Elevated lipogenesis in epithelial stem-like cell confers survival advantage in ductal carcinoma in situ of breast cancer
Upregulation of lipogenesis is a hallmark of cancer and blocking the lipogenic pathway is known to cause tumor cell death by apoptosis. However, the exact role of lipogenesis in tumor initiation is as yet poorly understood. We examined the expression profile of key lipogenic genes in clinical sample...
Saved in:
Published in | Oncogene Vol. 32; no. 42; pp. 5111 - 5122 |
---|---|
Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
17.10.2013
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Upregulation of lipogenesis is a hallmark of cancer and blocking the lipogenic pathway is known to cause tumor cell death by apoptosis. However, the exact role of lipogenesis in tumor initiation is as yet poorly understood. We examined the expression profile of key lipogenic genes in clinical samples of ductal carcinoma
in situ
(DCIS) of breast cancer and found that these genes were significantly upregulated in DCIS. We also isolated cancer stem-like cells (CSCs) from DCIS.com cell line using cell surface markers (CS24
−
CD44
+
ESA
+
) and found that this cell population has significantly higher tumor-initiating ability to generate DCIS compared with the non-stem-like population. Furthermore, the CSCs showed significantly higher level of expression of all lipogenic genes than the counterpart population from non-tumorigenic breast cancer cell line, MCF10A. Importantly, ectopic expression of SREBP1, the master regulator of lipogenic genes, in MCF10A significantly enhanced lipogenesis in stem-like cells and promoted cell growth as well as mammosphere formation. Moreover, SREBP1 expression significantly increased the ability of cell survival of CSCs from MCF10AT, another cell line that is capable of generating DCIS, in mouse and in cell culture. These results indicate that upregulation of lipogenesis is a pre-requisite for DCIS formation by endowing the ability of cell survival. We have also shown that resveratrol was capable of blocking the lipogenic gene expression in CSCs and significantly suppressed their ability to generate DCIS in animals, which provides us with a strong rationale to use this agent for chemoprevention against DCIS. |
---|---|
AbstractList | Upregulation of lipogenesis is a hallmark of cancer and blocking the lipogenic pathway is known to cause tumor cell death by apoptosis. However, the exact role of lipogenesis in tumor initiation is as yet poorly understood. We examined the expression profile of key lipogenic genes in clinical samples of ductal carcinoma
in situ
(DCIS) of breast cancer and found that these genes were significantly upregulated in DCIS. We also isolated cancer stem-like cells (CSCs) from DCIS.com cell line using cell surface markers (CS24
−
CD44
+
ESA
+
) and found that this cell population has significantly higher tumor-initiating ability to generate DCIS compared with the non-stem-like population. Furthermore, the CSCs showed significantly higher level of expression of all lipogenic genes than the counterpart population from non-tumorigenic breast cancer cell line, MCF10A. Importantly, ectopic expression of SREBP1, the master regulator of lipogenic genes, in MCF10A significantly enhanced lipogenesis in stem-like cells and promoted cell growth as well as mammosphere formation. Moreover, SREBP1 expression significantly increased the ability of cell survival of CSCs from MCF10AT, another cell line that is capable of generating DCIS, in mouse and in cell culture. These results indicate that upregulation of lipogenesis is a pre-requisite for DCIS formation by endowing the ability of cell survival. We have also shown that resveratrol was capable of blocking the lipogenic gene expression in CSCs and significantly suppressed their ability to generate DCIS in animals, which provides us with a strong rationale to use this agent for chemoprevention against DCIS. Upregulation of lipogenesis is a hallmark of cancer and blocking the lipogenic pathway is known to cause tumor cell death by apoptosis. However, the exact role of lipogenesis in tumor initiation is as yet poorly understood. We examined the expression profile of key lipogenic genes in clinical samples of ductal carcinoma in situ (DCIS) of breast cancer and found that these genes were significantly upregulated in DCIS. We also isolated cancer stem-like cells (CSCs) from DCIS.com cell line using cell surface markers (CS24(-)CD44(+)ESA(+)) and found that this cell population has significantly higher tumor-initiating ability to generate DCIS compared with the non-stem-like population. Furthermore, the CSCs showed significantly higher level of expression of all lipogenic genes than the counterpart population from non-tumorigenic breast cancer cell line, MCF10A. Importantly, ectopic expression of SREBP1, the master regulator of lipogenic genes, in MCF10A significantly enhanced lipogenesis in stem-like cells and promoted cell growth as well as mammosphere formation. Moreover, SREBP1 expression significantly increased the ability of cell survival of CSCs from MCF10AT, another cell line that is capable of generating DCIS, in mouse and in cell culture. These results indicate that upregulation of lipogenesis is a pre-requisite for DCIS formation by endowing the ability of cell survival. We have also shown that resveratrol was capable of blocking the lipogenic gene expression in CSCs and significantly suppressed their ability to generate DCIS in animals, which provides us with a strong rationale to use this agent for chemoprevention against DCIS. Upregulation of lipogenesis is a hallmark of cancer and blocking the lipogenic pathway is known to cause tumor cell death by apoptosis. However, the exact role of lipogenesis in tumor initiation is as yet poorly understood. We examined the expression profile of key lipogenic genes in clinical samples of ductal carcinoma in situ (DCIS) of breast cancer and found that these genes were significantly upregulated in DCIS. We also isolated cancer stem-like cells (CSCs) from DCIS.com cell line using cell surface markers (CS24(-)CD44(+)ESA(+)) and found that this cell population has significantly higher tumor-initiating ability to generate DCIS compared with the non-stem-like population. Furthermore, the CSCs showed significantly higher level of expression of all lipogenic genes than the counterpart population from non-tumorigenic breast cancer cell line, MCF10A. Importantly, ectopic expression of SREBP1, the master regulator of lipogenic genes, in MCF10A significantly enhanced lipogenesis in stem-like cells and promoted cell growth as well as mammosphere formation. Moreover, SREBP1 expression significantly increased the ability of cell survival of CSCs from MCF10AT, another cell line that is capable of generating DCIS, in mouse and in cell culture. These results indicate that upregulation of lipogenesis is a pre-requisite for DCIS formation by endowing the ability of cell survival. We have also shown that resveratrol was capable of blocking the lipogenic gene expression in CSCs and significantly suppressed their ability to generate DCIS in animals, which provides us with a strong rationale to use this agent for chemoprevention against DCIS. [PUBLICATION ABSTRACT] Upregulation of lipogenesis is a hallmark of cancer and blocking the lipogenic pathway is known to cause tumor cell death by apoptosis. However, the exact role of lipogenesis in tumor initiation is as yet poorly understood. We examined the expression profile of key lipogenic genes in clinical samples of ductal carcinoma in situ (DCIS) of breast cancer and found that these genes were significantly upregulated in DCIS. We also isolated cancer stem-like cells (CSCs) from DCIS.com cell line using cell surface markers ([CS24.sup.-] [CD44.sup.+] [ESA.sup.+]) and found that this cell population has significantly higher tumor-initiating ability to generate DCIS compared with the non-stem-like population. Furthermore, the CSCs showed significantly higher level of expression of all lipogenic genes than the counterpart population from non-tumorigenic breast cancer cell line, MCF10A. Importantly, ectopic expression of SREBP1, the master regulator of lipogenic genes, in MCF10A significantly enhanced lipogenesis in stem-like cells and promoted cell growth as well as mammosphere formation. Moreover, SREBP1 expression significantly increased the ability of cell survival of CSCs from MCF10AT, another cell line that is capable of generating DCIS, in mouse and in cell culture. These results indicate that upregulation of lipogenesis is a pre-requisite for DCIS formation by endowing the ability of cell survival. We have also shown that resveratrol was capable of blocking the lipogenic gene expression in CSCs and significantly suppressed their ability to generate DCIS in animals, which provides us with a strong rationale to use this agent for chemoprevention against DCIS. Oncogene (2013) 32, 5111-5122; doi:10.1038/onc.2012.519; published online 3 December 2012 Keywords: lipogenesis; ductal carcinoma in situ; breast cancer; stem-like cells; apoptosis; resveratrol Upregulation of lipogenesis is a hallmark of cancer and blocking the lipogenic pathway is known to cause tumor cell death by apoptosis. However, the exact role of lipogenesis in tumor initiation is as yet poorly understood. We examined the expression profile of key lipogenic genes in clinical samples of ductal carcinoma in situ (DCIS) of breast cancer and found that these genes were significantly upregulated in DCIS. We also isolated cancer stem-like cells (CSCs) from DCIS.com cell line using cell surface markers (CS24−CD44+ESA+) and found that this cell population has significantly higher tumor-initiating ability to generate DCIS compared with the non-stem-like population. Furthermore, the CSCs showed significantly higher level of expression of all lipogenic genes than the counterpart population from non-tumorigenic breast cancer cell line, MCF10A. Importantly, ectopic expression of SREBP1, the master regulator of lipogenic genes, in MCF10A significantly enhanced lipogenesis in stem-like cells and promoted cell growth as well as mammosphere formation. Moreover, SREBP1 expression significantly increased the ability of cell survival of CSCs from MCF10AT, another cell line that is capable of generating DCIS, in mouse and in cell culture. These results indicate that upregulation of lipogenesis is a pre-requisite for DCIS formation by endowing the ability of cell survival. We have also shown that resveratrol was capable of blocking the lipogenic gene expression in CSCs and significantly suppressed their ability to generate DCIS in animals, which provides us with a strong rationale to use this agent for chemoprevention against DCIS. Upregulation of lipogenesis is a hallmark of cancer and blocking the lipogenic pathway is known to cause tumor cell death by apoptosis. However, the exact role of lipogenesis in tumor initiation is as yet poorly understood. We examined the expression profile of key lipogenic genes in clinical samples of ductal carcinoma in situ (DCIS) of breast cancer and found that these genes were significantly upregulated in DCIS. We also isolated cancer stem-like cells (CSCs) from DCIS.com cell line using cell surface markers (CS24 super(-)CD44 super(+)ESA super(+)) and found that this cell population has significantly higher tumor-initiating ability to generate DCIS compared with the non-stem-like population. Furthermore, the CSCs showed significantly higher level of expression of all lipogenic genes than the counterpart population from non-tumorigenic breast cancer cell line, MCF10A. Importantly, ectopic expression of SREBP1, the master regulator of lipogenic genes, in MCF10A significantly enhanced lipogenesis in stem-like cells and promoted cell growth as well as mammosphere formation. Moreover, SREBP1 expression significantly increased the ability of cell survival of CSCs from MCF10AT, another cell line that is capable of generating DCIS, in mouse and in cell culture. These results indicate that upregulation of lipogenesis is a pre-requisite for DCIS formation by endowing the ability of cell survival. We have also shown that resveratrol was capable of blocking the lipogenic gene expression in CSCs and significantly suppressed their ability to generate DCIS in animals, which provides us with a strong rationale to use this agent for chemoprevention against DCIS. Upregulation of lipogenesis is a hallmark of cancer and blocking the lipogenic pathway is known to cause tumor cell death by apoptosis. However, the exact role of lipogenesis in tumor initiation is as yet poorly understood. We examined the expression profile of key lipogenic genes in clinical samples of ductal carcinoma in situ (DCIS) of breast cancer and found that these genes were significantly upregulated in DCIS. We also isolated cancer stem-like cells (CSCs) from DCIS.com cell line using cell surface markers ([CS24.sup.-] [CD44.sup.+] [ESA.sup.+]) and found that this cell population has significantly higher tumor-initiating ability to generate DCIS compared with the non-stem-like population. Furthermore, the CSCs showed significantly higher level of expression of all lipogenic genes than the counterpart population from non-tumorigenic breast cancer cell line, MCF10A. Importantly, ectopic expression of SREBP1, the master regulator of lipogenic genes, in MCF10A significantly enhanced lipogenesis in stem-like cells and promoted cell growth as well as mammosphere formation. Moreover, SREBP1 expression significantly increased the ability of cell survival of CSCs from MCF10AT, another cell line that is capable of generating DCIS, in mouse and in cell culture. These results indicate that upregulation of lipogenesis is a pre-requisite for DCIS formation by endowing the ability of cell survival. We have also shown that resveratrol was capable of blocking the lipogenic gene expression in CSCs and significantly suppressed their ability to generate DCIS in animals, which provides us with a strong rationale to use this agent for chemoprevention against DCIS. |
Audience | Academic |
Author | Pai, S K Xing, F Pandey, P R Iiizumi-Gairani, M Mo, Y-Y Watabe, K Sharma, S Fukuda, K Hirota, S Watabe, M |
Author_xml | – sequence: 1 givenname: P R surname: Pandey fullname: Pandey, P R organization: Department of Medical Microbiology, Immunology and Cell Biology, Southern Illinois University School of Medicine – sequence: 2 givenname: F surname: Xing fullname: Xing, F organization: Department of Medical Microbiology, Immunology and Cell Biology, Southern Illinois University School of Medicine, Cancer Institute, University of Mississippi Medical Center – sequence: 3 givenname: S surname: Sharma fullname: Sharma, S organization: Department of Medical Microbiology, Immunology and Cell Biology, Southern Illinois University School of Medicine – sequence: 4 givenname: M surname: Watabe fullname: Watabe, M organization: Department of Medical Microbiology, Immunology and Cell Biology, Southern Illinois University School of Medicine – sequence: 5 givenname: S K surname: Pai fullname: Pai, S K organization: Department of Medical Microbiology, Immunology and Cell Biology, Southern Illinois University School of Medicine – sequence: 6 givenname: M surname: Iiizumi-Gairani fullname: Iiizumi-Gairani, M organization: Department of Medical Microbiology, Immunology and Cell Biology, Southern Illinois University School of Medicine – sequence: 7 givenname: K surname: Fukuda fullname: Fukuda, K organization: Department of Medical Microbiology, Immunology and Cell Biology, Southern Illinois University School of Medicine – sequence: 8 givenname: S surname: Hirota fullname: Hirota, S organization: Department of Gastroenterology and Hepatology, School of Medicine, Iwate Medical University – sequence: 9 givenname: Y-Y surname: Mo fullname: Mo, Y-Y organization: Cancer Institute, University of Mississippi Medical Center – sequence: 10 givenname: K surname: Watabe fullname: Watabe, K email: kwatabe@umc.edu organization: Department of Medical Microbiology, Immunology and Cell Biology, Southern Illinois University School of Medicine, Cancer Institute, University of Mississippi Medical Center |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/23208501$$D View this record in MEDLINE/PubMed |
BookMark | eNp9kslr3DAUxkVJaZb21nMx9NJDPdVi2dYxhHSBQC_tWWikp6lSW5pK8kD--zwz6UooOgi-93sr3zk5iSkCIS8Z3TAqxncp2g2njG8kU0_IGeuGvpVSdSfkjCpJW8UFPyXnpdxSSgdF-TNyihIdJWVn5O56goOp4Jop7NMOIpRQmhAb2If6DaZgpqZUmNspfIfGwjQ1NkUPuTRlyYdwwLhxBxOr2cGa5xZbUbMm2xDTbFathLo0yTfbDKZUjEUL-Tl56s1U4MXDf0G-vr_-cvWxvfn84dPV5U1rJRe1VVZJ68wwGD7KQXbCKyHMVnrr-5H1tqd-65zrnR9wKWuZH4U1vRVCUKncIC7Im2PdfU4_FihVz6Gsi5gIaSmadd3I8WqSIfr6H_Q2LTnidJr3HZNcUvVfCmtxvD-V_W9qZybQIfpUs7Fra30pOjVwPvIRqc0jFD4Hc8BDgw-o_5Xw9phgcyolg9f7HGaT7zSjevWDRj_o1Q8a_YD4q4dZl-0M7hf80wAItEegYCjuIP-xzGMF7wEzz7_6 |
CODEN | ONCNES |
CitedBy_id | crossref_primary_10_3389_fonc_2022_899987 crossref_primary_10_1080_14728222_2017_1381087 crossref_primary_10_1016_j_cytogfr_2023_05_002 crossref_primary_10_1007_s12015_022_10348_6 crossref_primary_10_18632_oncotarget_2059 crossref_primary_10_1021_acsnano_3c07828 crossref_primary_10_2174_1568009619666210316112333 crossref_primary_10_1007_s41403_023_00417_8 crossref_primary_10_3389_fphar_2019_00709 crossref_primary_10_3390_cells9010007 crossref_primary_10_3892_ijmm_2018_3857 crossref_primary_10_1016_j_bbcan_2017_10_006 crossref_primary_10_3390_ijms20215370 crossref_primary_10_1016_j_semcancer_2016_09_001 crossref_primary_10_3390_ijms20112704 crossref_primary_10_1080_15384101_2015_1022697 crossref_primary_10_3390_cancers14235912 crossref_primary_10_1002_mc_22882 crossref_primary_10_1007_s12272_018_1098_z crossref_primary_10_18632_oncotarget_11364 crossref_primary_10_1021_acs_jmedchem_6b00453 crossref_primary_10_1016_j_semcancer_2015_11_001 crossref_primary_10_1016_j_gene_2014_08_020 crossref_primary_10_1371_journal_pone_0160835 crossref_primary_10_4161_cc_26173 crossref_primary_10_1186_s13058_022_01504_4 crossref_primary_10_3892_ol_2022_13239 crossref_primary_10_3390_ijms231911745 crossref_primary_10_3389_fphar_2024_1367981 crossref_primary_10_1016_j_gene_2016_02_015 crossref_primary_10_18632_oncotarget_5424 crossref_primary_10_3389_fphar_2019_00203 crossref_primary_10_1002_stem_3101 crossref_primary_10_3390_biom10081118 crossref_primary_10_1158_0008_5472_CAN_16_2834 crossref_primary_10_4161_cc_24479 crossref_primary_10_3390_cancers12061436 crossref_primary_10_1007_s12032_015_0655_2 crossref_primary_10_1186_s12935_019_0869_z crossref_primary_10_1016_j_bcp_2023_115550 crossref_primary_10_4252_wjsc_v11_i9_693 crossref_primary_10_1007_s12015_021_10216_9 crossref_primary_10_3390_ijerph18073575 crossref_primary_10_3390_ijms23105700 crossref_primary_10_3389_fonc_2020_537930 crossref_primary_10_1007_s00280_019_04010_1 crossref_primary_10_1186_s13046_018_0784_5 crossref_primary_10_18632_oncotarget_6328 crossref_primary_10_18632_oncotarget_14041 crossref_primary_10_1016_j_ajpath_2016_01_006 crossref_primary_10_3892_ol_2016_4587 crossref_primary_10_1007_s11517_021_02324_y crossref_primary_10_18632_genesandcancer_87 crossref_primary_10_1093_abbs_gmt123 crossref_primary_10_1016_j_molmet_2022_101529 crossref_primary_10_1186_s40170_021_00263_8 crossref_primary_10_1016_j_yexcr_2014_04_021 crossref_primary_10_1080_10408398_2018_1551778 crossref_primary_10_1186_1471_2164_15_752 crossref_primary_10_3389_fonc_2022_955892 |
Cites_doi | 10.1007/s10549-010-1076-8 10.1046/j.1524-4741.1999.00136.x 10.1016/j.ygyno.2005.05.045 10.1093/jnci/djj505 10.1016/j.jhep.2008.07.036 10.1016/j.advenzreg.2006.01.004 10.1002/jcb.10708 10.1158/0008-5472.CAN-11-1678 10.1158/0008-5472.CAN-06-4608 10.1158/1541-7786.MCR-11-0206 10.1016/S0092-8674(00)80213-5 10.1152/ajprenal.00136.2011 10.1002/ijc.22202 10.1093/jnci/85.21.1725 10.1136/bmj.e797 10.3233/BD-2007-26108 10.1038/nrc2222 10.1158/0008-5472.CAN-07-2489 10.1016/j.suronc.2009.01.004 10.1172/JCI0215593 10.1093/jnci/djp030 10.4161/cc.4.3.1249 10.1158/0008-5472.CAN-08-2023 10.1073/pnas.0931261100 10.1007/s10549-010-1300-6 10.1006/excr.1998.4154 10.1053/hupa.2000.9842 10.2174/157489212799972891 10.1034/j.1600-065X.2003.00012.x 10.1023/A:1006491619920 10.1097/01.mco.0000232893.21050.15 10.1038/385544a0 10.1073/pnas.0530291100 10.1242/jcs.01069 10.1097/01.mco.0000232894.28674.30 10.1158/0008-5472.CAN-05-3197 10.4161/cc.6.23.4996 10.1016/S0163-7827(01)00010-8 10.1111/j.1365-2184.2007.00498.x 10.1186/bcr2104 |
ContentType | Journal Article |
Copyright | Macmillan Publishers Limited 2013 COPYRIGHT 2013 Nature Publishing Group Copyright Nature Publishing Group Oct 17, 2013 Macmillan Publishers Limited 2013. |
Copyright_xml | – notice: Macmillan Publishers Limited 2013 – notice: COPYRIGHT 2013 Nature Publishing Group – notice: Copyright Nature Publishing Group Oct 17, 2013 – notice: Macmillan Publishers Limited 2013. |
DBID | CGR CUY CVF ECM EIF NPM AAYXX CITATION 3V. 7TM 7TO 7U9 7X7 7XB 88A 88E 8AO 8C1 8FD 8FE 8FH 8FI 8FJ 8FK 8G5 ABUWG AFKRA AZQEC BBNVY BENPR BHPHI CCPQU DWQXO FR3 FYUFA GHDGH GNUQQ GUQSH H94 HCIFZ K9. LK8 M0S M1P M2O M7P MBDVC P64 PQEST PQQKQ PQUKI PRINS Q9U RC3 |
DOI | 10.1038/onc.2012.519 |
DatabaseName | Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed CrossRef ProQuest Central (Corporate) Nucleic Acids Abstracts Oncogenes and Growth Factors Abstracts Virology and AIDS Abstracts ProQuest - Health & Medical Complete保健、医学与药学数据库 ProQuest Central (purchase pre-March 2016) Biology Database (Alumni Edition) Medical Database (Alumni Edition) ProQuest Pharma Collection Public Health Database (ProQuest Medical & Health Databases) Technology Research Database ProQuest SciTech Collection ProQuest Natural Science Collection Hospital Premium Collection Hospital Premium Collection (Alumni Edition) ProQuest Central (Alumni) (purchase pre-March 2016) Research Library (Alumni Edition) ProQuest Central (Alumni) ProQuest Central UK/Ireland ProQuest Central Essentials Biological Science Collection ProQuest Central ProQuest Natural Science Collection ProQuest One Community College ProQuest Central Engineering Research Database Health Research Premium Collection Health Research Premium Collection (Alumni) ProQuest Central Student Research Library Prep AIDS and Cancer Research Abstracts SciTech Premium Collection (Proquest) (PQ_SDU_P3) ProQuest Health & Medical Complete (Alumni) Biological Sciences Health & Medical Collection (Alumni Edition) PML(ProQuest Medical Library) ProQuest research library Biological Science Database Research Library (Corporate) Biotechnology and BioEngineering Abstracts ProQuest One Academic Eastern Edition (DO NOT USE) ProQuest One Academic ProQuest One Academic UKI Edition ProQuest Central China ProQuest Central Basic Genetics Abstracts |
DatabaseTitle | MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) CrossRef Research Library Prep ProQuest Central Student Oncogenes and Growth Factors Abstracts Technology Research Database ProQuest Central Essentials Nucleic Acids Abstracts ProQuest Health & Medical Complete (Alumni) ProQuest Central (Alumni Edition) SciTech Premium Collection ProQuest One Community College Research Library (Alumni Edition) ProQuest Natural Science Collection ProQuest Pharma Collection ProQuest Central China ProQuest Biology Journals (Alumni Edition) ProQuest Central Genetics Abstracts Health Research Premium Collection Health and Medicine Complete (Alumni Edition) Natural Science Collection ProQuest Central Korea Biological Science Collection AIDS and Cancer Research Abstracts ProQuest Research Library ProQuest Medical Library (Alumni) ProQuest Public Health Virology and AIDS Abstracts ProQuest Biological Science Collection ProQuest Central Basic ProQuest One Academic Eastern Edition ProQuest Hospital Collection Health Research Premium Collection (Alumni) Biological Science Database ProQuest SciTech Collection ProQuest Hospital Collection (Alumni) Biotechnology and BioEngineering Abstracts ProQuest Health & Medical Complete ProQuest Medical Library ProQuest One Academic UKI Edition Engineering Research Database ProQuest One Academic ProQuest Central (Alumni) |
DatabaseTitleList | MEDLINE Research Library Prep Research Library Prep AIDS and Cancer Research Abstracts |
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 – sequence: 3 dbid: BENPR name: ProQuest Central url: https://www.proquest.com/central sourceTypes: Aggregation Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine Chemistry Biology |
EISSN | 1476-5594 |
EndPage | 5122 |
ExternalDocumentID | 3101044601 A349722828 10_1038_onc_2012_519 23208501 |
Genre | Research Support, U.S. Gov't, Non-P.H.S Research Support, Non-U.S. Gov't Journal Article Research Support, N.I.H., Extramural |
GrantInformation_xml | – fundername: NCI NIH HHS grantid: R01CA124650-04S1 – fundername: NCI NIH HHS grantid: R01 CA124650 – fundername: NCI NIH HHS grantid: R01CA124650 – fundername: NCI NIH HHS grantid: R01CA129000 – fundername: NCI NIH HHS grantid: R01 CA129000 |
GroupedDBID | --- -Q- 0R~ 123 29N 2WC 36B 39C 3V. 4.4 406 53G 5RE 70F 7X7 88A 88E 8AO 8C1 8FE 8FH 8FI 8FJ 8G5 8R4 8R5 AANZL AAWBL AAZLF ABAKF ABAWZ ABDBF ABJNI ABLJU ABUWG ABZZP ACAOD ACGFO ACGFS ACKTT ACMJI ACPRK ACRQY ACZOJ ADBBV ADFRT ADHDB AEJRE AEMSY AENEX AEVLU AEXYK AFBBN AFKRA AFSHS AGEZK AGHAI AGQEE AHMBA AHSBF AILAN AJRNO ALFFA ALIPV ALMA_UNASSIGNED_HOLDINGS AMYLF ASPBG AVWKF AXYYD AZFZN AZQEC B0M BBNVY BENPR BHPHI BKKNO BPHCQ BVXVI CCPQU CS3 DIK DNIVK DPUIP DU5 DWQXO E3Z EAD EAP EBC EBD EBLON EBS EE. EIOEI EJD EMB EMK EMOBN EPL ESX F5P FDQFY FEDTE FERAY FIZPM FRP FSGXE FYUFA GNUQQ GUQSH HCIFZ HMCUK HVGLF HZ~ IAO IHR INH INR ITC IWAJR JSO JZLTJ KQ8 L7B LK8 M0L M1P M2O M7P N9A NAO NQJWS NXXTH O9- OK1 OVD P2P PQQKQ PROAC PSQYO Q2X RNT RNTTT SNX SNYQT SOHCF SRMVM SV3 SWTZT TAOOD TBHMF TDRGL TEORI TSG TUS UKHRP W2D WH7 ~8M AAYZH CGR CUY CVF ECM EIF NPM AAYXX CITATION AATNV 7TM 7TO 7U9 7XB 8FD 8FK FR3 H94 K9. MBDVC P64 PQEST PQUKI PRINS Q9U RC3 |
ID | FETCH-LOGICAL-c523t-9c95cda77a2857543f933ab5fcf6816c60fbddd6df7320cc1f83ca6c333059d73 |
IEDL.DBID | BENPR |
ISSN | 0950-9232 |
IngestDate | Fri Oct 25 07:13:22 EDT 2024 Thu Oct 10 17:14:01 EDT 2024 Thu Oct 10 18:06:22 EDT 2024 Wed Aug 07 18:48:10 EDT 2024 Tue Aug 06 04:51:42 EDT 2024 Fri Sep 27 02:37:19 EDT 2024 Tue Oct 15 23:49:14 EDT 2024 Fri Oct 11 20:47:10 EDT 2024 |
IsDoiOpenAccess | false |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 42 |
Keywords | breast cancer apoptosis lipogenesis stem-like cells ductal carcinoma resveratrol |
Language | English |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c523t-9c95cda77a2857543f933ab5fcf6816c60fbddd6df7320cc1f83ca6c333059d73 |
Notes | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
OpenAccessLink | https://www.nature.com/articles/onc2012519.pdf |
PMID | 23208501 |
PQID | 1442476056 |
PQPubID | 36330 |
PageCount | 12 |
ParticipantIDs | proquest_miscellaneous_1448214751 proquest_journals_2641525091 proquest_journals_1442476056 gale_infotracmisc_A349722828 gale_infotracacademiconefile_A349722828 crossref_primary_10_1038_onc_2012_519 pubmed_primary_23208501 springer_journals_10_1038_onc_2012_519 |
PublicationCentury | 2000 |
PublicationDate | 2013-10-17 |
PublicationDateYYYYMMDD | 2013-10-17 |
PublicationDate_xml | – month: 10 year: 2013 text: 2013-10-17 day: 17 |
PublicationDecade | 2010 |
PublicationPlace | London |
PublicationPlace_xml | – name: London – name: England – name: New York |
PublicationTitle | Oncogene |
PublicationTitleAbbrev | Oncogene |
PublicationTitleAlternate | Oncogene |
PublicationYear | 2013 |
Publisher | Nature Publishing Group UK Nature Publishing Group |
Publisher_xml | – name: Nature Publishing Group UK – name: Nature Publishing Group |
References | Miller, Soule, Tait, Pauley, Wolman, Dawson (CR17) 1993; 85 Gu, Yuan, Wills, Kasper (CR44) 2007; 67 Al-Hajj, Wicha, Benito-Hernandez, Morrison, Clarke (CR14) 2003; 100 Esslimani-Sahla, Thezenas, Siminy-Lafontaine, Kramar, Lavaill, Chalbos (CR25) 2007; 120 Allan, Vantyghem, Tuck, Chambers (CR45) 2007; 26 Ma, Salunga, Tuggle, Gaudet, Enright, McQuary (CR3) 2003; 100 Carón, Yacoub, Mitchell, Zhu, Hong, Sasazuki (CR33) 2005; 4 Vazquez-Martin, Colomer, Brunet, Lupu, Menendez (CR34) 2008; 41 Kauffmann-Zeh, Rodriguez-Viciana, Ulrich, Gilbert, Coffer, Downward (CR32) 1997; 385 Porter, Krop, Nasser, Sgroi, Kaelin, Marks (CR2) 2001; 61 Menendez, Lupu (CR4) 2007; 7 Pandey, Okuda, Watabe, Pai, Liu, Kobayashi (CR11) 2011; 130 Liu, Furuta, Shindo, Watabe, Xing, Pandey (CR13) 2011; 128 Valverde, Navarro, Benito, Lorenzo (CR35) 1998; 243 Barnes, Ooi, Yarnold, Bundred (CR1) 2012; 344 Milgraum, Witters, Pasternack, Kuhajda (CR8) 1997; 3 Baron, Migita, Tang, Loda (CR27) 2004; 91 Menendez, Lupu (CR24) 2006; 9 Alberola-Ila, Hernandez-Hoyos (CR29) 2003; 191 Bandyopadhyay, Zhan, Wang, Pai, Hirota, Hosobe (CR10) 2006; 66 Pizer, Chrest, Di Giuseppe, Han (CR9) 1998; 58 Pandey, Liu, Xing, Fukuda, Watabe (CR12) 2012; 7 Brown, Goldstein (CR19) 1997; 89 Heppner, Wolman (CR15) 1999; 5 Dawson, Wolman, Tait, Heppner, Miller (CR16) 1996; 148 Rashid, Pizer, Moga (CR7) 1997; 150 Piyathilake, Frost, Manne, Bell, Weiss, Heimburger (CR26) 2000; 31 Horton, Goldstein, Brown (CR6) 2002; 109 Yamashita, Honda, Takatori, Nishino, Minato, Takamura (CR20) 2009; 50 Migita, Ruiz, Fornari, Fiorentino, Priolo, Zadra (CR28) 2009; 101 Diehn, Clarke (CR43) 2006; 98 Lee, Shrieve, Zempolich, Lee, Hammond, Handrahan (CR40) 2005; 99 Guillet-Deniau, Pichard, Koné, Esnous, Nieruchalski, Girard (CR36) 2004; 117 Huang, Li, Liu, Lin, Chung (CR21) 2012; 10 Von Lintig, Dreilinger, Varki, Wallace, Casteel, Boss (CR39) 2000; 62 Chuthapisith, Eremin, El-Sheemey, Eremin (CR41) 2010; 19 Shimano (CR18) 2001; 40 Okuda, Kobayashi, Xia, Watabe, Pai, Hirota (CR46) 2012; 72 Furuta, Pai, Zhan, Bandyopadhyay, Watabe, Mo (CR22) 2008; 68 Uttarwar, Gao, Ingram, Krepinsky (CR37) 2012; 302 Janes, Daly, deFazio, Sutherland (CR38) 1994; 9 Dallas, Xia, Fan, Gray, Gaur, Van Buren (CR42) 2009; 69 Swinnen, Brusselmans, Verhoeven (CR5) 2006; 9 McCubrey, Steelman, Abrams, Lee, Chang, Bertrand (CR31) 2006; 46 Damonte, Hodgson, Chen, Young, Cardiff, Borowsky (CR23) 2008; 10 Ramjaun, Downward (CR30) 2007; 6 E Furuta (BFonc2012519_CR22) 2008; 68 JA Menendez (BFonc2012519_CR24) 2006; 9 CJ Piyathilake (BFonc2012519_CR26) 2000; 31 JD Horton (BFonc2012519_CR6) 2002; 109 T Yamashita (BFonc2012519_CR20) 2009; 50 PR Pandey (BFonc2012519_CR11) 2011; 130 PR Pandey (BFonc2012519_CR12) 2012; 7 JA Menendez (BFonc2012519_CR4) 2007; 7 J Alberola-Ila (BFonc2012519_CR29) 2003; 191 LZ Milgraum (BFonc2012519_CR8) 1997; 3 WC Huang (BFonc2012519_CR21) 2012; 10 NA Dallas (BFonc2012519_CR42) 2009; 69 FC Von Lintig (BFonc2012519_CR39) 2000; 62 L Uttarwar (BFonc2012519_CR37) 2012; 302 NL Barnes (BFonc2012519_CR1) 2012; 344 CM Lee (BFonc2012519_CR40) 2005; 99 G Gu (BFonc2012519_CR44) 2007; 67 A Kauffmann-Zeh (BFonc2012519_CR32) 1997; 385 PJ Dawson (BFonc2012519_CR16) 1996; 148 A Vazquez-Martin (BFonc2012519_CR34) 2008; 41 A Rashid (BFonc2012519_CR7) 1997; 150 ES Pizer (BFonc2012519_CR9) 1998; 58 T Migita (BFonc2012519_CR28) 2009; 101 A Baron (BFonc2012519_CR27) 2004; 91 AR Ramjaun (BFonc2012519_CR30) 2007; 6 M Esslimani-Sahla (BFonc2012519_CR25) 2007; 120 DA Porter (BFonc2012519_CR2) 2001; 61 PW Janes (BFonc2012519_CR38) 1994; 9 AL Allan (BFonc2012519_CR45) 2007; 26 M Al-Hajj (BFonc2012519_CR14) 2003; 100 GH Heppner (BFonc2012519_CR15) 1999; 5 FR Miller (BFonc2012519_CR17) 1993; 85 S Bandyopadhyay (BFonc2012519_CR10) 2006; 66 I Guillet-Deniau (BFonc2012519_CR36) 2004; 117 W Liu (BFonc2012519_CR13) 2011; 128 MS Brown (BFonc2012519_CR19) 1997; 89 JA McCubrey (BFonc2012519_CR31) 2006; 46 H Shimano (BFonc2012519_CR18) 2001; 40 RW Carón (BFonc2012519_CR33) 2005; 4 AM Valverde (BFonc2012519_CR35) 1998; 243 M Diehn (BFonc2012519_CR43) 2006; 98 JV Swinnen (BFonc2012519_CR5) 2006; 9 XJ Ma (BFonc2012519_CR3) 2003; 100 P Damonte (BFonc2012519_CR23) 2008; 10 H Okuda (BFonc2012519_CR46) 2012; 72 S Chuthapisith (BFonc2012519_CR41) 2010; 19 |
References_xml | – volume: 150 start-page: 201 year: 1997 end-page: 208 ident: CR7 article-title: Elevated expression of fatty acid synthase and fatty acid synthetic activity in colorectal neoplasia publication-title: Am J Pathol contributor: fullname: Moga – volume: 128 start-page: 57 year: 2011 end-page: 68 ident: CR13 article-title: Cacalol, a natural sesquiterpene, induces apoptosis in breast cancer cells by modulating Akt-SREBP-FAS signaling pathway publication-title: Breast Cancer Res Treat doi: 10.1007/s10549-010-1076-8 contributor: fullname: Pandey – volume: 5 start-page: 122 year: 1999 end-page: 129 ident: CR15 article-title: MCF-10AT: a model for human breast cancer development publication-title: Breast J doi: 10.1046/j.1524-4741.1999.00136.x contributor: fullname: Wolman – volume: 99 start-page: 415 year: 2005 end-page: 421 ident: CR40 article-title: Correlation between human epidermal growth factor receptor family (EGFR, HER2, HER3, HER4), phosphorylated Akt (P-Akt), and clinical outcomes after radiation therapy in carcinoma of the cervix publication-title: Gynecol Oncol doi: 10.1016/j.ygyno.2005.05.045 contributor: fullname: Handrahan – volume: 98 start-page: 1755 year: 2006 end-page: 1757 ident: CR43 article-title: Cancer stem cells and radiotherapy: new insights into tumor radioresistance publication-title: J Natl Cancer Inst doi: 10.1093/jnci/djj505 contributor: fullname: Clarke – volume: 148 start-page: 313 year: 1996 end-page: 319 ident: CR16 article-title: MCF10AT: a model for the evolution of cancer from proliferative breast disease publication-title: Am J Pathol contributor: fullname: Miller – volume: 50 start-page: 100 year: 2009 end-page: 110 ident: CR20 article-title: Activation of lipogenic pathway correlates with cell proliferation and poor prognosis in hepatocellular carcinoma publication-title: J Hepatol doi: 10.1016/j.jhep.2008.07.036 contributor: fullname: Takamura – volume: 46 start-page: 249 year: 2006 end-page: 279 ident: CR31 article-title: Roles of the RAF/MEK/ERK and PI3K/PTEN/AKT pathways in malignant transformation and drug resistance publication-title: Adv Enzyme Regul doi: 10.1016/j.advenzreg.2006.01.004 contributor: fullname: Bertrand – volume: 91 start-page: 47 year: 2004 end-page: 53 ident: CR27 article-title: Fatty acid synthase: a metabolic oncogene in prostate cancer? publication-title: J Cell Biochem doi: 10.1002/jcb.10708 contributor: fullname: Loda – volume: 72 start-page: 537 year: 2012 end-page: 547 ident: CR46 article-title: Hyaluronan synthase HAS2 promotes tumor progression in bone by stimulating the interaction of breast cancer stem-like cells with macrophages and stromal cells publication-title: Cancer Res doi: 10.1158/0008-5472.CAN-11-1678 contributor: fullname: Hirota – volume: 67 start-page: 4807 year: 2007 end-page: 4815 ident: CR44 article-title: Prostate cancer cells with stem cell characteristics reconstitute the original human tumor publication-title: Cancer Res doi: 10.1158/0008-5472.CAN-06-4608 contributor: fullname: Kasper – volume: 10 start-page: 133 year: 2012 end-page: 142 ident: CR21 article-title: Activation of androgen receptor, lipogenesis, and oxidative stress converged by SREBP-1 is responsible for regulating growth and progression of prostate cancer cells publication-title: Mol Cancer Res doi: 10.1158/1541-7786.MCR-11-0206 contributor: fullname: Chung – volume: 89 start-page: 331 year: 1997 end-page: 340 ident: CR19 article-title: The SREBP pathway: regulation of cholesterol metabolism by proteolysis of a membrane-bound transcription factor publication-title: Cell doi: 10.1016/S0092-8674(00)80213-5 contributor: fullname: Goldstein – volume: 3 start-page: 2115 year: 1997 end-page: 2120 ident: CR8 article-title: Enzymes of the fatty acid synthesis pathway are highly expressed in in situ breast carcinoma publication-title: Clin Cancer Res contributor: fullname: Kuhajda – volume: 302 start-page: 329 year: 2012 end-page: 341 ident: CR37 article-title: SREBP-1 activation by glucose mediates TGF-β upregulation in mesangial cells publication-title: Am J Physiol Renal Physiol doi: 10.1152/ajprenal.00136.2011 contributor: fullname: Krepinsky – volume: 120 start-page: 224 year: 2007 end-page: 229 ident: CR25 article-title: Increased expression of fatty acid synthase and progesterone receptor in early steps of human mammary carcinogenesis publication-title: Int J Cancer doi: 10.1002/ijc.22202 contributor: fullname: Chalbos – volume: 61 start-page: 5697 year: 2001 end-page: 5702 ident: CR2 article-title: A SAGE (serial analysis of gene expression) view of breast tumor progression publication-title: Cancer Res contributor: fullname: Marks – volume: 85 start-page: 1725 year: 1993 end-page: 1732 ident: CR17 article-title: Xenograft model of progressive human proliferative breast disease publication-title: J Natl Cancer Inst doi: 10.1093/jnci/85.21.1725 contributor: fullname: Dawson – volume: 344 start-page: e797 year: 2012 ident: CR1 article-title: Ductal carcinoma in situ of the breast publication-title: BMJ doi: 10.1136/bmj.e797 contributor: fullname: Bundred – volume: 26 start-page: 87 year: 2007 end-page: 98 ident: CR45 article-title: Tumor dormancy and cancer stem cells: implications for the biology and treatment of breast cancer metastasis publication-title: Breast Dis doi: 10.3233/BD-2007-26108 contributor: fullname: Chambers – volume: 7 start-page: 763 year: 2007 end-page: 777 ident: CR4 article-title: Fatty acid synthase and the lipogenic phenotype in cancer pathogenesis publication-title: Nat Rev Cancer doi: 10.1038/nrc2222 contributor: fullname: Lupu – volume: 68 start-page: 1003 year: 2008 end-page: 1011 ident: CR22 article-title: Fatty acid synthase gene is up-regulated by hypoxia via activation of Akt and sterol regulatory element binding protein-1 publication-title: Cancer Res doi: 10.1158/0008-5472.CAN-07-2489 contributor: fullname: Mo – volume: 19 start-page: 27 year: 2010 end-page: 32 ident: CR41 article-title: Breast cancer chemoresistance: emerging importance of cancer stem cells publication-title: Surg Oncol doi: 10.1016/j.suronc.2009.01.004 contributor: fullname: Eremin – volume: 109 start-page: 1125 year: 2002 end-page: 1131 ident: CR6 article-title: SREBPs: activators of the complete program of cholesterol and fatty acid synthesis in the liver publication-title: J Clin Invest doi: 10.1172/JCI0215593 contributor: fullname: Brown – volume: 101 start-page: 519 year: 2009 end-page: 532 ident: CR28 article-title: Fatty acid synthase: a metabolic enzyme and candidate oncogene in prostate cancer publication-title: J Natl Cancer Inst doi: 10.1093/jnci/djp030 contributor: fullname: Zadra – volume: 4 start-page: 456 year: 2005 end-page: 464 ident: CR33 article-title: Radiation-stimulated ERK1/2 and JNK1/2 signaling can promote cell cycle progression in human colon cancer cells publication-title: Cell Cycle doi: 10.4161/cc.4.3.1249 contributor: fullname: Sasazuki – volume: 9 start-page: 3601 year: 1994 end-page: 3608 ident: CR38 article-title: Activation of the Ras signaling pathway in human breast cancer cells overexpressing erbB-2 publication-title: Oncogene contributor: fullname: Sutherland – volume: 69 start-page: 1951 year: 2009 end-page: 1957 ident: CR42 article-title: Chemoresistant colorectal cancer cells, the cancer stem cell phenotype, and increased sensitivity to insulin-like growth factor-I receptor inhibition publication-title: Cancer Res doi: 10.1158/0008-5472.CAN-08-2023 contributor: fullname: Van Buren – volume: 100 start-page: 5974 year: 2003 end-page: 5979 ident: CR3 article-title: Gene expression profiles of human breast cancer progression publication-title: Proc Natl Acad Sci USA doi: 10.1073/pnas.0931261100 contributor: fullname: McQuary – volume: 58 start-page: 4611 year: 1998 end-page: 4615 ident: CR9 article-title: Pharmacological inhibitors of mammalian fatty acid synthase suppress DNA replication and induce apoptosis in tumor cell lines publication-title: Cancer Res contributor: fullname: Han – volume: 130 start-page: 387 year: 2011 end-page: 398 ident: CR11 article-title: Resveratrol suppresses growth of cancer stem-like cells by inhibiting fatty acid synthase publication-title: Breast Cancer Res Treat doi: 10.1007/s10549-010-1300-6 contributor: fullname: Kobayashi – volume: 243 start-page: 274 year: 1998 end-page: 281 ident: CR35 article-title: H-ras induces glucose uptake in brown adipocytes in an insulin- and phosphatidylinositol 3-kinase-independent manner publication-title: Exp Cell Res doi: 10.1006/excr.1998.4154 contributor: fullname: Lorenzo – volume: 31 start-page: 1068 year: 2000 end-page: 1073 ident: CR26 article-title: The expression of fatty acid synthase (FASE) is an early event in the development and progression of squamous cell carcinoma of the lung publication-title: Hum Pathol doi: 10.1053/hupa.2000.9842 contributor: fullname: Heimburger – volume: 7 start-page: 185 year: 2012 end-page: 197 ident: CR12 article-title: Anti-cancer drugs targeting fatty acid synthase (FAS) publication-title: Recent Pat Anticancer Drug Discov doi: 10.2174/157489212799972891 contributor: fullname: Watabe – volume: 191 start-page: 79 year: 2003 end-page: 96 ident: CR29 article-title: The Ras/MAPK cascade and the control of positive selection publication-title: Immunol Rev doi: 10.1034/j.1600-065X.2003.00012.x contributor: fullname: Hernandez-Hoyos – volume: 62 start-page: 51 year: 2000 end-page: 62 ident: CR39 article-title: Ras activation in human breast cancer publication-title: Breast Cancer Res Treat doi: 10.1023/A:1006491619920 contributor: fullname: Boss – volume: 9 start-page: 346 year: 2006 end-page: 357 ident: CR24 article-title: Oncogenic properties of the endogenous fatty acid metabolism: Molecular pathology of fatty acid synthase in cancer cells publication-title: Curr Opin Clin Nutr Metab Care doi: 10.1097/01.mco.0000232893.21050.15 contributor: fullname: Lupu – volume: 385 start-page: 544 year: 1997 end-page: 548 ident: CR32 article-title: Suppression of c-Myc-induced apoptosis by Ras signalling through PI (3) K and PKB publication-title: Nature doi: 10.1038/385544a0 contributor: fullname: Downward – volume: 100 start-page: 3983 year: 2003 end-page: 3988 ident: CR14 article-title: Prospective identification of tumorigenic breast cancer cells publication-title: Proc Natl Acad Sci USA doi: 10.1073/pnas.0530291100 contributor: fullname: Clarke – volume: 117 start-page: 1937 year: 2004 end-page: 1944 ident: CR36 article-title: Glucose induces de novo lipogenesis in rat muscle satellite cells through a sterol-regulatory-element-binding-protein-1c-dependent pathway publication-title: J Cell Sci doi: 10.1242/jcs.01069 contributor: fullname: Girard – volume: 9 start-page: 358 year: 2006 end-page: 365 ident: CR5 article-title: Increased lipogenesis in cancer cells: new players, novel targets publication-title: Curr Opin Clin Nutr Metab Care doi: 10.1097/01.mco.0000232894.28674.30 contributor: fullname: Verhoeven – volume: 66 start-page: 5934 year: 2006 end-page: 5940 ident: CR10 article-title: Mechanism of apoptosis induced by the inhibition of fatty acid synthase in breast cancer cells publication-title: Cancer Res doi: 10.1158/0008-5472.CAN-05-3197 contributor: fullname: Hosobe – volume: 6 start-page: 2902 year: 2007 end-page: 2905 ident: CR30 article-title: Ras and phosphoinositide 3-kinase: partners in development and tumorigenesis publication-title: Cell Cycle doi: 10.4161/cc.6.23.4996 contributor: fullname: Downward – volume: 40 start-page: 439 year: 2001 end-page: 452 ident: CR18 article-title: Sterol regulatory element-binding proteins (SREBPs): transcriptional regulators of lipid synthetic genes publication-title: Prog Lipid Res doi: 10.1016/S0163-7827(01)00010-8 contributor: fullname: Shimano – volume: 41 start-page: 59 year: 2008 end-page: 85 ident: CR34 article-title: Overexpression of fatty acid synthase gene activates HER1/HER2 tyrosine kinase receptors in human breast epithelial cells publication-title: Cell prolif doi: 10.1111/j.1365-2184.2007.00498.x contributor: fullname: Menendez – volume: 10 start-page: R50 year: 2008 ident: CR23 article-title: Mammary carcinoma behavior is programmed in the precancer stem cell publication-title: Breast Cancer Res doi: 10.1186/bcr2104 contributor: fullname: Borowsky – volume: 5 start-page: 122 year: 1999 ident: BFonc2012519_CR15 publication-title: Breast J doi: 10.1046/j.1524-4741.1999.00136.x contributor: fullname: GH Heppner – volume: 385 start-page: 544 year: 1997 ident: BFonc2012519_CR32 publication-title: Nature doi: 10.1038/385544a0 contributor: fullname: A Kauffmann-Zeh – volume: 243 start-page: 274 year: 1998 ident: BFonc2012519_CR35 publication-title: Exp Cell Res doi: 10.1006/excr.1998.4154 contributor: fullname: AM Valverde – volume: 67 start-page: 4807 year: 2007 ident: BFonc2012519_CR44 publication-title: Cancer Res doi: 10.1158/0008-5472.CAN-06-4608 contributor: fullname: G Gu – volume: 61 start-page: 5697 year: 2001 ident: BFonc2012519_CR2 publication-title: Cancer Res contributor: fullname: DA Porter – volume: 72 start-page: 537 year: 2012 ident: BFonc2012519_CR46 publication-title: Cancer Res doi: 10.1158/0008-5472.CAN-11-1678 contributor: fullname: H Okuda – volume: 69 start-page: 1951 year: 2009 ident: BFonc2012519_CR42 publication-title: Cancer Res doi: 10.1158/0008-5472.CAN-08-2023 contributor: fullname: NA Dallas – volume: 9 start-page: 3601 year: 1994 ident: BFonc2012519_CR38 publication-title: Oncogene contributor: fullname: PW Janes – volume: 85 start-page: 1725 year: 1993 ident: BFonc2012519_CR17 publication-title: J Natl Cancer Inst doi: 10.1093/jnci/85.21.1725 contributor: fullname: FR Miller – volume: 98 start-page: 1755 year: 2006 ident: BFonc2012519_CR43 publication-title: J Natl Cancer Inst doi: 10.1093/jnci/djj505 contributor: fullname: M Diehn – volume: 9 start-page: 346 year: 2006 ident: BFonc2012519_CR24 publication-title: Curr Opin Clin Nutr Metab Care doi: 10.1097/01.mco.0000232893.21050.15 contributor: fullname: JA Menendez – volume: 99 start-page: 415 year: 2005 ident: BFonc2012519_CR40 publication-title: Gynecol Oncol doi: 10.1016/j.ygyno.2005.05.045 contributor: fullname: CM Lee – volume: 100 start-page: 5974 year: 2003 ident: BFonc2012519_CR3 publication-title: Proc Natl Acad Sci USA doi: 10.1073/pnas.0931261100 contributor: fullname: XJ Ma – volume: 117 start-page: 1937 year: 2004 ident: BFonc2012519_CR36 publication-title: J Cell Sci doi: 10.1242/jcs.01069 contributor: fullname: I Guillet-Deniau – volume: 302 start-page: 329 year: 2012 ident: BFonc2012519_CR37 publication-title: Am J Physiol Renal Physiol doi: 10.1152/ajprenal.00136.2011 contributor: fullname: L Uttarwar – volume: 109 start-page: 1125 year: 2002 ident: BFonc2012519_CR6 publication-title: J Clin Invest doi: 10.1172/JCI0215593 contributor: fullname: JD Horton – volume: 31 start-page: 1068 year: 2000 ident: BFonc2012519_CR26 publication-title: Hum Pathol doi: 10.1053/hupa.2000.9842 contributor: fullname: CJ Piyathilake – volume: 58 start-page: 4611 year: 1998 ident: BFonc2012519_CR9 publication-title: Cancer Res contributor: fullname: ES Pizer – volume: 9 start-page: 358 year: 2006 ident: BFonc2012519_CR5 publication-title: Curr Opin Clin Nutr Metab Care doi: 10.1097/01.mco.0000232894.28674.30 contributor: fullname: JV Swinnen – volume: 50 start-page: 100 year: 2009 ident: BFonc2012519_CR20 publication-title: J Hepatol doi: 10.1016/j.jhep.2008.07.036 contributor: fullname: T Yamashita – volume: 26 start-page: 87 year: 2007 ident: BFonc2012519_CR45 publication-title: Breast Dis doi: 10.3233/BD-2007-26108 contributor: fullname: AL Allan – volume: 7 start-page: 763 year: 2007 ident: BFonc2012519_CR4 publication-title: Nat Rev Cancer doi: 10.1038/nrc2222 contributor: fullname: JA Menendez – volume: 3 start-page: 2115 year: 1997 ident: BFonc2012519_CR8 publication-title: Clin Cancer Res contributor: fullname: LZ Milgraum – volume: 46 start-page: 249 year: 2006 ident: BFonc2012519_CR31 publication-title: Adv Enzyme Regul doi: 10.1016/j.advenzreg.2006.01.004 contributor: fullname: JA McCubrey – volume: 128 start-page: 57 year: 2011 ident: BFonc2012519_CR13 publication-title: Breast Cancer Res Treat doi: 10.1007/s10549-010-1076-8 contributor: fullname: W Liu – volume: 40 start-page: 439 year: 2001 ident: BFonc2012519_CR18 publication-title: Prog Lipid Res doi: 10.1016/S0163-7827(01)00010-8 contributor: fullname: H Shimano – volume: 62 start-page: 51 year: 2000 ident: BFonc2012519_CR39 publication-title: Breast Cancer Res Treat doi: 10.1023/A:1006491619920 contributor: fullname: FC Von Lintig – volume: 19 start-page: 27 year: 2010 ident: BFonc2012519_CR41 publication-title: Surg Oncol doi: 10.1016/j.suronc.2009.01.004 contributor: fullname: S Chuthapisith – volume: 41 start-page: 59 year: 2008 ident: BFonc2012519_CR34 publication-title: Cell prolif doi: 10.1111/j.1365-2184.2007.00498.x contributor: fullname: A Vazquez-Martin – volume: 68 start-page: 1003 year: 2008 ident: BFonc2012519_CR22 publication-title: Cancer Res doi: 10.1158/0008-5472.CAN-07-2489 contributor: fullname: E Furuta – volume: 91 start-page: 47 year: 2004 ident: BFonc2012519_CR27 publication-title: J Cell Biochem doi: 10.1002/jcb.10708 contributor: fullname: A Baron – volume: 10 start-page: 133 year: 2012 ident: BFonc2012519_CR21 publication-title: Mol Cancer Res doi: 10.1158/1541-7786.MCR-11-0206 contributor: fullname: WC Huang – volume: 150 start-page: 201 year: 1997 ident: BFonc2012519_CR7 publication-title: Am J Pathol contributor: fullname: A Rashid – volume: 344 start-page: e797 year: 2012 ident: BFonc2012519_CR1 publication-title: BMJ doi: 10.1136/bmj.e797 contributor: fullname: NL Barnes – volume: 7 start-page: 185 year: 2012 ident: BFonc2012519_CR12 publication-title: Recent Pat Anticancer Drug Discov doi: 10.2174/157489212799972891 contributor: fullname: PR Pandey – volume: 100 start-page: 3983 year: 2003 ident: BFonc2012519_CR14 publication-title: Proc Natl Acad Sci USA doi: 10.1073/pnas.0530291100 contributor: fullname: M Al-Hajj – volume: 120 start-page: 224 year: 2007 ident: BFonc2012519_CR25 publication-title: Int J Cancer doi: 10.1002/ijc.22202 contributor: fullname: M Esslimani-Sahla – volume: 148 start-page: 313 year: 1996 ident: BFonc2012519_CR16 publication-title: Am J Pathol contributor: fullname: PJ Dawson – volume: 66 start-page: 5934 year: 2006 ident: BFonc2012519_CR10 publication-title: Cancer Res doi: 10.1158/0008-5472.CAN-05-3197 contributor: fullname: S Bandyopadhyay – volume: 130 start-page: 387 year: 2011 ident: BFonc2012519_CR11 publication-title: Breast Cancer Res Treat doi: 10.1007/s10549-010-1300-6 contributor: fullname: PR Pandey – volume: 89 start-page: 331 year: 1997 ident: BFonc2012519_CR19 publication-title: Cell doi: 10.1016/S0092-8674(00)80213-5 contributor: fullname: MS Brown – volume: 10 start-page: R50 year: 2008 ident: BFonc2012519_CR23 publication-title: Breast Cancer Res doi: 10.1186/bcr2104 contributor: fullname: P Damonte – volume: 101 start-page: 519 year: 2009 ident: BFonc2012519_CR28 publication-title: J Natl Cancer Inst doi: 10.1093/jnci/djp030 contributor: fullname: T Migita – volume: 4 start-page: 456 year: 2005 ident: BFonc2012519_CR33 publication-title: Cell Cycle doi: 10.4161/cc.4.3.1249 contributor: fullname: RW Carón – volume: 191 start-page: 79 year: 2003 ident: BFonc2012519_CR29 publication-title: Immunol Rev doi: 10.1034/j.1600-065X.2003.00012.x contributor: fullname: J Alberola-Ila – volume: 6 start-page: 2902 year: 2007 ident: BFonc2012519_CR30 publication-title: Cell Cycle doi: 10.4161/cc.6.23.4996 contributor: fullname: AR Ramjaun |
SSID | ssj0007902 |
Score | 2.4200046 |
Snippet | Upregulation of lipogenesis is a hallmark of cancer and blocking the lipogenic pathway is known to cause tumor cell death by apoptosis. However, the exact role... |
SourceID | proquest gale crossref pubmed springer |
SourceType | Aggregation Database Index Database Publisher |
StartPage | 5111 |
SubjectTerms | 631/67/1059/99 631/67/71 631/80/82/23 692/699/67/1347 Animals Apoptosis Apoptosis - drug effects Biochemistry Breast cancer Breast Neoplasms - metabolism Breast Neoplasms - pathology Breast Neoplasms - prevention & control Cancer Carcinoma, Ductal Carcinoma, Intraductal, Noninfiltrating - metabolism Carcinoma, Intraductal, Noninfiltrating - pathology Carcinoma, Intraductal, Noninfiltrating - prevention & control Care and treatment CD44 antigen Cell Biology Cell culture Cell death Cell Line, Tumor Cell Proliferation Cell surface Cell Survival Ectopic expression Fatty acids Female Gene expression Gene Expression Regulation, Neoplastic - drug effects Genetic aspects Human Genetics Humans Internal Medicine Lipogenesis Lipogenesis - drug effects Lipogenesis - genetics Medicine Medicine & Public Health Mice Mice, Nude Oncology original-article Polyphenols Resveratrol Stem cells Stem Cells - pathology Sterol Regulatory Element Binding Protein 1 - genetics Sterol Regulatory Element Binding Protein 1 - metabolism Stilbenes Surface markers Synthesis Testing Tumors Xenograft Model Antitumor Assays |
Title | Elevated lipogenesis in epithelial stem-like cell confers survival advantage in ductal carcinoma in situ of breast cancer |
URI | https://link.springer.com/article/10.1038/onc.2012.519 https://www.ncbi.nlm.nih.gov/pubmed/23208501 https://www.proquest.com/docview/1442476056 https://www.proquest.com/docview/2641525091 https://search.proquest.com/docview/1448214751 |
Volume | 32 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV3da9swED_WlK17GVv2la0rGuzjSast2Zb9NLqQUgYtY6yQNyPL0gjL7DR2Bv3vd2fLWVrKMPjBZ1u27nQf0ul-AO9Sh26xKQoeCB1z9G8NT02ZcBVngSu1xYP2O59fJGeX0dd5PPcTbo1Pqxx0Yqeoy9rQHPkxGm6C6kHz9nl1xQk1ilZXPYTGHuwLjBTECPa_zC6-fd_qYtVnHaIfEXB0ZYRPfQ9kelxXVMEwFJ9iqrKzY5Ruq-Yd23RrsbSzQaeP4ZF3HtlJz-0ncM9WY7jfw0lej-FgOqC3jeHBuV80fwrXs6X9gy5lyZaLVf2TlNuiYYuK2RVtyFiiBDIq58yXi1-W0Uw-M90-wIY1G9QkKIusSxVoUffQc1QiFq8ZgiGq6t-armE3bVjtWEFJ7i3SUJjWz-DydPZjesY94gI3GJC2PDNZbEqtlBaE3BlJl0mpi9gZl6RhYpLAFSVhUDklRWBM6FJpdGKkRLWRlUo-h1FVV_YlsCw0ZSTKpEhCCsKyTLjCoj9gpRJOGT2B90OX56u-sEbeLYjLNEfW5MSaHFkzgY_Ej5zGW7vWRvttA9gKVa7KT2SUKUGB4wQOb9yJHW5ukgeO5n6cNhj4RCJSGNIld5L_Cd0E3m7J9GJKTatsvelekRLYU4z3vOgFZftDKHFUEhApHwbJ2Wn7jr999f-veA0PBcFxUEaNOoRRu97YN-gUtcUR7Km5wnM6DY_8KPgLpK4MOA |
link.rule.ids | 315,783,787,12070,12237,21402,27938,27939,31733,31734,33280,33281,33758,33759,43324,43593,43819,74081,74350,74638 |
linkProvider | ProQuest |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1Lb9QwELagCMoFwQJloYCReJxMEzuJkxOqqlYLdHtqpb1FztiuVizJdpNF6r9nJo9lW1Uot4zzsGc8D3s8H2MfU49uMRSFCKSJBfq3IFKwidBxFnhrHF503nl6lkwuoh-zeNYvuNV9WuWgE1tFbSugNfIDNNwE1YPm7dvyShBqFO2u9hAa99kDqsNFtfP1bBNwBbrLOUQvIhDoyMg-8T1Q6UFVUv3CUH6NqcbOlkm6rZi3LNOtrdLWAp08ZU9615Efdrx-xu65csQedmCS1yO2ezRgt43Yo2m_Zf6cXR8v3B90KC1fzJfVJam2ec3nJXdLOo6xQPnjVMxZLOa_HKd1fA7tKcCa12vUIyiJvE0UaFDz0HNUIBbvAYEQldVvQ_dwkNa88rygFPcGaShKqxfs4uT4_GgierwFARiONiKDLAZrtDaScDsj5TOlTBF78EkaJpAEvrCEQOW1kgFA6FMFJgGlUGlkVquXbKesSveK8SwEG0mbFElIIViWSV849Aac0tJrMGP2aRjyfNmV1cjb7XCV5sianFiTI2vG7AvxI6fZ1qwMmP7QAH6F6lblhyrKtKSwccz2b7TEAYeb5IGjeT9Lawx7IhlpDOiSO8n_RG7MPmzI9GJKTCtdtW5fkRLUU4xt9jpB2XQIJY4KAiLl8yA5W9--o7ev__8X79nu5Hx6mp9-P_v5hj2WBMxBuTV6n-00q7V7i-5RU7xr58BfUn4MDw |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1Lb9QwEB5BEYVLBctroYCReJzMJnYSJ6eqWroqj1YcqNRb5Dh2teqSLJssUv89M4nTbqsK7S2TzcMznkf8eT6A96nDtNgUBQ-Ejjnmt4anpky4irPAldrij_Y7Hx0nhyfRt9P41OOfGg-rHHxi56jL2tA38gkGbqLqwfA2cR4W8fPLbG_5hxODFK20ejqNu3APo2JMNA7p9AruoXr8IWYUAcekRngQfCDTSV1RL8NQfI6p385GeLrppDei1I1l0y4azR7Bjk8j2X6v98dwx1YjuN8TS16M4MF04HEbwfaRXz5_AhcHC_sXk8uSLebL-ozc3Lxh84rZJW3NWKAtMmrszBfzc8vomz4z3Y7AhjVr9ClolawDDbToheh_1CwWjxkiJKrq35qO4SCtWe1YQXD3FmVoVquncDI7-DU95J57gRssTVuemSw2pVZKC-LwjKTLpNRF7IxL0jAxSeCKktionJIiMCZ0qTQ6MVKiA8lKJZ_BVlVX9gWwLDRlJMqkSEIqx7JMuMJiZmClEk4ZPYYPw5Dny77FRt4tjcs0R9XkpJocVTOGT6SPnGZeu9JG-w0EeBfqYZXvyyhTgkrIMexeOxMH3FwXDxrN_YxtsASKRKSwuEtuFV-Z3xjeXYrpwgRSq2y97i6REu1TjOc87w3l8oXQ4qg5IEo-Dpazce9b3vbl_5_iLWyj-ec_vh5_fwUPBXF0EMxG7cJWu1rb15gptcWbbgr8A7iSEA8 |
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=Elevated+lipogenesis+in+epithelial+stem-like+cell+confers+survival+advantage+in+ductal+carcinoma+in+situ+of+breast+cancer&rft.jtitle=Oncogene&rft.au=Pandey%2C+P+R&rft.au=Xing%2C+F&rft.au=Sharma%2C+S&rft.au=Watabe%2C+M&rft.date=2013-10-17&rft.pub=Nature+Publishing+Group+UK&rft.issn=0950-9232&rft.eissn=1476-5594&rft.volume=32&rft.issue=42&rft.spage=5111&rft.epage=5122&rft_id=info:doi/10.1038%2Fonc.2012.519&rft.externalDocID=10_1038_onc_2012_519 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0950-9232&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0950-9232&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0950-9232&client=summon |