002-3747-4678 |
PMID | 30905813 |
PQID | 2203685856 |
PQPubID | 2031080 |
PageCount | 12 |
ParticipantIDs | proquest_miscellaneous_2197323297 proquest_journals_2203685856 pubmed_primary_30905813 crossref_citationtrail_10_1016_j_canlet_2019_03_020 crossref_primary_10_1016_j_canlet_2019_03_020 elsevier_sciencedirect_doi_10_1016_j_canlet_2019_03_020 elsevier_clinicalkey_doi_10_1016_j_canlet_2019_03_020 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2019-06-28 |
PublicationDateYYYYMMDD | 2019-06-28 |
PublicationDate_xml | – month: 06 year: 2019 text: 2019-06-28 day: 28 |
PublicationDecade | 2010 |
PublicationPlace | Ireland |
PublicationPlace_xml | – name: Ireland – name: Clare |
PublicationTitle | Cancer letters |
PublicationTitleAlternate | Cancer Lett |
PublicationYear | 2019 |
Publisher | Elsevier B.V Elsevier Limited |
Publisher_xml | – name: Elsevier B.V – name: Elsevier Limited |
References | Kumar, Koul, Khandrika, Meacham, Koul (bib6) 2008; 68 WHO (bib2) 2018 Liu, Yao, Li, Geng, Yan, Che, Xu, Zheng (bib72) 2015; 41 Diebold, Chandel (bib15) 2016; 100 Boudreau, Casterline, Rada, Korzeniowska, Leto (bib114) 2012; 53 Pelicano, Lu, Zhou, Zhang, Chen, Hu, Huang (bib140) 2009; 69 Hanley, Mellone, Ford, Thirdborough, Mellows, Frampton, Smith, Harden, Szyndralewiez, Bullock, Noble, Moutasim, King, Vijayanand, Mirnezami, Underwood, Ottensmeier, Thomas (bib40) 2018; 110 Ryoo, Lee, Kwak (bib63) 2016; 2016 Hoogsteen, Marres, van der Kogel, Kaanders (bib76) 2007; 19 Samaranayake, Troccoli, Huynh, Lyles, Kage, Win, Lakshmanan, Kwon, Ban, Chen, Zarco, Jorda, Burnstein, Rai (bib60) 2017; 8 Tan, Sng, How, Chan, Chen, Tan, Wahli, Tan (bib117) 2018 Kim, Sung, Park, Kho, Koo, Park, Goh, Jeon, Oh, Park, Jung, Kim (bib45) 2017; 116 Paranjape, Soundararajan, Werden, Joseph, Taube, Liu, Rodriguez-Canales, Sphyris, Wistuba, Miura, Dhillon, Mahajan, Mahajan, Chang, Ittmann, Maity, Logothetis, Tang, Mani (bib112) 2016; 35 Dolado, Nebreda (bib145) 2008; 14 Farhan, Wang, Gaur, Little, Xu, Zheng (bib107) 2017; 13 Porporato, Sonveaux (bib23) 2015; 2 Chandel, Tuveson (bib58) 2014; 371 Ren, Liu, Wang, Yu, Yang, Chen, Yu, Wang, Li, Wang, Hou, Fang, Yeh, Yang, Yi (bib111) 2014; 5 Hamanaka, Glasauer, Hoover, Yang, Blatt, Mullen, Getsios, Gottardi, DeBerardinis, Lavker, Chandel (bib21) 2013; 6 Trojan, Schaaf, Steidler, Haak, Thalmann, Knoll, Gretz, Alken, Michel (bib57) 2005; 25 Schlaepfer, Nambiar, Ramteke, Kumar, Dhar, Agarwal, Bergman, Graner, Maroni, Singh, Agarwal, Deep (bib104) 2015; 6 Sumbayev, Yasinska (bib92) 2005; 436 Kim, Haraguchi, Ishii, Ohkuma, Okano, Mimori, Eguchi, Yamamoto, Nagano, Sekimoto, Doki, Mori (bib121) 2012; 19 Sullivan, Chandel (bib14) 2014; 2 Jessie, Sun, Irons, Marshall, Wallace, Petros (bib25) 2001; 37 Schultz, Hagan, Datta, Zhang, Freeman, Sikka, Abdel-Mageed, Mondal (bib71) 2014; 9 Lu, Alcivar, Ma, Foo, Zywea, Mahdi, Huo, Kensler, Gatza, Xia (bib141) 2017; 77 Deep, Kumar, Jain, Dhar, Panigrahi, Hussain, Agarwal, El-Elimat, Sica, Oberlies, Agarwal (bib37) 2016; 6 Dolado, Swat, Ajenjo, De Vita, Cuadrado, Nebreda (bib138) 2007; 11 Cho, Choi, Jeong, Kim, Hwang, Shin, Park, Lee (bib89) 2014; 74 Yu (bib18) 2012; 57 Kim, Kang, Cho (bib125) 2013; 33 Tafani, Sansone, Limana, Arcangeli, De Santis, Polese, Fini, Russo (bib98) 2016; 2016 Barnett, Arnold, Mezencev, Chung, Zayzafoon, Odero-Marah (bib142) 2011; 404 Schumacker (bib11) 2015; 27 Yoon, Woo, Kang, Kim, Kwon, Park, Shin, Gwak, Chwae (bib139) 2010; 6 Bell, Emerling, Ricoult, Guarente (bib16) 2011; 30 Muller (bib4) 2000; 23 Le, Stine, Nguyen, Afzal, Sun, Hamaker, Siegel, Gouw, Kang, Yu, Cochran, Sailor, Song, Dang (bib81) 2014; 111 Jajoo, Mukherjea, Watabe, Ramkumar (bib48) 2009; 11 Piskounova, Agathocleous, Murphy, Hu, Huddlestun, Zhao, Leitch, Johnson, DeBerardinis, Morrison (bib59) 2015; 527 Tas, Hansel, Belce, Ilvan, Argon, Camlica, Topuz (bib85) 2005; 22 Zhang, Cao, Xu (bib79) 2014; 2 Loeb, Loeb (bib9) 2000; 21 Balamurugan (bib87) 2016; 138 Shiota, Yokomizo, Naito (bib7) 2011; 51 Robinson, Van Allen, Wu, Schultz, Lonigro, Mosquera, Montgomery, Taplin, Pritchard, Attard, Beltran, Abida, Bradley, Vinson, Cao, Vats, Kunju, Hussain, Feng, Tomlins, Cooney, Smith, Brennan, Siddiqui, Mehra, Chen, Rathkopf, Morris, Solomon, Durack, Reuter, Gopalan, Gao, Loda, Lis, Bowden, Balk, Gaviola, Sougnez, Gupta, Yu, Mostaghel, Cheng, Mulcahy, True, Plymate, Dvinge, Ferraldeschi, Flohr, Miranda, Zafeiriou, Tunariu, Mateo, Perez-Lopez, Demichelis, Robinson, Schiffman, Nanus, Tagawa, Sigaras, Eng, Elemento, Sboner, Heath, Scher, Pienta, Kantoff, de Bono, Rubin, Nelson, Garraway, Sawyers, Chinnaiyan (bib50) 2015; 161 Taylor, Schultz, Hieronymus, Gopalan, Xiao, Carver, Arora, Kaushik, Cerami, Reva, Antipin, Mitsiades, Landers, Dolgalev, Major, Wilson, Socci, Lash, Heguy, Eastham, Scher, Reuter, Scardino, Sander, Sawyers, Gerald (bib49) 2010; 18 Kalo, Kogan-Sakin, Solomon, Bar-Nathan, Shay, Shetzer, Dekel, Goldfinger, Buganim, Stambolsky, Goldstein, Madar, Rotter (bib68) 2012; 125 van de Schootbrugge, Schults, Bussink, Span, Grénman, Pruijn, Kaanders, Boelens (bib94) 2014; 14 Trédan, Galmarini, Patel, Tannock (bib75) 2007; 99 Nogueira, Park, Chen, Xu, Chen, Tonic, Unterman, Hay (bib144) 2008; 14 Zulueta, Yu, Hertig, Thannickal, Hassoun (bib84) 1995; 12 Khandrika, Lieberman, Koul, Kumar, Maroni, Chandhoke, Meacham, Koul (bib93) 2009; 28 Hai, Zhu, Wang, Organ, Shepherd, Tsao (bib95) 2017; 7 Diehn, Cho, Lobo, Kalisky, Dorie, Kulp, Qian, Lam, Ailles, Wong, Joshua, Kaplan, Wapnir, Dirbas, Somlo, Garberoglio, Paz, Shen, Lau, Quake, Brown, Weissman, Clarke (bib118) 2009; 458 Li, Fu, Zheng, He, Niu, Chen, Yin, Qian, Xu, Wang, Sun, Shu, Rui, Liu, Jiang (bib38) 2013; 1833 Barbieri, Baca, Lawrence, Demichelis, Blattner, Theurillat, White, Stojanov, Van Allen, Stransky, Nickerson, Chae, Boysen, Auclair, Onofrio, Park, Kitabayashi, MacDonald, Sheikh, Vuong, Guiducci, Cibulskis, Sivachenko, Carter, Saksena, Voet, Hussain, Ramos, Winckler, Redman, Ardlie, Tewari, Mosquera, Rupp, Wild, Moch, Morrissey, Nelson, Kantoff, Gabriel, Golub, Meyerson, Lander, Getz, Rubin, Garraway (bib56) 2012; 44 Crosas-Molist, Bertran, Rodriguez-Hernandez, Herraiz, Cantelli, Fabra, Sanz-Moreno, Fabregat (bib115) 2017; 36 Weinberg, Hamanaka, Wheaton, Weinberg, Joseph, Lopez, Kalyanaraman, Mutlu, Budinger, Chandel (bib22) 2010; 107 Campisi (bib128) 2005; 120 Ha, Yu (bib136) 2010; 16 Khandrika, Kumar, Koul, Maroni, Koul (bib8) 2009; 282 Network (bib54) 2015; 163 Kunz, Ibrahim (bib80) 2003; 2 Kurkjian, Kummar, Murgo (bib129) 2008; 32 Oben, Alhakeem, McKenna, Brandon, Mani, Noothi, Jinpeng, Akunuru, Dhar, Singh, Liang, Wang, Abdel-Latif, Stills, St Clair, Geiger, Muthusamy, Tohyama, Gupta, Bondada (bib134) 2017; 8 Chen, Gokden, Greene, Mukunyadzi, Kadlubar (bib28) 2002; 62 Beltran, Prandi, Mosquera, Benelli, Puca, Cyrta, Marotz, Giannopoulou, Chakravarthi, Varambally, Tomlins, Nanus, Tagawa, Van Allen, Elemento, Sboner, Garraway, Rubin, Demichelis (bib53) 2016; 22 Simon, Haj-Yehia, Levi-Schaffer (bib20) 2000; 5 Dey, Moraes (bib19) 2000; 275 Deep, Panigrahi (bib103) 2015; 20 Chio, Jafarnejad, Ponz-Sarvise, Park, Rivera, Palm, Wilson, Sangar, Hao, Öhlund, Wright, Filippini, Lee, Da Silva, Schoepfer, Wilkinson, Buscaglia, DeNicola, Tiriac, Hammell, Crawford, Schmidt, Thompson, Pappin, Sonenberg, Tuveson (bib65) 2016; 166 Chouaib, Noman, Kosmatopoulos, Curran (bib96) 2017; 36 Balamurugan, Sterneck (bib91) 2013; 9 Dakubo, Parr, Costello, Franklin, Thayer (bib24) 2006; 59 Kumar, Gabrilovich (bib101) 2014; 143 Moltzahn, Thalmann (bib124) 2013; 2 Bristow, Hill (bib77) 2008; 8 Whitaker, Patel, Howat, Warren, Kay, Sangan, Marioni, Mitchell, Aldridge, Luxton, Massie, Lynch, Neal (bib110) 2013; 109 Chen, Gokden, Greene, Green, Kadlubar (bib27) 2003; 24 Millar, Phan, Tibbles (bib82) 2007; 42 Frohlich, McCabe, Arnold, Day (bib70) 2008; 27 Chetram, Don-Salu-Hewage, Hinton (bib113) 2011; 410 Dong, Yuan, Wu, Wang, Fan, Miriyala, Lin, Yao, Shi, Kang, Lorkiewicz, St Clair, Hung, Evers, Zhou (bib123) 2013; 23 Yu, Lao, Teng, Li, Zhou, Wang, Guo, Deng, Chang, Wu, Liu, Chen, Lu, Cheng, Li, Su, Jiang, Li, Huang, Yi, Zou (bib102) 2018; 9 Wu, Harder, Wong, Lang, Zhang (bib122) 2015; 54 Meitzler, Makhlouf, Antony, Wu, Butcher, Jiang, Juhasz, Lu, Dahan, Jansen-Dürr, Pircher, Shah, Roy, Doroshow (bib35) 2017; 13 Arbiser, Petros, Klafter, Govindajaran, McLaughlin, Brown, Cohen, Moses, Kilroy, Arnold, Lambeth (bib32) 2002; 99 Jung, Yang, Kim, Kim, Kim, Yun, Park, Kim, Choe, Kang, Ha (bib131) 2008; 29 Höll, Koziel, Schäfer, Pircher, Pauck, Hermann, Klocker, Jansen-Dürr, Sampson (bib36) 2016; 55 Labiano, Palazón, Bolaños, Azpilikueta, Sánchez-Paulete, Morales-Kastresana, Quetglas, Perez-Gracia, Gúrpide, Rodriguez-Ruiz, Aznar, Jure-Kunkel, Berraondo, Melero (bib97) 2016; 5 Verschoor, Wilson, Verschoor, Singh (bib133) 2010; 5 Gonzalez-Donquiles, Alonso-Molero, Fernandez-Villa, Vilorio-Marqués, Molina, Martín (bib62) 2017; 12 Berra, Pagès, Pouysségur (bib88) 2000; 19 Shi, Viswanadhapalli, Friedrichs, Velagapudi, Szyndralewiez, Bansal, Bhat, Choudhury, Abboud (bib116) 2018; 8 Radisky, Levy, Littlepage, Liu, Nelson, Fata, Leake, Godden, Albertson, Nieto, Werb, Bissell (bib132) 2005; 436 Iseghohi, Omage (bib127) 2016; 3 Labiano, Palazon, Melero (bib99) 2015; 42 Gupta, Singh, Pochampally, Watabe, Mo (bib135) 2014; 5 Petros, Baumann, Ruiz-Pesini, Amin, Sun, Hall, Lim, Issa, Flanders, Hosseini, Marshall, Wallace (bib26) 2005; 102 Diebold, Petry, Hess, Görlach (bib39) 2010; 21 Bellezza, Scarpelli, Pizzo, Grottelli, Costanzi, Minelli (bib69) 2017; 8 Sabharwal, Schumacker (bib5) 2014; 14 Wickenden, Jin, Johnson, Gillings, Newson, Austin, Chell, Balmanno, Pritchard, Cook (bib108) 2008; 27 DeNicola, Karreth, Humpton, Gopinathan, Wei, Frese, Mangal, Yu, Yeo, Calhoun, Scrimieri, Winter, Hruban, Iacobuzio-Donahue, Kern, Blair, Tuveson (bib67) 2011; 475 Alirol, Martinou (bib17) 2006; 25 Tam, Gao, Leung, Ho (bib34) 2003; 163 Ju, Ying, Tian, Ling, Fu, Lu, Wu, Yang, Achreja, Chen, Zhuang, Wang, Nagrath, Yao, Hung, DePinho, Huang, Xu, Chiao (bib42) 2017; 8 Helfinger, Henke, Harenkamp, Walter, Epah, Penski, Mittelbronn, Schröder (bib47) 2016; 216 Ruffels, Griffin, Dickenson (bib137) 2004; 483 Lee, Ryu, Son, Seo, Kim, Jung, Song, Hwang, Ahn (bib73) 2016; 2016 Okoh, Felty, Parkash, Poppiti, Roy (bib106) 2013; 8 Zhang, Lan, Hou, Li, Fang, Yang, Zhang, Liu, Liu (bib44) 2014; 5 Chaudhary, Bhat, Kumar, Kumar, Kumar, Underwood, Koochekpour, Shourideh, Yadav, Dhar, Chandra (bib29) 2016; 114 Panieri, Santoro (bib3) 2016; 7 Yan, Liu, Pei, Chen, Li, Wang, Jin, Zhu, Wang, Liu (bib43) 2015; 26 Wang, Zhang, Dong, Nice, Huang, Wei (bib119) 2013; 4 Idelchik, Begley, Begley, Melendez (bib13) 2017 Dec; 47 Chang, Chen, Chou, Han, Chen, Yang, Huang, Lo (bib120) 2014; 74 Jastroch, Divakaruni, Mookerjee, Treberg, Brand (bib83) 2010; 47 Mitsuishi, Taguchi, Kawatani, Shibata, Nukiwa, Aburatani, Yamamoto, Motohashi (bib64) 2012; 22 Baca, Prandi, Lawrence, Mosquera, Romanel, Drier, Park, Kitabayashi, MacDonald, Ghandi Brar (10.1016/j.canlet.2019.03.020_bib33) 2003; 285 Lee (10.1016/j.canlet.2019.03.020_bib73) 2016; 2016 Chaudhary (10.1016/j.canlet.2019.03.020_bib29) 2016; 114 Jung (10.1016/j.canlet.2019.03.020_bib131) 2008; 29 Muller (10.1016/j.canlet.2019.03.020_bib4) 2000; 23 Zhong (10.1016/j.canlet.2019.03.020_bib86) 1998; 58 Hoogsteen (10.1016/j.canlet.2019.03.020_bib76) 2007; 19 Jajoo (10.1016/j.canlet.2019.03.020_bib48) 2009; 11 Chouaib (10.1016/j.canlet.2019.03.020_bib96) 2017; 36 ACS (10.1016/j.canlet.2019.03.020_bib1) 2018 Jin (10.1016/j.canlet.2019.03.020_bib143) 2014; 75 Yan (10.1016/j.canlet.2019.03.020_bib43) 2015; 26 Weinberg (10.1016/j.canlet.2019.03.020_bib22) 2010; 107 Casas (10.1016/j.canlet.2019.03.020_bib31) 2017 Labiano (10.1016/j.canlet.2019.03.020_bib97) 2016; 5 Ryoo (10.1016/j.canlet.2019.03.020_bib63) 2016; 2016 Cho (10.1016/j.canlet.2019.03.020_bib89) 2014; 74 Kumar (10.1016/j.canlet.2019.03.020_bib52) 2016; 22 Trojan (10.1016/j.canlet.2019.03.020_bib57) 2005; 25 Pelicano (10.1016/j.canlet.2019.03.020_bib140) 2009; 69 WHO (10.1016/j.canlet.2019.03.020_bib2) 2018 Khandrika (10.1016/j.canlet.2019.03.020_bib8) 2009; 282 Diebold (10.1016/j.canlet.2019.03.020_bib15) 2016; 100 Chetram (10.1016/j.canlet.2019.03.020_bib113) 2011; 410 Robinson (10.1016/j.canlet.2019.03.020_bib50) 2015; 161 Bell (10.1016/j.canlet.2019.03.020_bib16) 2011; 30 Kurkjian (10.1016/j.canlet.2019.03.020_bib129) 2008; 32 Lee (10.1016/j.canlet.2019.03.020_bib61) 2017; 31 Tas (10.1016/j.canlet.2019.03.020_bib85) 2005; 22 Ha (10.1016/j.canlet.2019.03.020_bib136) 2010; 16 Mitsuishi (10.1016/j.canlet.2019.03.020_bib64) 2012; 22 Wu (10.1016/j.canlet.2019.03.020_bib66) 2017; 352 Tan (10.1016/j.canlet.2019.03.020_bib117) 2018 Schumacker (10.1016/j.canlet.2019.03.020_bib11) 2015; 27 Arbiser (10.1016/j.canlet.2019.03.020_bib32) 2002; 99 Meitzler (10.1016/j.canlet.2019.03.020_bib35) 2017; 13 Balamurugan (10.1016/j.canlet.2019.03.020_bib91) 2013; 9 Khandrika (10.1016/j.canlet.2019.03.020_bib93) 2009; 28 Deep (10.1016/j.canlet.2019.03.020_bib37) 2016; 6 Whitaker (10.1016/j.canlet.2019.03.020_bib110) 2013; 109 Barnett (10.1016/j.canlet.2019.03.020_bib142) 2011; 404 Tafani (10.1016/j.canlet.2019.03.020_bib98) 2016; 2016 Simon (10.1016/j.canlet.2019.03.020_bib20) 2000; 5 Lu (10.1016/j.canlet.2019.03.020_bib141) 2017; 77 van de Schootbrugge (10.1016/j.canlet.2019.03.020_bib94) 2014; 14 Zhang (10.1016/j.canlet.2019.03.020_bib44) 2014; 5 Wickenden (10.1016/j.canlet.2019.03.020_bib108) 2008; 27 Alirol (10.1016/j.canlet.2019.03.020_bib17) 2006; 25 Porporato (10.1016/j.canlet.2019.03.020_bib23) 2015; 2 Iseghohi (10.1016/j.canlet.2019.03.020_bib127) 2016; 3 Frohlich (10.1016/j.canlet.2019.03.020_bib70) 2008; 27 Chen (10.1016/j.canlet.2019.03.020_bib27) 2003; 24 Moltzahn (10.1016/j.canlet.2019.03.020_bib124) 2013; 2 Gao (10.1016/j.canlet.2019.03.020_bib46) 2017; 9 Beltran (10.1016/j.canlet.2019.03.020_bib53) 2016; 22 DeNicola (10.1016/j.canlet.2019.03.020_bib67) 2011; 475 Yu (10.1016/j.canlet.2019.03.020_bib18) 2012; 57 Hasmim (10.1016/j.canlet.2019.03.020_bib100) 2015; 6 Shi (10.1016/j.canlet.2019.03.020_bib116) 2018; 8 Ju (10.1016/j.canlet.2019.03.020_bib42) 2017; 8 Berra (10.1016/j.canlet.2019.03.020_bib88) 2000; 19 Gupta (10.1016/j.canlet.2019.03.020_bib135) 2014; 5 Millar (10.1016/j.canlet.2019.03.020_bib82) 2007; 42 Baca (10.1016/j.canlet.2019.03.020_bib51) 2013; 153 Dey (10.1016/j.canlet.2019.03.020_bib19) 2000; 275 Kim (10.1016/j.canlet.2019.03.020_bib125) 2013; 33 Labiano (10.1016/j.canlet.2019.03.020_bib99) 2015; 42 Samaranayake (10.1016/j.canlet.2019.03.020_bib60) 2017; 8 Deep (10.1016/j.canlet.2019.03.020_bib103) 2015; 20 Yamaguchi (10.1016/j.canlet.2019.03.020_bib90) 2015; 88 Jastroch (10.1016/j.canlet.2019.03.020_bib83) 2010; 47 Taylor (10.1016/j.canlet.2019.03.020_bib49) 2010; 18 Kudryavtseva (10.1016/j.canlet.2019.03.020_bib126) 2016; 7 Diebold (10.1016/j.canlet.2019.03.020_bib39) 2010; 21 Bellezza (10.1016/j.canlet.2019.03.020_bib69) 2017; 8 Hamanaka (10.1016/j.canlet.2019.03.020_bib21) 2013; 6 Zulueta (10.1016/j.canlet.2019.03.020_bib84) 1995; 12 Shiota (10.1016/j.canlet.2019.03.020_bib7) 2011; 51 Diehn (10.1016/j.canlet.2019.03.020_bib118) 2009; 458 Chang (10.1016/j.canlet.2019.03.020_bib120) 2014; 74 Piskounova (10.1016/j.canlet.2019.03.020_bib59) 2015; 527 Helfinger (10.1016/j.canlet.2019.03.020_bib47) 2016; 216 Kumar (10.1016/j.canlet.2019.03.020_bib6) 2008; 68 Campisi (10.1016/j.canlet.2019.03.020_bib128) 2005; 120 Nogueira (10.1016/j.canlet.2019.03.020_bib144) 2008; 14 Chio (10.1016/j.canlet.2019.03.020_bib65) 2016; 166 Afanas'ev (10.1016/j.canlet.2019.03.020_bib130) 2014; 5 Sullivan (10.1016/j.canlet.2019.03.020_bib14) 2014; 2 Boudreau (10.1016/j.canlet.2019.03.020_bib114) 2012; 53 Farhan (10.1016/j.canlet.2019.03.020_bib107) 2017; 13 Bedard (10.1016/j.canlet.2019.03.020_bib30) 2007; 87 Idelchik (10.1016/j.canlet.2019.03.020_bib13) 2017; 47 Radisky (10.1016/j.canlet.2019.03.020_bib132) 2005; 436 Yoon (10.1016/j.canlet.2019.03.020_bib139) 2010; 6 Freitas (10.1016/j.canlet.2019.03.020_bib10) 2012; 2 Jessie (10.1016/j.canlet.2019.03.020_bib25) 2001; 37 Panieri (10.1016/j.canlet.2019.03.020_bib3) 2016; 7 Tam (10.1016/j.canlet.2019.03.020_bib34) 2003; 163 Armenia (10.1016/j.canlet.2019.03.020_bib55) 2018; 50 Oben (10.1016/j.canlet.2019.03.020_bib134) 2017; 8 Hai (10.1016/j.canlet.2019.03.020_bib95) 2017; 7 Okoh (10.1016/j.canlet.2019.03.020_bib106) 2013; 8 Dong (10.1016/j.canlet.2019.03.020_bib123) 2013; 23 Taniuchi (10.1016/j.canlet.2019.03.020_bib109) 2015; 44 Barbieri (10.1016/j.canlet.2019.03.020_bib56) 2012; 44 Schlaepfer (10.1016/j.canlet.2019.03.020_bib104) 2015; 6 Dolado (10.1016/j.canlet.2019.03.020_bib138) 2007; 11 Zhang (10.1016/j.canlet.2019.03.020_bib79) 2014; 2 Ruffels (10.1016/j.canlet.2019.03.020_bib137) 2004; 483 Luoto (10.1016/j.canlet.2019.03.020_bib74) 2013; 4 Loeb (10.1016/j.canlet.2019.03.020_bib9) 2000; 21 Liu (10.1016/j.canlet.2019.03.020_bib72) 2015; 41 Dakubo (10.1016/j.canlet.2019.03.020_bib24) 2006; 59 Sabharwal (10.1016/j.canlet.2019.03.020_bib5) 2014; 14 Sampson (10.1016/j.canlet.2019.03.020_bib41) 2011; 25 Balamurugan (10.1016/j.canlet.2019.03.020_bib87) 2016; 138 Petros (10.1016/j.canlet.2019.03.020_bib26) 2005; 102 Bristow (10.1016/j.canlet.2019.03.020_bib77) 2008; 8 Kim (10.1016/j.canlet.2019.03.020_bib121) 2012; 19 Wu (10.1016/j.canlet.2019.03.020_bib122) 2015; 54 Kumar (10.1016/j.canlet.2019.03.020_bib101) 2014; 143 Hong (10.1016/j.canlet.2019.03.020_bib78) 2016; 34 Paranjape (10.1016/j.canlet.2019.03.020_bib112) 2016; 35 Kalo (10.1016/j.canlet.2019.03.020_bib68) 2012; 125 Höll (10.1016/j.canlet.2019.03.020_bib36) 2016; 55 Verschoor (10.1016/j.canlet.2019.03.020_bib133) 2010; 5 Schultz (10.1016/j.canlet.2019.03.020_bib71) 2014; 9 Le (10.1016/j.canlet.2019.03.020_bib81) 2014; 111 Kim (10.1016/j.canlet.2019.03.020_bib45) 2017; 116 Dolado (10.1016/j.canlet.2019.03.020_bib145) 2008; 14 Ren (10.1016/j.canlet.2019.03.020_bib111) 2014; 5 Crosas-Molist (10.1016/j.canlet.2019.03.020_bib115) 2017; 36 Hanley (10.1016/j.canlet.2019.03.020_bib40) 2018; 110 Chandel (10.1016/j.canlet.2019.03.020_bib58) 2014; 371 Gonzalez-Donquiles (10.1016/j.canlet.2019.03.020_bib62) 2017; 12 Li (10.1016/j.canlet.2019.03.020_bib38) 2013; 1833 Network (10.1016/j.canlet.2019.03.020_bib54) 2015; 163 Yu (10.1016/j.canlet.2019.03.020_bib102) 2018; 9 Trédan (10.1016/j.canlet.2019.03.020_bib75) 2007; 99 Wang (10.1016/j.canlet.2019.03.020_bib119) 2013; 4 White (10.1016/j.canlet.2019.03.020_bib12) 2014; 46 Chen (10.1016/j.canlet.2019.03.020_bib28) 2002; 62 Kunz (10.1016/j.canlet.2019.03.020_bib80) 2003; 2 Li (10.1016/j.canlet.2019.03.020_bib105) 2016; 36 Sumbayev (10.1016/j.canlet.2019.03.020_bib92) 2005; 436 |
References_xml | – volume: 12 year: 2017 ident: bib62 article-title: The NRF2 transcription factor plays a dual role in colorectal cancer: a systematic review publication-title: PLoS One – volume: 30 start-page: 2986 year: 2011 end-page: 2996 ident: bib16 article-title: SirT3 suppresses hypoxia inducible factor 1α and tumor growth by inhibiting mitochondrial ROS production publication-title: Oncogene – year: 2017 ident: bib31 article-title: NOX4-dependent neuronal autotoxicity and BBB breakdown explain the superior sensitivity of the brain to ischemic damage publication-title: Proc Natl Acad Sci U S A – volume: 138 start-page: 1058 year: 2016 end-page: 1066 ident: bib87 article-title: HIF-1 at the crossroads of hypoxia, inflammation, and cancer publication-title: Int. J. Cancer – volume: 6 start-page: 482 year: 2015 ident: bib100 article-title: Critical role of tumor microenvironment in shaping NK cell functions: implication of hypoxic stress publication-title: Front. Immunol. – volume: 18 start-page: 11 year: 2010 end-page: 22 ident: bib49 article-title: Integrative genomic profiling of human prostate cancer publication-title: Cancer Cell – volume: 102 start-page: 719 year: 2005 end-page: 724 ident: bib26 article-title: mtDNA mutations increase tumorigenicity in prostate cancer publication-title: Proc. Natl. Acad. Sci. U.S.A. – volume: 2016 year: 2016 ident: bib73 article-title: TGF-β and hypoxia/reoxygenation promote radioresistance of A549 lung cancer cells through activation of Nrf2 and EGFR publication-title: Oxid Med Cell Longev – volume: 9 start-page: 3157 year: 2018 ident: bib102 article-title: SENP3 maintains the stability and function of regulatory T cells via BACH2 deSUMOylation publication-title: Nat. Commun. – volume: 5 start-page: 12070 year: 2014 end-page: 12082 ident: bib135 article-title: Acidosis promotes invasiveness of breast cancer cells through ROS-AKT-NF-κB pathway publication-title: Oncotarget – volume: 74 start-page: 528 year: 2014 end-page: 536 ident: bib89 article-title: A ROS/STAT3/HIF-1α signaling cascade mediates EGF-induced TWIST1 expression and prostate cancer cell invasion publication-title: Prostate – volume: 4 start-page: e537 year: 2013 ident: bib119 article-title: Redox homeostasis: the linchpin in stem cell self-renewal and differentiation publication-title: Cell Death Dis. – year: 2018 ident: bib2 article-title: Cancer Today – volume: 527 start-page: 186 year: 2015 end-page: 191 ident: bib59 article-title: Oxidative stress inhibits distant metastasis by human melanoma cells publication-title: Nature – volume: 2016 year: 2016 ident: bib98 article-title: The interplay of reactive oxygen species, hypoxia, inflammation, and sirtuins in cancer initiation and progression publication-title: Oxid Med Cell Longev – volume: 282 start-page: 125 year: 2009 end-page: 136 ident: bib8 article-title: Oxidative stress in prostate cancer publication-title: Cancer Lett. – volume: 8 start-page: 1204 year: 2017 ident: bib60 article-title: Thioredoxin-1 protects against androgen receptor-induced redox vulnerability in castration-resistant prostate cancer publication-title: Nat. Commun. – volume: 36 start-page: 439 year: 2017 end-page: 445 ident: bib96 article-title: Hypoxic stress: obstacles and opportunities for innovative immunotherapy of cancer publication-title: Oncogene – volume: 32 start-page: 187 year: 2008 end-page: 235 ident: bib129 article-title: DNA methylation: its role in cancer development and therapy publication-title: Curr. Probl. Cancer – volume: 153 start-page: 666 year: 2013 end-page: 677 ident: bib51 article-title: Punctuated evolution of prostate cancer genomes publication-title: Cell – volume: 36 start-page: 3002 year: 2017 end-page: 3014 ident: bib115 article-title: The NADPH oxidase NOX4 represses epithelial to amoeboid transition and efficient tumour dissemination publication-title: Oncogene – volume: 12 start-page: 41 year: 1995 end-page: 49 ident: bib84 article-title: Release of hydrogen peroxide in response to hypoxia-reoxygenation: role of an NAD(P)H oxidase-like enzyme in endothelial cell plasma membrane publication-title: Am. J. Respir. Cell Mol. Biol. – volume: 59 start-page: 10 year: 2006 end-page: 16 ident: bib24 article-title: Altered metabolism and mitochondrial genome in prostate cancer publication-title: J. Clin. Pathol. – volume: 69 start-page: 2375 year: 2009 end-page: 2383 ident: bib140 article-title: Mitochondrial dysfunction and reactive oxygen species imbalance promote breast cancer cell motility through a CXCL14-mediated mechanism publication-title: Cancer Res. – volume: 87 start-page: 245 year: 2007 end-page: 313 ident: bib30 article-title: The NOX family of ROS-generating NADPH oxidases: physiology and pathophysiology publication-title: Physiol. Rev. – volume: 216 start-page: 435 year: 2016 end-page: 446 ident: bib47 article-title: The NADPH Oxidase Nox4 mediates tumour angiogenesis publication-title: Acta Physiol. – volume: 6 start-page: 22836 year: 2015 end-page: 22856 ident: bib104 article-title: Hypoxia induces triglycerides accumulation in prostate cancer cells and extracellular vesicles supporting growth and invasiveness following reoxygenation publication-title: Oncotarget – volume: 110 year: 2018 ident: bib40 article-title: Targeting the myofibroblastic cancer-associated fibroblast phenotype through inhibition of NOX4 publication-title: J. Natl. Cancer Inst. – volume: 166 start-page: 963 year: 2016 end-page: 976 ident: bib65 article-title: NRF2 promotes tumor maintenance by modulating mRNA translation in pancreatic cancer publication-title: Cell – volume: 35 start-page: 5963 year: 2016 end-page: 5976 ident: bib112 article-title: Inhibition of FOXC2 restores epithelial phenotype and drug sensitivity in prostate cancer cells with stem-cell properties publication-title: Oncogene – volume: 3 start-page: 105 year: 2016 end-page: 109 ident: bib127 article-title: How ageing increases cancer susceptibility: a tale of two opposing yet synergistic views publication-title: Genes Dis – volume: 7 start-page: e2253 year: 2016 ident: bib3 article-title: ROS homeostasis and metabolism: a dangerous liaison in cancer cells publication-title: Cell Death & Disease – volume: 19 start-page: S539 year: 2012 end-page: S548 ident: bib121 article-title: Increased CD13 expression reduces reactive oxygen species, promoting survival of liver cancer stem cells via an epithelial-mesenchymal transition-like phenomenon publication-title: Ann. Surg. Oncol. – volume: 2 start-page: 17 year: 2014 ident: bib14 article-title: Mitochondrial reactive oxygen species and cancer publication-title: Cancer Metabol. – volume: 44 start-page: 331 year: 2015 end-page: 340 ident: bib109 article-title: Peroxiredoxin 1 promotes pancreatic cancer cell invasion by modulating p38 MAPK activity publication-title: Pancreas – volume: 5 start-page: 415 year: 2000 end-page: 418 ident: bib20 article-title: Role of reactive oxygen species (ROS) in apoptosis induction publication-title: Apoptosis – volume: 68 start-page: 1777 year: 2008 end-page: 1785 ident: bib6 article-title: Oxidative stress is inherent in prostate cancer cells and is required for aggressive phenotype publication-title: Cancer Res. – volume: 14 start-page: 427 year: 2008 end-page: 429 ident: bib145 article-title: AKT and oxidative stress team up to kill cancer cells publication-title: Cancer Cell – volume: 21 start-page: 379 year: 2000 end-page: 385 ident: bib9 article-title: Significance of multiple mutations in cancer publication-title: Carcinogenesis – volume: 99 start-page: 715 year: 2002 end-page: 720 ident: bib32 article-title: Reactive oxygen generated by Nox1 triggers the angiogenic switch publication-title: Proc. Natl. Acad. Sci. U. S. A. – volume: 2 start-page: 242 year: 2013 end-page: 253 ident: bib124 article-title: Cancer stem cells in prostate cancer publication-title: Transl. Androl. Urol. – volume: 36 start-page: 521 year: 2016 end-page: 527 ident: bib105 article-title: Hypoxia inducible factor-1α-dependent epithelial to mesenchymal transition under hypoxic conditions in prostate cancer cells publication-title: Oncol. Rep. – volume: 436 start-page: 123 year: 2005 end-page: 127 ident: bib132 article-title: Rac1b and reactive oxygen species mediate MMP-3-induced EMT and genomic instability publication-title: Nature – volume: 14 start-page: 709 year: 2014 end-page: 721 ident: bib5 article-title: Mitochondrial ROS in cancer: initiators, amplifiers or an Achilles' heel? publication-title: Nat. Rev. Canc. – volume: 22 start-page: 369 year: 2016 end-page: 378 ident: bib52 article-title: Substantial interindividual and limited intraindividual genomic diversity among tumors from men with metastatic prostate cancer publication-title: Nat. Med. – volume: 27 start-page: 156 year: 2015 end-page: 157 ident: bib11 article-title: Reactive oxygen species in cancer: a dance with the devil publication-title: Cancer Cell – volume: 11 start-page: 1132 year: 2009 end-page: 1145 ident: bib48 article-title: Adenosine A(3) receptor suppresses prostate cancer metastasis by inhibiting NADPH oxidase activity publication-title: Neoplasia – volume: 4 year: 2013 ident: bib74 article-title: Tumor hypoxia as a driving force in genetic instability publication-title: Genome Integr. – volume: 53 start-page: 1489 year: 2012 end-page: 1499 ident: bib114 article-title: Nox4 involvement in TGF-beta and SMAD3-driven induction of the epithelial-to-mesenchymal transition and migration of breast epithelial cells publication-title: Free Radic. Biol. Med. – volume: 41 start-page: 52 year: 2015 end-page: 57 ident: bib72 article-title: Nrf2 sensitizes prostate cancer cells to radiation via decreasing basal ROS levels publication-title: Biofactors – volume: 22 start-page: 298 year: 2016 end-page: 305 ident: bib53 article-title: Divergent clonal evolution of castration-resistant neuroendocrine prostate cancer publication-title: Nat. Med. – volume: 46 start-page: S7 year: 2014 end-page: S15 ident: bib12 article-title: Age and cancer risk: a potentially modifiable relationship publication-title: Am. J. Prev. Med. – volume: 114 start-page: 1090 year: 2016 end-page: 1100 ident: bib29 article-title: Mitochondrial dysfunction-mediated apoptosis resistance associates with defective heat shock protein response in African-American men with prostate cancer publication-title: Br. J. Canc. – volume: 143 start-page: 512 year: 2014 end-page: 519 ident: bib101 article-title: Hypoxia-inducible factors in regulation of immune responses in tumour microenvironment publication-title: Immunology – volume: 285 start-page: C353 year: 2003 end-page: C369 ident: bib33 article-title: Oxidase regulates growth and apoptosis in DU 145 prostate cancer cells publication-title: Am. J. Physiol. Cell Physiol. – volume: 25 start-page: 503 year: 2011 end-page: 515 ident: bib41 article-title: ROS signaling by NOX4 drives fibroblast-to-myofibroblast differentiation in the diseased prostatic stroma publication-title: Mol. Endocrinol. – volume: 107 start-page: 8788 year: 2010 end-page: 8793 ident: bib22 article-title: Mitochondrial metabolism and ROS generation are essential for Kras-mediated tumorigenicity publication-title: Proc. Natl. Acad. Sci. U. S. A. – volume: 21 start-page: 2087 year: 2010 end-page: 2096 ident: bib39 article-title: The NADPH oxidase subunit NOX4 is a new target gene of the hypoxia-inducible factor-1 publication-title: Mol. Biol. Cell – volume: 9 start-page: 917 year: 2013 end-page: 933 ident: bib91 article-title: The many faces of C/EBPδ and their relevance for inflammation and cancer publication-title: Int. J. Biol. Sci. – volume: 458 start-page: 780 year: 2009 end-page: 783 ident: bib118 article-title: Association of reactive oxygen species levels and radioresistance in cancer stem cells publication-title: Nature – volume: 75 start-page: S34 year: 2014 end-page: S35 ident: bib143 article-title: Reactive oxygen species and PI3K/Akt signaling in cancer publication-title: Free Radic. Biol. Med. – volume: 125 start-page: 5578 year: 2012 end-page: 5586 ident: bib68 article-title: Mutant p53R273H attenuates the expression of phase 2 detoxifying enzymes and promotes the survival of cells with high levels of reactive oxygen species publication-title: J. Cell Sci. – volume: 5 start-page: 52 year: 2014 end-page: 62 ident: bib130 article-title: New nucleophilic mechanisms of ros-dependent epigenetic modifications: comparison of aging and cancer publication-title: Aging Dis – volume: 31 start-page: 1608 year: 2017 end-page: 1619 ident: bib61 article-title: Endostatin inhibits androgen-independent prostate cancer growth by suppressing nuclear receptor-mediated oxidative stress publication-title: FASEB J. – volume: 8 start-page: 77436 year: 2017 end-page: 77452 ident: bib134 article-title: Oxidative stress-induced JNK/AP-1 signaling is a major pathway involved in selective apoptosis of myelodysplastic syndrome cells by with aferin-A publication-title: Oncotarget – volume: 47 start-page: 57 year: 2017 Dec end-page: 66 ident: bib13 article-title: Mitochondrial ROS control of cancer publication-title: Semin. Canc. Biol. – volume: 5 year: 2016 ident: bib97 article-title: Hypoxia-induced soluble CD137 in malignant cells blocks CD137L-costimulation as an immune escape mechanism publication-title: OncoImmunology – volume: 404 start-page: 34 year: 2011 end-page: 39 ident: bib142 article-title: Snail-mediated regulation of reactive oxygen species in ARCaP human prostate cancer cells publication-title: Biochem. Biophys. Res. Commun. – volume: 436 start-page: 406 year: 2005 end-page: 412 ident: bib92 article-title: Regulation of MAP kinase-dependent apoptotic pathway: implication of reactive oxygen and nitrogen species publication-title: Arch. Biochem. Biophys. – volume: 99 start-page: 1441 year: 2007 end-page: 1454 ident: bib75 article-title: Drug resistance and the solid tumor microenvironment publication-title: J. Natl. Cancer Inst. – volume: 2016 year: 2016 ident: bib63 article-title: Redox modulating NRF2: a potential mediator of cancer stem cell resistance publication-title: Oxid Med Cell Longev – volume: 22 start-page: 11 year: 2005 end-page: 15 ident: bib85 article-title: Oxidative stress in breast cancer publication-title: Med. Oncol. – volume: 34 start-page: 239 year: 2016 end-page: 249 ident: bib78 article-title: Tumor hypoxia and reoxygenation: the yin and yang for radiotherapy publication-title: Radiation Oncology Journal – volume: 20 start-page: 419 year: 2015 end-page: 434 ident: bib103 article-title: Hypoxia-induced signaling promotes prostate cancer progression: exosomes role as messenger of hypoxic response in tumor microenvironment publication-title: Crit. Rev. Oncog. – volume: 275 start-page: 7087 year: 2000 end-page: 7094 ident: bib19 article-title: Lack of oxidative phosphorylation and low mitochondrial membrane potential decrease susceptibility to apoptosis and do not modulate the protective effect of Bcl-x(L) in osteosarcoma cells publication-title: J. Biol. Chem. – volume: 8 start-page: 180 year: 2008 end-page: 192 ident: bib77 article-title: Hypoxia and metabolism. Hypoxia, DNA repair and genetic instability publication-title: Nat. Rev. Canc. – volume: 8 start-page: 3781 year: 2018 ident: bib116 article-title: Nox4 is a target for tuberin deficiency syndrome publication-title: Sci. Rep. – volume: 44 start-page: 685 year: 2012 end-page: 689 ident: bib56 article-title: Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer publication-title: Nat. Genet. – volume: 483 start-page: 163 year: 2004 end-page: 173 ident: bib137 article-title: Activation of ERK1/2, JNK and PKB by hydrogen peroxide in human SH-SY5Y neuroblastoma cells: role of ERK1/2 in H2O2-induced cell death publication-title: Eur. J. Pharmacol. – volume: 116 start-page: 370 year: 2017 end-page: 381 ident: bib45 article-title: Regulation of anoikis resistance by NADPH oxidase 4 and epidermal growth factor receptor publication-title: Br. J. Canc. – volume: 58 start-page: 5280 year: 1998 end-page: 5284 ident: bib86 article-title: Increased expression of hypoxia inducible factor-1alpha in rat and human prostate cancer publication-title: Cancer Res. – volume: 42 start-page: 378 year: 2015 end-page: 386 ident: bib99 article-title: Immune response regulation in the tumor microenvironment by hypoxia publication-title: Semin. Oncol. – volume: 7 start-page: 44879 year: 2016 end-page: 44905 ident: bib126 article-title: Mitochondrial dysfunction and oxidative stress in aging and cancer publication-title: Oncotarget – volume: 50 start-page: 645 year: 2018 end-page: 651 ident: bib55 article-title: The long tail of oncogenic drivers in prostate cancer publication-title: Nat. Genet. – volume: 9 year: 2014 ident: bib71 article-title: Nrf1 and Nrf2 transcription factors regulate androgen receptor transactivation in prostate cancer cells publication-title: PLoS One – volume: 163 start-page: 1011 year: 2015 end-page: 1025 ident: bib54 article-title: The molecular taxonomy of primary prostate cancer publication-title: Cell – volume: 47 start-page: 53 year: 2010 end-page: 67 ident: bib83 article-title: Mitochondrial proton and electron leaks publication-title: Essays Biochem. – volume: 8 start-page: 14437 year: 2017 ident: bib42 article-title: Mutant Kras- and p16-regulated NOX4 activation overcomes metabolic checkpoints in development of pancreatic ductal adenocarcinoma publication-title: Nat. Commun. – volume: 22 start-page: 66 year: 2012 end-page: 79 ident: bib64 article-title: Nrf2 redirects glucose and glutamine into anabolic pathways in metabolic reprogramming publication-title: Cancer Cell – volume: 371 start-page: 177 year: 2014 end-page: 178 ident: bib58 article-title: The promise and perils of antioxidants for cancer patients publication-title: N. Engl. J. Med. – volume: 13 start-page: 815 year: 2017 end-page: 827 ident: bib107 article-title: FOXO signaling pathways as therapeutic targets in cancer publication-title: Int. J. Biol. Sci. – volume: 5 start-page: 7093 year: 2014 end-page: 7104 ident: bib111 article-title: De-SUMOylation of FOXC2 by SENP3 promotes the epithelial-mesenchymal transition in gastric cancer cells publication-title: Oncotarget – volume: 19 start-page: 385 year: 2007 end-page: 396 ident: bib76 article-title: The hypoxic tumour microenvironment, patient selection and hypoxia-modifying treatments publication-title: Clin. Oncol. – volume: 19 start-page: 139 year: 2000 end-page: 145 ident: bib88 article-title: MAP kinases and hypoxia in the control of VEGF expression publication-title: Cancer Metastasis Rev. – volume: 25 start-page: 4706 year: 2006 end-page: 4716 ident: bib17 article-title: Mitochondria and cancer: is there a morphological connection? publication-title: Oncogene – volume: 8 start-page: 67506 year: 2017 end-page: 67518 ident: bib69 article-title: ROS-independent Nrf2 activation in prostate cancer publication-title: Oncotarget – volume: 74 start-page: 6291 year: 2014 end-page: 6305 ident: bib120 article-title: Distinct subpopulations of head and neck cancer cells with different levels of intracellular reactive oxygen species exhibit diverse stemness, proliferation, and chemosensitivity publication-title: Cancer Res. – volume: 6 start-page: 1125 year: 2010 end-page: 1138 ident: bib139 article-title: STAT3 transcriptional factor activated by reactive oxygen species induces IL6 in starvation-induced autophagy of cancer cells publication-title: Autophagy – volume: 5 year: 2010 ident: bib133 article-title: Ets-1 regulates energy metabolism in cancer cells publication-title: PLoS One – volume: 62 start-page: 6470 year: 2002 end-page: 6474 ident: bib28 article-title: Extensive somatic mitochondrial mutations in primary prostate cancer using laser capture microdissection publication-title: Cancer Res. – volume: 5 start-page: 4392 year: 2014 end-page: 4405 ident: bib44 article-title: NOX4 promotes non-small cell lung cancer cell proliferation and metastasis through positive feedback regulation of PI3K/Akt signaling publication-title: Oncotarget – volume: 161 start-page: 1215 year: 2015 end-page: 1228 ident: bib50 article-title: Integrative clinical genomics of advanced prostate cancer publication-title: Cell – volume: 88 start-page: 262 year: 2015 end-page: 275 ident: bib90 article-title: Inflammation and hypoxia linked to renal injury by CCAAT/enhancer-binding protein δ publication-title: Kidney Int. – volume: 2 start-page: 119 year: 2012 end-page: 128 ident: bib10 article-title: Oxidative stress adaptation in aggressive prostate cancer may be counteracted by the reduction of glutathione reductase publication-title: FEBS Open Bio – volume: 33 start-page: 4469 year: 2013 end-page: 4474 ident: bib125 article-title: Low production of reactive oxygen species and high DNA repair: mechanism of radioresistance of prostate cancer stem cells publication-title: Anticancer Res. – volume: 163 start-page: 2513 year: 2003 end-page: 2522 ident: bib34 article-title: Androgenic regulation of oxidative stress in the rat prostate: involvement of NAD(P)H oxidases and antioxidant defense machinery during prostatic involution and regrowth publication-title: Am. J. Pathol. – volume: 410 start-page: 195 year: 2011 end-page: 200 ident: bib113 article-title: ROS enhances CXCR4-mediated functions through inactivation of PTEN in prostate cancer cells publication-title: Biochem. Biophys. Res. Commun. – volume: 37 start-page: 169 year: 2001 end-page: 174 ident: bib25 article-title: Accumulation of mitochondrial DNA deletions in the malignant prostate of patients of different ages publication-title: Exp. Gerontol. – volume: 475 start-page: 106 year: 2011 end-page: 109 ident: bib67 article-title: Oncogene-induced Nrf2 transcription promotes ROS detoxification and tumorigenesis publication-title: Nature – volume: 28 start-page: 1248 year: 2009 end-page: 1260 ident: bib93 article-title: Hypoxia-associated p38 mitogen-activated protein kinase-mediated androgen receptor activation and increased HIF-1alpha levels contribute to emergence of an aggressive phenotype in prostate cancer publication-title: Oncogene – volume: 23 start-page: 316 year: 2013 end-page: 331 ident: bib123 article-title: Loss of FBP1 by Snail-mediated repression provides metabolic advantages in basal-like breast cancer publication-title: Cancer Cell – volume: 2 year: 2015 ident: bib23 article-title: Paving the way for therapeutic prevention of tumor metastasis with agents targeting mitochondrial superoxide publication-title: Mol Cell Oncol – volume: 14 start-page: 252 year: 2014 ident: bib94 article-title: Effect of hypoxia on the expression of αB-crystallin in head and neck squamous cell carcinoma publication-title: BMC Canc. – year: 2018 ident: bib1 article-title: Cancer Facts & Figures 2018 – volume: 2 start-page: 23 year: 2003 ident: bib80 article-title: Molecular responses to hypoxia in tumor cells publication-title: Mol. Canc. – volume: 11 start-page: 191 year: 2007 end-page: 205 ident: bib138 article-title: p38alpha MAP kinase as a sensor of reactive oxygen species in tumorigenesis publication-title: Cancer Cell – volume: 6 start-page: 23135 year: 2016 ident: bib37 article-title: Graviola inhibits hypoxia-induced NADPH oxidase activity in prostate cancer cells reducing their proliferation and clonogenicity publication-title: Sci. Rep. – volume: 109 start-page: 983 year: 2013 end-page: 993 ident: bib110 article-title: Peroxiredoxin-3 is overexpressed in prostate cancer and promotes cancer cell survival by protecting cells from oxidative stress publication-title: Br. J. Canc. – volume: 7 start-page: 39692 year: 2017 ident: bib95 article-title: TRIM14 is a putative tumor suppressor and regulator of innate immune response in non-small cell lung cancer publication-title: Sci. Rep. – volume: 6 start-page: ra8 year: 2013 ident: bib21 article-title: Mitochondrial reactive oxygen species promote epidermal differentiation and hair follicle development publication-title: Sci. Signal. – volume: 352 start-page: 245 year: 2017 end-page: 254 ident: bib66 article-title: Nrf2 mediates redox adaptation in NOX4-overexpressed non-small cell lung cancer cells publication-title: Exp. Cell Res. – volume: 57 start-page: 99 year: 2012 end-page: 138 ident: bib18 article-title: Somatic mitochondrial DNA mutations in human cancers publication-title: Adv. Clin. Chem. – volume: 1833 start-page: 3375 year: 2013 end-page: 3385 ident: bib38 article-title: NADPH oxidase subunit p22(phox)-mediated reactive oxygen species contribute to angiogenesis and tumor growth through AKT and ERK1/2 signaling pathways in prostate cancer publication-title: Biochim. Biophys. Acta – volume: 26 start-page: 388 year: 2015 end-page: 398 ident: bib43 article-title: Inhibition of NADPH oxidase protects against metastasis of human lung cancer by decreasing microRNA-21 publication-title: Anti Canccer Drugs – volume: 14 start-page: 458 year: 2008 end-page: 470 ident: bib144 article-title: Akt determines replicative senescence and oxidative or oncogenic premature senescence and sensitizes cells to oxidative apoptosis publication-title: Cancer Cell – volume: 24 start-page: 1481 year: 2003 end-page: 1487 ident: bib27 article-title: Simultaneous generation of multiple mitochondrial DNA mutations in human prostate tumors suggests mitochondrial hyper-mutagenesis publication-title: Carcinogenesis – volume: 51 start-page: 1320 year: 2011 end-page: 1328 ident: bib7 article-title: Oxidative stress and androgen receptor signaling in the development and progression of castration-resistant prostate cancer publication-title: Free Radic. Biol. Med. – volume: 100 start-page: 86 year: 2016 end-page: 93 ident: bib15 article-title: Mitochondrial ROS regulation of proliferating cells publication-title: Free Radic. Biol. Med. – volume: 25 start-page: 183 year: 2005 end-page: 191 ident: bib57 article-title: Identification of metastasis-associated genes in prostate cancer by genetic profiling of human prostate cancer cell lines publication-title: Anticancer Res. – volume: 16 start-page: 4932 year: 2010 end-page: 4937 ident: bib136 article-title: HBx-induced reactive oxygen species activates hepatocellular carcinogenesis via dysregulation of PTEN/Akt pathway publication-title: World J. Gastroenterol. – volume: 77 start-page: 2881 year: 2017 end-page: 2892 ident: bib141 article-title: NRF2 induction supporting breast cancer cell survival is enabled by oxidative stress-induced DPP3-KEAP1 interaction publication-title: Cancer Res. – volume: 111 start-page: 12486 year: 2014 end-page: 12491 ident: bib81 article-title: Tumorigenicity of hypoxic respiring cancer cells revealed by a hypoxia-cell cycle dual reporter publication-title: Proc. Natl. Acad. Sci. U. S. A. – volume: 2 start-page: 85 year: 2014 end-page: 99 ident: bib79 article-title: Population dynamics inside cancer biomass driven by repeated hypoxia-reoxygenation cycles publication-title: Quantitative Biology – volume: 54 start-page: 1494 year: 2015 end-page: 1502 ident: bib122 article-title: Oxidative stress, mammospheres and Nrf2-new implication for breast cancer therapy? publication-title: Mol. Carcinog. – volume: 120 start-page: 513 year: 2005 end-page: 522 ident: bib128 article-title: Senescent cells, tumor suppression, and organismal aging: good citizens, bad neighbors publication-title: Cell – volume: 13 start-page: 182 year: 2017 end-page: 195 ident: bib35 article-title: Decoding NADPH oxidase 4 expression in human tumors publication-title: Redox Biol – volume: 9 start-page: 4440 year: 2017 end-page: 4449 ident: bib46 article-title: RNAi-mediated silencing of NOX4 inhibited the invasion of gastric cancer cells through JAK2/STAT3 signaling publication-title: Am J Transl Res – volume: 27 start-page: 4353 year: 2008 end-page: 4362 ident: bib70 article-title: The role of Nrf2 in increased reactive oxygen species and DNA damage in prostate tumorigenesis publication-title: Oncogene – volume: 42 start-page: 1165 year: 2007 end-page: 1177 ident: bib82 article-title: ROS generation in endothelial hypoxia and reoxygenation stimulates MAP kinase signaling and kinase-dependent neutrophil recruitment publication-title: Free Radic. Biol. Med. – volume: 27 start-page: 7150 year: 2008 end-page: 7161 ident: bib108 article-title: Colorectal cancer cells with the BRAF(V600E) mutation are addicted to the ERK1/2 pathway for growth factor-independent survival and repression of BIM publication-title: Oncogene – volume: 8 start-page: e54206 year: 2013 ident: bib106 article-title: Reactive oxygen species via redox signaling to PI3K/AKT pathway contribute to the malignant growth of 4-hydroxy estradiol-transformed mammary epithelial cells publication-title: PLoS One – year: 2018 ident: bib117 article-title: ROS release by PPARβ/δ-null fibroblasts reduces tumor load through epithelial antioxidant response publication-title: Oncogene – volume: 29 start-page: 713 year: 2008 end-page: 721 ident: bib131 article-title: Reactive oxygen species stabilize hypoxia-inducible factor-1 alpha protein and stimulate transcriptional activity via AMP-activated protein kinase in DU145 human prostate cancer cells publication-title: Carcinogenesis – volume: 23 start-page: 227 year: 2000 end-page: 253 ident: bib4 article-title: The nature and mechanism of superoxide production by the electron transport chain: its relevance to aging publication-title: J Am Aging Assoc – volume: 55 start-page: 27 year: 2016 end-page: 39 ident: bib36 article-title: ROS signaling by NADPH oxidase 5 modulates the proliferation and survival of prostate carcinoma cells publication-title: Mol. Carcinog. – volume: 32 start-page: 187 year: 2008 ident: 10.1016/j.canlet.2019.03.020_bib129 article-title: DNA methylation: its role in cancer development and therapy publication-title: Curr. Probl. Cancer doi: 10.1016/j.currproblcancer.2008.08.002 – volume: 22 start-page: 369 year: 2016 ident: 10.1016/j.canlet.2019.03.020_bib52 article-title: Substantial interindividual and limited intraindividual genomic diversity among tumors from men with metastatic prostate cancer publication-title: Nat. Med. doi: 10.1038/nm.4053 – volume: 54 start-page: 1494 year: 2015 ident: 10.1016/j.canlet.2019.03.020_bib122 article-title: Oxidative stress, mammospheres and Nrf2-new implication for breast cancer therapy? publication-title: Mol. Carcinog. doi: 10.1002/mc.22202 – volume: 9 start-page: 4440 year: 2017 ident: 10.1016/j.canlet.2019.03.020_bib46 article-title: RNAi-mediated silencing of NOX4 inhibited the invasion of gastric cancer cells through JAK2/STAT3 signaling publication-title: Am J Transl Res – volume: 5 start-page: 52 year: 2014 ident: 10.1016/j.canlet.2019.03.020_bib130 article-title: New nucleophilic mechanisms of ros-dependent epigenetic modifications: comparison of aging and cancer publication-title: Aging Dis – volume: 58 start-page: 5280 year: 1998 ident: 10.1016/j.canlet.2019.03.020_bib86 article-title: Increased expression of hypoxia inducible factor-1alpha in rat and human prostate cancer publication-title: Cancer Res. – volume: 11 start-page: 191 year: 2007 ident: 10.1016/j.canlet.2019.03.020_bib138 article-title: p38alpha MAP kinase as a sensor of reactive oxygen species in tumorigenesis publication-title: Cancer Cell doi: 10.1016/j.ccr.2006.12.013 – volume: 8 start-page: 77436 year: 2017 ident: 10.1016/j.canlet.2019.03.020_bib134 article-title: Oxidative stress-induced JNK/AP-1 signaling is a major pathway involved in selective apoptosis of myelodysplastic syndrome cells by with aferin-A publication-title: Oncotarget doi: 10.18632/oncotarget.20497 – volume: 102 start-page: 719 year: 2005 ident: 10.1016/j.canlet.2019.03.020_bib26 article-title: mtDNA mutations increase tumorigenicity in prostate cancer publication-title: Proc. Natl. Acad. Sci. U.S.A. doi: 10.1073/pnas.0408894102 – volume: 161 start-page: 1215 year: 2015 ident: 10.1016/j.canlet.2019.03.020_bib50 article-title: Integrative clinical genomics of advanced prostate cancer publication-title: Cell doi: 10.1016/j.cell.2015.05.001 – volume: 8 start-page: 1204 year: 2017 ident: 10.1016/j.canlet.2019.03.020_bib60 article-title: Thioredoxin-1 protects against androgen receptor-induced redox vulnerability in castration-resistant prostate cancer publication-title: Nat. Commun. doi: 10.1038/s41467-017-01269-x – volume: 75 start-page: S34 issue: Suppl 1 year: 2014 ident: 10.1016/j.canlet.2019.03.020_bib143 article-title: Reactive oxygen species and PI3K/Akt signaling in cancer publication-title: Free Radic. Biol. Med. doi: 10.1016/j.freeradbiomed.2014.10.773 – volume: 7 start-page: e2253 year: 2016 ident: 10.1016/j.canlet.2019.03.020_bib3 article-title: ROS homeostasis and metabolism: a dangerous liaison in cancer cells publication-title: Cell Death & Disease doi: 10.1038/cddis.2016.105 – volume: 74 start-page: 528 year: 2014 ident: 10.1016/j.canlet.2019.03.020_bib89 article-title: A ROS/STAT3/HIF-1α signaling cascade mediates EGF-induced TWIST1 expression and prostate cancer cell invasion publication-title: Prostate doi: 10.1002/pros.22776 – volume: 33 start-page: 4469 year: 2013 ident: 10.1016/j.canlet.2019.03.020_bib125 article-title: Low production of reactive oxygen species and high DNA repair: mechanism of radioresistance of prostate cancer stem cells publication-title: Anticancer Res. – year: 2018 ident: 10.1016/j.canlet.2019.03.020_bib1 – volume: 21 start-page: 2087 year: 2010 ident: 10.1016/j.canlet.2019.03.020_bib39 article-title: The NADPH oxidase subunit NOX4 is a new target gene of the hypoxia-inducible factor-1 publication-title: Mol. Biol. Cell doi: 10.1091/mbc.e09-12-1003 – volume: 42 start-page: 1165 year: 2007 ident: 10.1016/j.canlet.2019.03.020_bib82 article-title: ROS generation in endothelial hypoxia and reoxygenation stimulates MAP kinase signaling and kinase-dependent neutrophil recruitment publication-title: Free Radic. Biol. Med. doi: 10.1016/j.freeradbiomed.2007.01.015 – volume: 1833 start-page: 3375 year: 2013 ident: 10.1016/j.canlet.2019.03.020_bib38 article-title: NADPH oxidase subunit p22(phox)-mediated reactive oxygen species contribute to angiogenesis and tumor growth through AKT and ERK1/2 signaling pathways in prostate cancer publication-title: Biochim. Biophys. Acta doi: 10.1016/j.bbamcr.2013.09.018 – volume: 125 start-page: 5578 year: 2012 ident: 10.1016/j.canlet.2019.03.020_bib68 article-title: Mutant p53R273H attenuates the expression of phase 2 detoxifying enzymes and promotes the survival of cells with high levels of reactive oxygen species publication-title: J. Cell Sci. – volume: 285 start-page: C353 year: 2003 ident: 10.1016/j.canlet.2019.03.020_bib33 article-title: Oxidase regulates growth and apoptosis in DU 145 prostate cancer cells publication-title: Am. J. Physiol. Cell Physiol. doi: 10.1152/ajpcell.00525.2002 – volume: 111 start-page: 12486 year: 2014 ident: 10.1016/j.canlet.2019.03.020_bib81 article-title: Tumorigenicity of hypoxic respiring cancer cells revealed by a hypoxia-cell cycle dual reporter publication-title: Proc. Natl. Acad. Sci. U. S. A. doi: 10.1073/pnas.1402012111 – volume: 5 year: 2010 ident: 10.1016/j.canlet.2019.03.020_bib133 article-title: Ets-1 regulates energy metabolism in cancer cells publication-title: PLoS One doi: 10.1371/journal.pone.0013565 – volume: 6 start-page: ra8 year: 2013 ident: 10.1016/j.canlet.2019.03.020_bib21 article-title: Mitochondrial reactive oxygen species promote epidermal differentiation and hair follicle development publication-title: Sci. Signal. doi: 10.1126/scisignal.2003638 – volume: 8 start-page: e54206 year: 2013 ident: 10.1016/j.canlet.2019.03.020_bib106 article-title: Reactive oxygen species via redox signaling to PI3K/AKT pathway contribute to the malignant growth of 4-hydroxy estradiol-transformed mammary epithelial cells publication-title: PLoS One doi: 10.1371/journal.pone.0054206 – volume: 88 start-page: 262 year: 2015 ident: 10.1016/j.canlet.2019.03.020_bib90 article-title: Inflammation and hypoxia linked to renal injury by CCAAT/enhancer-binding protein δ publication-title: Kidney Int. doi: 10.1038/ki.2015.21 – volume: 77 start-page: 2881 year: 2017 ident: 10.1016/j.canlet.2019.03.020_bib141 article-title: NRF2 induction supporting breast cancer cell survival is enabled by oxidative stress-induced DPP3-KEAP1 interaction publication-title: Cancer Res. doi: 10.1158/0008-5472.CAN-16-2204 – volume: 11 start-page: 1132 year: 2009 ident: 10.1016/j.canlet.2019.03.020_bib48 article-title: Adenosine A(3) receptor suppresses prostate cancer metastasis by inhibiting NADPH oxidase activity publication-title: Neoplasia doi: 10.1593/neo.09744 – volume: 6 start-page: 23135 year: 2016 ident: 10.1016/j.canlet.2019.03.020_bib37 article-title: Graviola inhibits hypoxia-induced NADPH oxidase activity in prostate cancer cells reducing their proliferation and clonogenicity publication-title: Sci. Rep. doi: 10.1038/srep23135 – volume: 3 start-page: 105 year: 2016 ident: 10.1016/j.canlet.2019.03.020_bib127 article-title: How ageing increases cancer susceptibility: a tale of two opposing yet synergistic views publication-title: Genes Dis doi: 10.1016/j.gendis.2016.04.002 – volume: 6 start-page: 1125 year: 2010 ident: 10.1016/j.canlet.2019.03.020_bib139 article-title: STAT3 transcriptional factor activated by reactive oxygen species induces IL6 in starvation-induced autophagy of cancer cells publication-title: Autophagy doi: 10.4161/auto.6.8.13547 – volume: 2 start-page: 119 year: 2012 ident: 10.1016/j.canlet.2019.03.020_bib10 article-title: Oxidative stress adaptation in aggressive prostate cancer may be counteracted by the reduction of glutathione reductase publication-title: FEBS Open Bio doi: 10.1016/j.fob.2012.05.001 – volume: 35 start-page: 5963 year: 2016 ident: 10.1016/j.canlet.2019.03.020_bib112 article-title: Inhibition of FOXC2 restores epithelial phenotype and drug sensitivity in prostate cancer cells with stem-cell properties publication-title: Oncogene doi: 10.1038/onc.2015.498 – volume: 27 start-page: 4353 year: 2008 ident: 10.1016/j.canlet.2019.03.020_bib70 article-title: The role of Nrf2 in increased reactive oxygen species and DNA damage in prostate tumorigenesis publication-title: Oncogene doi: 10.1038/onc.2008.79 – volume: 51 start-page: 1320 year: 2011 ident: 10.1016/j.canlet.2019.03.020_bib7 article-title: Oxidative stress and androgen receptor signaling in the development and progression of castration-resistant prostate cancer publication-title: Free Radic. Biol. Med. doi: 10.1016/j.freeradbiomed.2011.07.011 – volume: 99 start-page: 715 year: 2002 ident: 10.1016/j.canlet.2019.03.020_bib32 article-title: Reactive oxygen generated by Nox1 triggers the angiogenic switch publication-title: Proc. Natl. Acad. Sci. U. S. A. doi: 10.1073/pnas.022630199 – volume: 458 start-page: 780 year: 2009 ident: 10.1016/j.canlet.2019.03.020_bib118 article-title: Association of reactive oxygen species levels and radioresistance in cancer stem cells publication-title: Nature doi: 10.1038/nature07733 – volume: 138 start-page: 1058 year: 2016 ident: 10.1016/j.canlet.2019.03.020_bib87 article-title: HIF-1 at the crossroads of hypoxia, inflammation, and cancer publication-title: Int. J. Cancer doi: 10.1002/ijc.29519 – volume: 21 start-page: 379 year: 2000 ident: 10.1016/j.canlet.2019.03.020_bib9 article-title: Significance of multiple mutations in cancer publication-title: Carcinogenesis doi: 10.1093/carcin/21.3.379 – volume: 107 start-page: 8788 year: 2010 ident: 10.1016/j.canlet.2019.03.020_bib22 article-title: Mitochondrial metabolism and ROS generation are essential for Kras-mediated tumorigenicity publication-title: Proc. Natl. Acad. Sci. U. S. A. doi: 10.1073/pnas.1003428107 – volume: 6 start-page: 22836 year: 2015 ident: 10.1016/j.canlet.2019.03.020_bib104 article-title: Hypoxia induces triglycerides accumulation in prostate cancer cells and extracellular vesicles supporting growth and invasiveness following reoxygenation publication-title: Oncotarget doi: 10.18632/oncotarget.4479 – volume: 53 start-page: 1489 year: 2012 ident: 10.1016/j.canlet.2019.03.020_bib114 article-title: Nox4 involvement in TGF-beta and SMAD3-driven induction of the epithelial-to-mesenchymal transition and migration of breast epithelial cells publication-title: Free Radic. Biol. Med. doi: 10.1016/j.freeradbiomed.2012.06.016 – volume: 120 start-page: 513 year: 2005 ident: 10.1016/j.canlet.2019.03.020_bib128 article-title: Senescent cells, tumor suppression, and organismal aging: good citizens, bad neighbors publication-title: Cell doi: 10.1016/j.cell.2005.02.003 – volume: 36 start-page: 439 year: 2017 ident: 10.1016/j.canlet.2019.03.020_bib96 article-title: Hypoxic stress: obstacles and opportunities for innovative immunotherapy of cancer publication-title: Oncogene doi: 10.1038/onc.2016.225 – volume: 57 start-page: 99 year: 2012 ident: 10.1016/j.canlet.2019.03.020_bib18 article-title: Somatic mitochondrial DNA mutations in human cancers publication-title: Adv. Clin. Chem. doi: 10.1016/B978-0-12-394384-2.00004-8 – volume: 2 start-page: 23 year: 2003 ident: 10.1016/j.canlet.2019.03.020_bib80 article-title: Molecular responses to hypoxia in tumor cells publication-title: Mol. Canc. doi: 10.1186/1476-4598-2-23 – volume: 30 start-page: 2986 year: 2011 ident: 10.1016/j.canlet.2019.03.020_bib16 article-title: SirT3 suppresses hypoxia inducible factor 1α and tumor growth by inhibiting mitochondrial ROS production publication-title: Oncogene doi: 10.1038/onc.2011.37 – volume: 14 start-page: 709 year: 2014 ident: 10.1016/j.canlet.2019.03.020_bib5 article-title: Mitochondrial ROS in cancer: initiators, amplifiers or an Achilles' heel? publication-title: Nat. Rev. Canc. doi: 10.1038/nrc3803 – volume: 19 start-page: 385 year: 2007 ident: 10.1016/j.canlet.2019.03.020_bib76 article-title: The hypoxic tumour microenvironment, patient selection and hypoxia-modifying treatments publication-title: Clin. Oncol. doi: 10.1016/j.clon.2007.03.001 – volume: 25 start-page: 4706 year: 2006 ident: 10.1016/j.canlet.2019.03.020_bib17 article-title: Mitochondria and cancer: is there a morphological connection? publication-title: Oncogene doi: 10.1038/sj.onc.1209600 – volume: 19 start-page: 139 year: 2000 ident: 10.1016/j.canlet.2019.03.020_bib88 article-title: MAP kinases and hypoxia in the control of VEGF expression publication-title: Cancer Metastasis Rev. doi: 10.1023/A:1026506011458 – volume: 50 start-page: 645 year: 2018 ident: 10.1016/j.canlet.2019.03.020_bib55 article-title: The long tail of oncogenic drivers in prostate cancer publication-title: Nat. Genet. doi: 10.1038/s41588-018-0078-z – volume: 42 start-page: 378 year: 2015 ident: 10.1016/j.canlet.2019.03.020_bib99 article-title: Immune response regulation in the tumor microenvironment by hypoxia publication-title: Semin. Oncol. doi: 10.1053/j.seminoncol.2015.02.009 – volume: 7 start-page: 44879 year: 2016 ident: 10.1016/j.canlet.2019.03.020_bib126 article-title: Mitochondrial dysfunction and oxidative stress in aging and cancer publication-title: Oncotarget doi: 10.18632/oncotarget.9821 – volume: 62 start-page: 6470 year: 2002 ident: 10.1016/j.canlet.2019.03.020_bib28 article-title: Extensive somatic mitochondrial mutations in primary prostate cancer using laser capture microdissection publication-title: Cancer Res. – volume: 110 year: 2018 ident: 10.1016/j.canlet.2019.03.020_bib40 article-title: Targeting the myofibroblastic cancer-associated fibroblast phenotype through inhibition of NOX4 publication-title: J. Natl. Cancer Inst. doi: 10.1093/jnci/djx121 – volume: 8 start-page: 14437 year: 2017 ident: 10.1016/j.canlet.2019.03.020_bib42 article-title: Mutant Kras- and p16-regulated NOX4 activation overcomes metabolic checkpoints in development of pancreatic ductal adenocarcinoma publication-title: Nat. Commun. doi: 10.1038/ncomms14437 – volume: 116 start-page: 370 year: 2017 ident: 10.1016/j.canlet.2019.03.020_bib45 article-title: Regulation of anoikis resistance by NADPH oxidase 4 and epidermal growth factor receptor publication-title: Br. J. Canc. doi: 10.1038/bjc.2016.440 – volume: 27 start-page: 7150 year: 2008 ident: 10.1016/j.canlet.2019.03.020_bib108 article-title: Colorectal cancer cells with the BRAF(V600E) mutation are addicted to the ERK1/2 pathway for growth factor-independent survival and repression of BIM publication-title: Oncogene doi: 10.1038/onc.2008.335 – volume: 163 start-page: 1011 year: 2015 ident: 10.1016/j.canlet.2019.03.020_bib54 article-title: The molecular taxonomy of primary prostate cancer publication-title: Cell doi: 10.1016/j.cell.2015.10.025 – volume: 5 start-page: 415 year: 2000 ident: 10.1016/j.canlet.2019.03.020_bib20 article-title: Role of reactive oxygen species (ROS) in apoptosis induction publication-title: Apoptosis doi: 10.1023/A:1009616228304 – volume: 69 start-page: 2375 year: 2009 ident: 10.1016/j.canlet.2019.03.020_bib140 article-title: Mitochondrial dysfunction and reactive oxygen species imbalance promote breast cancer cell motility through a CXCL14-mediated mechanism publication-title: Cancer Res. doi: 10.1158/0008-5472.CAN-08-3359 – volume: 436 start-page: 123 year: 2005 ident: 10.1016/j.canlet.2019.03.020_bib132 article-title: Rac1b and reactive oxygen species mediate MMP-3-induced EMT and genomic instability publication-title: Nature doi: 10.1038/nature03688 – volume: 5 start-page: 7093 year: 2014 ident: 10.1016/j.canlet.2019.03.020_bib111 article-title: De-SUMOylation of FOXC2 by SENP3 promotes the epithelial-mesenchymal transition in gastric cancer cells publication-title: Oncotarget doi: 10.18632/oncotarget.2197 – year: 2017 ident: 10.1016/j.canlet.2019.03.020_bib31 article-title: NOX4-dependent neuronal autotoxicity and BBB breakdown explain the superior sensitivity of the brain to ischemic damage – volume: 100 start-page: 86 year: 2016 ident: 10.1016/j.canlet.2019.03.020_bib15 article-title: Mitochondrial ROS regulation of proliferating cells publication-title: Free Radic. Biol. Med. doi: 10.1016/j.freeradbiomed.2016.04.198 – volume: 436 start-page: 406 year: 2005 ident: 10.1016/j.canlet.2019.03.020_bib92 article-title: Regulation of MAP kinase-dependent apoptotic pathway: implication of reactive oxygen and nitrogen species publication-title: Arch. Biochem. Biophys. doi: 10.1016/j.abb.2005.02.021 – volume: 55 start-page: 27 year: 2016 ident: 10.1016/j.canlet.2019.03.020_bib36 article-title: ROS signaling by NADPH oxidase 5 modulates the proliferation and survival of prostate carcinoma cells publication-title: Mol. Carcinog. doi: 10.1002/mc.22255 – volume: 216 start-page: 435 year: 2016 ident: 10.1016/j.canlet.2019.03.020_bib47 article-title: The NADPH Oxidase Nox4 mediates tumour angiogenesis publication-title: Acta Physiol. doi: 10.1111/apha.12625 – volume: 410 start-page: 195 year: 2011 ident: 10.1016/j.canlet.2019.03.020_bib113 article-title: ROS enhances CXCR4-mediated functions through inactivation of PTEN in prostate cancer cells publication-title: Biochem. Biophys. Res. Commun. doi: 10.1016/j.bbrc.2011.05.074 – year: 2018 ident: 10.1016/j.canlet.2019.03.020_bib2 – volume: 9 start-page: 917 year: 2013 ident: 10.1016/j.canlet.2019.03.020_bib91 article-title: The many faces of C/EBPδ and their relevance for inflammation and cancer publication-title: Int. J. Biol. Sci. doi: 10.7150/ijbs.7224 – volume: 74 start-page: 6291 year: 2014 ident: 10.1016/j.canlet.2019.03.020_bib120 article-title: Distinct subpopulations of head and neck cancer cells with different levels of intracellular reactive oxygen species exhibit diverse stemness, proliferation, and chemosensitivity publication-title: Cancer Res. doi: 10.1158/0008-5472.CAN-14-0626 – volume: 24 start-page: 1481 year: 2003 ident: 10.1016/j.canlet.2019.03.020_bib27 article-title: Simultaneous generation of multiple mitochondrial DNA mutations in human prostate tumors suggests mitochondrial hyper-mutagenesis publication-title: Carcinogenesis doi: 10.1093/carcin/bgg102 – volume: 6 start-page: 482 year: 2015 ident: 10.1016/j.canlet.2019.03.020_bib100 article-title: Critical role of tumor microenvironment in shaping NK cell functions: implication of hypoxic stress publication-title: Front. Immunol. doi: 10.3389/fimmu.2015.00482 – volume: 166 start-page: 963 year: 2016 ident: 10.1016/j.canlet.2019.03.020_bib65 article-title: NRF2 promotes tumor maintenance by modulating mRNA translation in pancreatic cancer publication-title: Cell doi: 10.1016/j.cell.2016.06.056 – volume: 14 start-page: 427 year: 2008 ident: 10.1016/j.canlet.2019.03.020_bib145 article-title: AKT and oxidative stress team up to kill cancer cells publication-title: Cancer Cell doi: 10.1016/j.ccr.2008.11.006 – volume: 41 start-page: 52 year: 2015 ident: 10.1016/j.canlet.2019.03.020_bib72 article-title: Nrf2 sensitizes prostate cancer cells to radiation via decreasing basal ROS levels publication-title: Biofactors doi: 10.1002/biof.1200 – volume: 371 start-page: 177 year: 2014 ident: 10.1016/j.canlet.2019.03.020_bib58 article-title: The promise and perils of antioxidants for cancer patients publication-title: N. Engl. J. Med. doi: 10.1056/NEJMcibr1405701 – volume: 352 start-page: 245 year: 2017 ident: 10.1016/j.canlet.2019.03.020_bib66 article-title: Nrf2 mediates redox adaptation in NOX4-overexpressed non-small cell lung cancer cells publication-title: Exp. Cell Res. doi: 10.1016/j.yexcr.2017.02.014 – volume: 12 year: 2017 ident: 10.1016/j.canlet.2019.03.020_bib62 article-title: The NRF2 transcription factor plays a dual role in colorectal cancer: a systematic review publication-title: PLoS One doi: 10.1371/journal.pone.0177549 – volume: 4 year: 2013 ident: 10.1016/j.canlet.2019.03.020_bib74 article-title: Tumor hypoxia as a driving force in genetic instability publication-title: Genome Integr. doi: 10.1186/2041-9414-4-5 – volume: 99 start-page: 1441 year: 2007 ident: 10.1016/j.canlet.2019.03.020_bib75 article-title: Drug resistance and the solid tumor microenvironment publication-title: J. Natl. Cancer Inst. doi: 10.1093/jnci/djm135 – volume: 4 start-page: e537 year: 2013 ident: 10.1016/j.canlet.2019.03.020_bib119 article-title: Redox homeostasis: the linchpin in stem cell self-renewal and differentiation publication-title: Cell Death Dis. doi: 10.1038/cddis.2013.50 – volume: 5 start-page: 12070 year: 2014 ident: 10.1016/j.canlet.2019.03.020_bib135 article-title: Acidosis promotes invasiveness of breast cancer cells through ROS-AKT-NF-κB pathway publication-title: Oncotarget doi: 10.18632/oncotarget.2514 – volume: 282 start-page: 125 year: 2009 ident: 10.1016/j.canlet.2019.03.020_bib8 article-title: Oxidative stress in prostate cancer publication-title: Cancer Lett. doi: 10.1016/j.canlet.2008.12.011 – volume: 46 start-page: S7 year: 2014 ident: 10.1016/j.canlet.2019.03.020_bib12 article-title: Age and cancer risk: a potentially modifiable relationship publication-title: Am. J. Prev. Med. doi: 10.1016/j.amepre.2013.10.029 – volume: 28 start-page: 1248 year: 2009 ident: 10.1016/j.canlet.2019.03.020_bib93 article-title: Hypoxia-associated p38 mitogen-activated protein kinase-mediated androgen receptor activation and increased HIF-1alpha levels contribute to emergence of an aggressive phenotype in prostate cancer publication-title: Oncogene doi: 10.1038/onc.2008.476 – volume: 5 year: 2016 ident: 10.1016/j.canlet.2019.03.020_bib97 article-title: Hypoxia-induced soluble CD137 in malignant cells blocks CD137L-costimulation as an immune escape mechanism publication-title: OncoImmunology doi: 10.1080/2162402X.2015.1062967 – volume: 9 start-page: 3157 year: 2018 ident: 10.1016/j.canlet.2019.03.020_bib102 article-title: SENP3 maintains the stability and function of regulatory T cells via BACH2 deSUMOylation publication-title: Nat. Commun. doi: 10.1038/s41467-018-05676-6 – volume: 114 start-page: 1090 year: 2016 ident: 10.1016/j.canlet.2019.03.020_bib29 article-title: Mitochondrial dysfunction-mediated apoptosis resistance associates with defective heat shock protein response in African-American men with prostate cancer publication-title: Br. J. Canc. doi: 10.1038/bjc.2016.88 – volume: 483 start-page: 163 year: 2004 ident: 10.1016/j.canlet.2019.03.020_bib137 article-title: Activation of ERK1/2, JNK and PKB by hydrogen peroxide in human SH-SY5Y neuroblastoma cells: role of ERK1/2 in H2O2-induced cell death publication-title: Eur. J. Pharmacol. doi: 10.1016/j.ejphar.2003.10.032 – volume: 527 start-page: 186 year: 2015 ident: 10.1016/j.canlet.2019.03.020_bib59 article-title: Oxidative stress inhibits distant metastasis by human melanoma cells publication-title: Nature doi: 10.1038/nature15726 – volume: 22 start-page: 11 year: 2005 ident: 10.1016/j.canlet.2019.03.020_bib85 article-title: Oxidative stress in breast cancer publication-title: Med. Oncol. doi: 10.1385/MO:22:1:011 – volume: 143 start-page: 512 year: 2014 ident: 10.1016/j.canlet.2019.03.020_bib101 article-title: Hypoxia-inducible factors in regulation of immune responses in tumour microenvironment publication-title: Immunology doi: 10.1111/imm.12380 – volume: 31 start-page: 1608 year: 2017 ident: 10.1016/j.canlet.2019.03.020_bib61 article-title: Endostatin inhibits androgen-independent prostate cancer growth by suppressing nuclear receptor-mediated oxidative stress publication-title: FASEB J. doi: 10.1096/fj.201601178R – volume: 29 start-page: 713 year: 2008 ident: 10.1016/j.canlet.2019.03.020_bib131 article-title: Reactive oxygen species stabilize hypoxia-inducible factor-1 alpha protein and stimulate transcriptional activity via AMP-activated protein kinase in DU145 human prostate cancer cells publication-title: Carcinogenesis doi: 10.1093/carcin/bgn032 – volume: 2 year: 2015 ident: 10.1016/j.canlet.2019.03.020_bib23 article-title: Paving the way for therapeutic prevention of tumor metastasis with agents targeting mitochondrial superoxide publication-title: Mol Cell Oncol – volume: 5 start-page: 4392 year: 2014 ident: 10.1016/j.canlet.2019.03.020_bib44 article-title: NOX4 promotes non-small cell lung cancer cell proliferation and metastasis through positive feedback regulation of PI3K/Akt signaling publication-title: Oncotarget doi: 10.18632/oncotarget.2025 – volume: 404 start-page: 34 year: 2011 ident: 10.1016/j.canlet.2019.03.020_bib142 article-title: Snail-mediated regulation of reactive oxygen species in ARCaP human prostate cancer cells publication-title: Biochem. Biophys. Res. Commun. doi: 10.1016/j.bbrc.2010.11.044 – volume: 34 start-page: 239 year: 2016 ident: 10.1016/j.canlet.2019.03.020_bib78 article-title: Tumor hypoxia and reoxygenation: the yin and yang for radiotherapy publication-title: Radiation Oncology Journal doi: 10.3857/roj.2016.02012 – volume: 2 start-page: 17 year: 2014 ident: 10.1016/j.canlet.2019.03.020_bib14 article-title: Mitochondrial reactive oxygen species and cancer publication-title: Cancer Metabol. doi: 10.1186/2049-3002-2-17 – volume: 23 start-page: 316 year: 2013 ident: 10.1016/j.canlet.2019.03.020_bib123 article-title: Loss of FBP1 by Snail-mediated repression provides metabolic advantages in basal-like breast cancer publication-title: Cancer Cell doi: 10.1016/j.ccr.2013.01.022 – volume: 14 start-page: 458 year: 2008 ident: 10.1016/j.canlet.2019.03.020_bib144 article-title: Akt determines replicative senescence and oxidative or oncogenic premature senescence and sensitizes cells to oxidative apoptosis publication-title: Cancer Cell doi: 10.1016/j.ccr.2008.11.003 – volume: 47 start-page: 57 year: 2017 ident: 10.1016/j.canlet.2019.03.020_bib13 article-title: Mitochondrial ROS control of cancer publication-title: Semin. Canc. Biol. doi: 10.1016/j.semcancer.2017.04.005 – volume: 44 start-page: 331 year: 2015 ident: 10.1016/j.canlet.2019.03.020_bib109 article-title: Peroxiredoxin 1 promotes pancreatic cancer cell invasion by modulating p38 MAPK activity publication-title: Pancreas doi: 10.1097/MPA.0000000000000270 – volume: 8 start-page: 3781 year: 2018 ident: 10.1016/j.canlet.2019.03.020_bib116 article-title: Nox4 is a target for tuberin deficiency syndrome publication-title: Sci. Rep. doi: 10.1038/s41598-018-21838-4 – volume: 87 start-page: 245 year: 2007 ident: 10.1016/j.canlet.2019.03.020_bib30 article-title: The NOX family of ROS-generating NADPH oxidases: physiology and pathophysiology publication-title: Physiol. Rev. doi: 10.1152/physrev.00044.2005 – volume: 8 start-page: 180 year: 2008 ident: 10.1016/j.canlet.2019.03.020_bib77 article-title: Hypoxia and metabolism. Hypoxia, DNA repair and genetic instability publication-title: Nat. Rev. Canc. doi: 10.1038/nrc2344 – volume: 16 start-page: 4932 year: 2010 ident: 10.1016/j.canlet.2019.03.020_bib136 article-title: HBx-induced reactive oxygen species activates hepatocellular carcinogenesis via dysregulation of PTEN/Akt pathway publication-title: World J. Gastroenterol. doi: 10.3748/wjg.v16.i39.4932 – volume: 37 start-page: 169 year: 2001 ident: 10.1016/j.canlet.2019.03.020_bib25 article-title: Accumulation of mitochondrial DNA deletions in the malignant prostate of patients of different ages publication-title: Exp. Gerontol. doi: 10.1016/S0531-5565(01)00153-X – volume: 8 start-page: 67506 year: 2017 ident: 10.1016/j.canlet.2019.03.020_bib69 article-title: ROS-independent Nrf2 activation in prostate cancer publication-title: Oncotarget doi: 10.18632/oncotarget.18724 – volume: 2016 year: 2016 ident: 10.1016/j.canlet.2019.03.020_bib98 article-title: The interplay of reactive oxygen species, hypoxia, inflammation, and sirtuins in cancer initiation and progression publication-title: Oxid Med Cell Longev doi: 10.1155/2016/3907147 – volume: 23 start-page: 227 year: 2000 ident: 10.1016/j.canlet.2019.03.020_bib4 article-title: The nature and mechanism of superoxide production by the electron transport chain: its relevance to aging publication-title: J Am Aging Assoc – volume: 2 start-page: 242 year: 2013 ident: 10.1016/j.canlet.2019.03.020_bib124 article-title: Cancer stem cells in prostate cancer publication-title: Transl. Androl. Urol. – volume: 25 start-page: 503 year: 2011 ident: 10.1016/j.canlet.2019.03.020_bib41 article-title: ROS signaling by NOX4 drives fibroblast-to-myofibroblast differentiation in the diseased prostatic stroma publication-title: Mol. Endocrinol. doi: 10.1210/me.2010-0340 – volume: 27 start-page: 156 year: 2015 ident: 10.1016/j.canlet.2019.03.020_bib11 article-title: Reactive oxygen species in cancer: a dance with the devil publication-title: Cancer Cell doi: 10.1016/j.ccell.2015.01.007 – volume: 109 start-page: 983 year: 2013 ident: 10.1016/j.canlet.2019.03.020_bib110 article-title: Peroxiredoxin-3 is overexpressed in prostate cancer and promotes cancer cell survival by protecting cells from oxidative stress publication-title: Br. J. Canc. doi: 10.1038/bjc.2013.396 – volume: 163 start-page: 2513 year: 2003 ident: 10.1016/j.canlet.2019.03.020_bib34 article-title: Androgenic regulation of oxidative stress in the rat prostate: involvement of NAD(P)H oxidases and antioxidant defense machinery during prostatic involution and regrowth publication-title: Am. J. Pathol. doi: 10.1016/S0002-9440(10)63606-1 – volume: 25 start-page: 183 year: 2005 ident: 10.1016/j.canlet.2019.03.020_bib57 article-title: Identification of metastasis-associated genes in prostate cancer by genetic profiling of human prostate cancer cell lines publication-title: Anticancer Res. – volume: 59 start-page: 10 year: 2006 ident: 10.1016/j.canlet.2019.03.020_bib24 article-title: Altered metabolism and mitochondrial genome in prostate cancer publication-title: J. Clin. Pathol. doi: 10.1136/jcp.2005.027664 – volume: 275 start-page: 7087 year: 2000 ident: 10.1016/j.canlet.2019.03.020_bib19 article-title: Lack of oxidative phosphorylation and low mitochondrial membrane potential decrease susceptibility to apoptosis and do not modulate the protective effect of Bcl-x(L) in osteosarcoma cells publication-title: J. Biol. Chem. doi: 10.1074/jbc.275.10.7087 – volume: 22 start-page: 66 year: 2012 ident: 10.1016/j.canlet.2019.03.020_bib64 article-title: Nrf2 redirects glucose and glutamine into anabolic pathways in metabolic reprogramming publication-title: Cancer Cell doi: 10.1016/j.ccr.2012.05.016 – volume: 475 start-page: 106 year: 2011 ident: 10.1016/j.canlet.2019.03.020_bib67 article-title: Oncogene-induced Nrf2 transcription promotes ROS detoxification and tumorigenesis publication-title: Nature doi: 10.1038/nature10189 – year: 2018 ident: 10.1016/j.canlet.2019.03.020_bib117 article-title: ROS release by PPARβ/δ-null fibroblasts reduces tumor load through epithelial antioxidant response publication-title: Oncogene doi: 10.1038/s41388-017-0109-8 – volume: 2016 year: 2016 ident: 10.1016/j.canlet.2019.03.020_bib63 article-title: Redox modulating NRF2: a potential mediator of cancer stem cell resistance publication-title: Oxid Med Cell Longev doi: 10.1155/2016/2428153 – volume: 36 start-page: 3002 year: 2017 ident: 10.1016/j.canlet.2019.03.020_bib115 article-title: The NADPH oxidase NOX4 represses epithelial to amoeboid transition and efficient tumour dissemination publication-title: Oncogene doi: 10.1038/onc.2016.454 – volume: 22 start-page: 298 year: 2016 ident: 10.1016/j.canlet.2019.03.020_bib53 article-title: Divergent clonal evolution of castration-resistant neuroendocrine prostate cancer publication-title: Nat. Med. doi: 10.1038/nm.4045 – volume: 12 start-page: 41 year: 1995 ident: 10.1016/j.canlet.2019.03.020_bib84 article-title: Release of hydrogen peroxide in response to hypoxia-reoxygenation: role of an NAD(P)H oxidase-like enzyme in endothelial cell plasma membrane publication-title: Am. J. Respir. Cell Mol. Biol. doi: 10.1165/ajrcmb.12.1.7529030 – volume: 20 start-page: 419 year: 2015 ident: 10.1016/j.canlet.2019.03.020_bib103 article-title: Hypoxia-induced signaling promotes prostate cancer progression: exosomes role as messenger of hypoxic response in tumor microenvironment publication-title: Crit. Rev. Oncog. doi: 10.1615/CritRevOncog.v20.i5-6.130 – volume: 44 start-page: 685 year: 2012 ident: 10.1016/j.canlet.2019.03.020_bib56 article-title: Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer publication-title: Nat. Genet. doi: 10.1038/ng.2279 – volume: 68 start-page: 1777 year: 2008 ident: 10.1016/j.canlet.2019.03.020_bib6 article-title: Oxidative stress is inherent in prostate cancer cells and is required for aggressive phenotype publication-title: Cancer Res. doi: 10.1158/0008-5472.CAN-07-5259 – volume: 18 start-page: 11 year: 2010 ident: 10.1016/j.canlet.2019.03.020_bib49 article-title: Integrative genomic profiling of human prostate cancer publication-title: Cancer Cell doi: 10.1016/j.ccr.2010.05.026 – volume: 14 start-page: 252 year: 2014 ident: 10.1016/j.canlet.2019.03.020_bib94 article-title: Effect of hypoxia on the expression of αB-crystallin in head and neck squamous cell carcinoma publication-title: BMC Canc. doi: 10.1186/1471-2407-14-252 – volume: 47 start-page: 53 year: 2010 ident: 10.1016/j.canlet.2019.03.020_bib83 article-title: Mitochondrial proton and electron leaks publication-title: Essays Biochem. doi: 10.1042/bse0470053 – volume: 19 start-page: S539 issue: Suppl 3 year: 2012 ident: 10.1016/j.canlet.2019.03.020_bib121 article-title: Increased CD13 expression reduces reactive oxygen species, promoting survival of liver cancer stem cells via an epithelial-mesenchymal transition-like phenomenon publication-title: Ann. Surg. Oncol. doi: 10.1245/s10434-011-2040-5 – volume: 26 start-page: 388 year: 2015 ident: 10.1016/j.canlet.2019.03.020_bib43 article-title: Inhibition of NADPH oxidase protects against metastasis of human lung cancer by decreasing microRNA-21 publication-title: Anti Canccer Drugs doi: 10.1097/CAD.0000000000000198 – volume: 13 start-page: 815 year: 2017 ident: 10.1016/j.canlet.2019.03.020_bib107 article-title: FOXO signaling pathways as therapeutic targets in cancer publication-title: Int. J. Biol. Sci. doi: 10.7150/ijbs.20052 – volume: 36 start-page: 521 year: 2016 ident: 10.1016/j.canlet.2019.03.020_bib105 article-title: Hypoxia inducible factor-1α-dependent epithelial to mesenchymal transition under hypoxic conditions in prostate cancer cells publication-title: Oncol. Rep. doi: 10.3892/or.2016.4766 – volume: 153 start-page: 666 year: 2013 ident: 10.1016/j.canlet.2019.03.020_bib51 article-title: Punctuated evolution of prostate cancer genomes publication-title: Cell doi: 10.1016/j.cell.2013.03.021 – volume: 2 start-page: 85 year: 2014 ident: 10.1016/j.canlet.2019.03.020_bib79 article-title: Population dynamics inside cancer biomass driven by repeated hypoxia-reoxygenation cycles publication-title: Quantitative Biology doi: 10.1007/s40484-014-0032-8 – volume: 7 start-page: 39692 year: 2017 ident: 10.1016/j.canlet.2019.03.020_bib95 article-title: TRIM14 is a putative tumor suppressor and regulator of innate immune response in non-small cell lung cancer publication-title: Sci. Rep. doi: 10.1038/srep39692 – volume: 13 start-page: 182 year: 2017 ident: 10.1016/j.canlet.2019.03.020_bib35 article-title: Decoding NADPH oxidase 4 expression in human tumors publication-title: Redox Biol doi: 10.1016/j.redox.2017.05.016 – volume: 9 year: 2014 ident: 10.1016/j.canlet.2019.03.020_bib71 article-title: Nrf1 and Nrf2 transcription factors regulate androgen receptor transactivation in prostate cancer cells publication-title: PLoS One doi: 10.1371/journal.pone.0087204 – volume: 2016 year: 2016 ident: 10.1016/j.canlet.2019.03.020_bib73 article-title: TGF-β and hypoxia/reoxygenation promote radioresistance of A549 lung cancer cells through activation of Nrf2 and EGFR publication-title: Oxid Med Cell Longev doi: 10.1155/2016/6823471 |
SSID | ssj0005475 |
Score | 2.640662 |
SecondaryResourceType | review_article |
Snippet | Elevated levels of Reactive Oxygen Species (ROS), increased antioxidant ability and the maintenance of redox homeostasis can cumulatively contribute to tumor... |
SourceID | proquest pubmed crossref elsevier |
SourceType | Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 132 |
SubjectTerms | Androgens Antioxidants Apoptosis Breast cancer Cancer Cancer therapies Cell Hypoxia - physiology Deoxyribonucleic acid DNA DNA methylation Genotype & phenotype Homeostasis Humans Hypoxia Hypoxia Re-Oxygenation Metabolism Metabolites Metastases Metastasis Mitochondria Mitochondrial DNA Mutation NADPH Oxidase 4 - metabolism Neoplasms - pathology NF-E2-Related Factor 2 - metabolism Ovarian cancer Oxidation-Reduction Oxidative stress Prostate cancer Reactive oxygen species Reactive Oxygen Species - metabolism ROS Signal Transduction Solid tumors Transcription factors Tumor Microenvironment - physiology Tumorigenesis Tumors |
Title | Reactive oxygen species and cancer: A complex interaction |
URI | https://www.clinicalkey.com/#!/content/1-s2.0-S0304383519301764 https://dx.doi.org/10.1016/j.canlet.2019.03.020 https://www.ncbi.nlm.nih.gov/pubmed/30905813 https://www.proquest.com/docview/2203685856 https://www.proquest.com/docview/2197323297 |
Volume | 452 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3fS9xAEB5EQXwpamt7esoW-ppekv3t23Eop6IPVsG3JcluwFJyx3mCvvi3O7NJDgstlj4mmYHNt7Ozs8zMtwDfaq-ULEOeBFvyRHBvEyskPsoyCz7T3ERKocsrNb0V53fybg0mfS8MlVV2vr_16dFbd29GHZqj-f396Acl9fB8RSEImpUiTlAhNFn595c3ZR4iku2ScELSfftcrPHC0SM6VODVUp3Srd9_3p7-Fn7Gbeh0Gz508SMbt0PcgbXQ7MLmZZch_wj2OhTRhbHZ0zMaB6NWSjwNs6LxrKIpXhyzMYuV5OGJEVvEou1t-AS3pyc3k2nSXY-QVELwZZKpPFOm1sYGyiYaXxurUy88xlxeycrXQZXCSMMrwXMrtEk9z3zqNed1jdv0Hqw3syZ8AZb5IArtecFTI0prC5l6G2rErhRVUfMB8B4VV3Xc4XSFxS_XF4n9dC2WjrB0KXeI5QCSlda85c54R172gLu-LxQ9mUPn_o6eXun9Zjv_oDns59V1a_fB5RFNPEapAXxdfcZVR6mUogmzR5TJiOUIUdUD-Nzaw-oXeWpTaTK-_9_DOoAteqKKtNwMYX25eAyHGPssy6No3EewMT67mF69Ah44AEA |
linkProvider | Elsevier |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV3NT9RAFH8hmKgXo6KyCjomeKzbdj46Q8KBKGQRloNCwm1sO9MEQrpkWSJc_Kf8B3lvOt1IAsGYcGw7L5n-5s1v3uR9Aaw1TilZ-TzxpuKJ4M4kRkh8lFXmXVZwHUoKjffV6FB8O5JHC_Cnz4WhsMrI_R2nB7aOb4YRzeHZ8fHwBzn18H5FJgiqlRIxsnLXX_3Ce9v5xs5XXORPeb69dfBllMTWAkktBJ8lmcozpZtCG0-eOO0abYrUCYf2ilOydo1XldBS81rw3IhCp45nLnUF502jqVUE8v4jgXRBbRM-__4rrkSE6r40u4Sm1-frhaAyhAuXgyLKutqq1Gb89vPwLns3nHvbz-FZNFjZZofJC1jw7Ut4PI4u-SUw330ZOJNNLq9QGxnlbuL1m5WtYzXp1HSdbbIQuu4vGZWnmHbJFK_g8EFAew2L7aT1y8Ay50VZOF7yVIvKmFKmzvgGsatEXTZ8ALxHxdaxWDn1zDi1fVTaie2wtISlTblFLAeQzKXOumId94yXPeC2T0RF6rR4mtwjV8zlbijrP0iu9OtqI1mc2zygifc2NYCP88-4zcl3U7Z-coFjMiqrhKgWA3jT6cP8F3lqUqkz_va_p_UBnowOxnt2b2d_9x08pS8UDpfrFVicTS_8Khpes-p9UHQGPx96Z10DUmQ5sg |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Reactive+oxygen+species+and+cancer%3A+A+complex+interaction&rft.jtitle=Cancer+letters&rft.au=Sankaralingam+Saikolappan&rft.au=Kumar%2C+Binod&rft.au=Shishodia%2C+Gauri&rft.au=Koul%2C+Sweaty&rft.date=2019-06-28&rft.pub=Elsevier+Limited&rft.issn=0304-3835&rft.eissn=1872-7980&rft.volume=452&rft.spage=132&rft_id=info:doi/10.1016%2Fj.canlet.2019.03.020&rft.externalDBID=NO_FULL_TEXT |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0304-3835&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0304-3835&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0304-3835&client=summon |