Curcumin converts Foxp3+ regulatory T cells to T helper 1 cells in patients with lung cancer
The regulatory T cells (Treg) play an important role in the tumor tolerance. The methods to regulate the Treg population in cancer‐bearing hosts are limited currently. The effect of curcumin on inhibiting cancer has been recognized, but the mechanism remains elusive. This study tests a hypothesis th...
Saved in:
Published in | Journal of cellular biochemistry Vol. 119; no. 2; pp. 1420 - 1428 |
---|---|
Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Wiley Subscription Services, Inc
01.02.2018
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | The regulatory T cells (Treg) play an important role in the tumor tolerance. The methods to regulate the Treg population in cancer‐bearing hosts are limited currently. The effect of curcumin on inhibiting cancer has been recognized, but the mechanism remains elusive. This study tests a hypothesis that administration of curcumin down regulates Tregs in lung cancer (LC) patients. In this study, a group of LC patients was treated with curcumin. The peripheral Tregs and T helper (Th) 1 cells were analyzed by flow cytometry. The mechanism by which curcumin regulated the Tregs was observed by cell culture approaches. The results showed that the frequency of peripheral Treg was markedly higher in LC patients than that in healthy subjects, which was suppressed after treating with curcumin for 2 weeks. The peripheral Th1 cells were increased in LC patients after the curcumin therapy. The data of the in vitro experiments showed that curcumin converted the LC patient‐isolated Tregs to Th1 cells via repressing the gene transcription of forkhead protein‐3 and increasing the expression of interferon‐γ. In conclusion, curcumin can convert LC patient‐isolated Tregs to Th1 cells. The results suggest that curcumin may improve the antitumor immunity by regulating the tumor specific immune tolerance.
The frequency of peripheral Treg in lung cancer patients was suppressed after treating with curcumin for 2 weeks. The peripheral Th1 cells were increased in lung cancer patients after the curcumin therapy. Curcumin converted the lung cancer‐isolated Tregs to Th1 cells via repressing the gene transcription of forkhead protein‐3 and increasing the expression of interferon‐gamma. |
---|---|
AbstractList | The regulatory T cells (Treg) play an important role in the tumor tolerance. The methods to regulate the Treg population in cancer-bearing hosts are limited currently. The effect of curcumin on inhibiting cancer has been recognized, but the mechanism remains elusive. This study tests a hypothesis that administration of curcumin down regulates Tregs in lung cancer (LC) patients. In this study, a group of LC patients was treated with curcumin. The peripheral Tregs and T helper (Th) 1 cells were analyzed by flow cytometry. The mechanism by which curcumin regulated the Tregs was observed by cell culture approaches. The results showed that the frequency of peripheral Treg was markedly higher in LC patients than that in healthy subjects, which was suppressed after treating with curcumin for 2 weeks. The peripheral Th1 cells were increased in LC patients after the curcumin therapy. The data of the in vitro experiments showed that curcumin converted the LC patient-isolated Tregs to Th1 cells via repressing the gene transcription of forkhead protein-3 and increasing the expression of interferon-γ. In conclusion, curcumin can convert LC patient-isolated Tregs to Th1 cells. The results suggest that curcumin may improve the antitumor immunity by regulating the tumor specific immune tolerance.The regulatory T cells (Treg) play an important role in the tumor tolerance. The methods to regulate the Treg population in cancer-bearing hosts are limited currently. The effect of curcumin on inhibiting cancer has been recognized, but the mechanism remains elusive. This study tests a hypothesis that administration of curcumin down regulates Tregs in lung cancer (LC) patients. In this study, a group of LC patients was treated with curcumin. The peripheral Tregs and T helper (Th) 1 cells were analyzed by flow cytometry. The mechanism by which curcumin regulated the Tregs was observed by cell culture approaches. The results showed that the frequency of peripheral Treg was markedly higher in LC patients than that in healthy subjects, which was suppressed after treating with curcumin for 2 weeks. The peripheral Th1 cells were increased in LC patients after the curcumin therapy. The data of the in vitro experiments showed that curcumin converted the LC patient-isolated Tregs to Th1 cells via repressing the gene transcription of forkhead protein-3 and increasing the expression of interferon-γ. In conclusion, curcumin can convert LC patient-isolated Tregs to Th1 cells. The results suggest that curcumin may improve the antitumor immunity by regulating the tumor specific immune tolerance. The frequency of peripheral Treg in lung cancer patients was suppressed after treating with curcumin for 2 weeks. The peripheral Th1 cells were increased in lung cancer patients after the curcumin therapy. Curcumin converted the lung cancer‐isolated Tregs to Th1 cells via repressing the gene transcription of forkhead protein‐3 and increasing the expression of interferon‐gamma. The regulatory T cells (Treg) play an important role in the tumor tolerance. The methods to regulate the Treg population in cancer‐bearing hosts are limited currently. The effect of curcumin on inhibiting cancer has been recognized, but the mechanism remains elusive. This study tests a hypothesis that administration of curcumin down regulates Tregs in lung cancer (LC) patients. In this study, a group of LC patients was treated with curcumin. The peripheral Tregs and T helper (Th) 1 cells were analyzed by flow cytometry. The mechanism by which curcumin regulated the Tregs was observed by cell culture approaches. The results showed that the frequency of peripheral Treg was markedly higher in LC patients than that in healthy subjects, which was suppressed after treating with curcumin for 2 weeks. The peripheral Th1 cells were increased in LC patients after the curcumin therapy. The data of the in vitro experiments showed that curcumin converted the LC patient‐isolated Tregs to Th1 cells via repressing the gene transcription of forkhead protein‐3 and increasing the expression of interferon‐γ. In conclusion, curcumin can convert LC patient‐isolated Tregs to Th1 cells. The results suggest that curcumin may improve the antitumor immunity by regulating the tumor specific immune tolerance. The frequency of peripheral Treg in lung cancer patients was suppressed after treating with curcumin for 2 weeks. The peripheral Th1 cells were increased in lung cancer patients after the curcumin therapy. Curcumin converted the lung cancer‐isolated Tregs to Th1 cells via repressing the gene transcription of forkhead protein‐3 and increasing the expression of interferon‐gamma. The regulatory T cells (Treg) play an important role in the tumor tolerance. The methods to regulate the Treg population in cancer-bearing hosts are limited currently. The effect of curcumin on inhibiting cancer has been recognized, but the mechanism remains elusive. This study tests a hypothesis that administration of curcumin down regulates Tregs in lung cancer (LC) patients. In this study, a group of LC patients was treated with curcumin. The peripheral Tregs and T helper (Th) 1 cells were analyzed by flow cytometry. The mechanism by which curcumin regulated the Tregs was observed by cell culture approaches. The results showed that the frequency of peripheral Treg was markedly higher in LC patients than that in healthy subjects, which was suppressed after treating with curcumin for 2 weeks. The peripheral Th1 cells were increased in LC patients after the curcumin therapy. The data of the in vitro experiments showed that curcumin converted the LC patient-isolated Tregs to Th1 cells via repressing the gene transcription of forkhead protein-3 and increasing the expression of interferon-γ. In conclusion, curcumin can convert LC patient-isolated Tregs to Th1 cells. The results suggest that curcumin may improve the antitumor immunity by regulating the tumor specific immune tolerance. |
Author | Zeng, Bo Zhu, Hao S. Luo, Hong H. Chen, Zhen G. Lei, Yi Y. Su, Chun H. Zou, Jian Y. |
Author_xml | – sequence: 1 givenname: Jian Y. orcidid: 0000-0003-3835-1626 surname: Zou fullname: Zou, Jian Y. email: jianyongrzou@outlook.com organization: The First Affiliated Hospital of Sun Yat‐Sen University – sequence: 2 givenname: Chun H. surname: Su fullname: Su, Chun H. organization: The First Affiliated Hospital of Sun Yat‐Sen University – sequence: 3 givenname: Hong H. surname: Luo fullname: Luo, Hong H. organization: The First Affiliated Hospital of Sun Yat‐Sen University – sequence: 4 givenname: Yi Y. surname: Lei fullname: Lei, Yi Y. organization: The First Affiliated Hospital of Sun Yat‐Sen University – sequence: 5 givenname: Bo surname: Zeng fullname: Zeng, Bo organization: The First Affiliated Hospital of Sun Yat‐Sen University – sequence: 6 givenname: Hao S. surname: Zhu fullname: Zhu, Hao S. organization: The First Affiliated Hospital of Sun Yat‐Sen University – sequence: 7 givenname: Zhen G. surname: Chen fullname: Chen, Zhen G. organization: Huangpu Branch of The First Affiliated Hospital of Sun Yat‐Sen University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/28731226$$D View this record in MEDLINE/PubMed |
BookMark | eNp1kUtPwzAQhC1URB9w4A8gS1xAKK0faRIfoaI8VIlLuSFZjuO0qRI72Aml_x6XtpcKTrtafTNazfRBRxutALjEaIgRIqOVTIckooicgB5GLA7CKAw7oIdiigJCMemCvnMrhBBjlJyBLklifyVRD3xMWivbqtBQGv2lbOPg1HzX9A5atWhL0Ri7gXMoVVk62Bi_LlVZKwvx_uaVtWgKpb1yXTRLWLZ6AaXQUtlzcJqL0qmL_RyA9-njfPIczN6eXib3s0DSMSUBFVilSGQKy0xIiTOSRoxmY5onaZKylOUkwXEoBI1ZlgucSxHinOZRiDMWZpIOwM3Ot7bms1Wu4VXhtu8JrUzrOGaEjBH1cXj0-ghdmdZq_52nYhZHjGHiqas91aaVynhti0rYDT_k5oHRDpDWOGdVzmXR-BiMbqwoSo4R3zbDfTP8txmvuD1SHEz_Yvfu66JUm_9B_jp52Cl-AFG7m98 |
CitedBy_id | crossref_primary_10_1016_j_semcancer_2022_06_009 crossref_primary_10_3389_fimmu_2023_1102778 crossref_primary_10_3389_fimmu_2024_1343316 crossref_primary_10_1016_j_phymed_2024_156028 crossref_primary_10_3390_pharmaceutics14081589 crossref_primary_10_1016_j_jep_2025_119636 crossref_primary_10_3389_fimmu_2022_1051998 crossref_primary_10_1016_j_phrs_2019_104353 crossref_primary_10_2174_0109298673305616240610153554 crossref_primary_10_1111_jcmm_17936 crossref_primary_10_1002_JLB_3MR0320_444R crossref_primary_10_1093_mutage_geac020 crossref_primary_10_2139_ssrn_4087414 crossref_primary_10_3389_fphar_2024_1289957 crossref_primary_10_3892_etm_2024_12453 crossref_primary_10_1021_acs_molpharmaceut_9b00583 crossref_primary_10_1016_j_imlet_2020_10_008 crossref_primary_10_1055_a_1458_5646 crossref_primary_10_2174_0109298673274796240116105555 crossref_primary_10_1186_s12935_022_02815_4 crossref_primary_10_1002_biof_1716 crossref_primary_10_1002_ptr_7734 crossref_primary_10_3390_nu12041193 crossref_primary_10_1016_j_intimp_2022_109475 crossref_primary_10_3390_pharmaceutics13111879 crossref_primary_10_15789_1563_0625_CEO_2072 crossref_primary_10_3389_fnut_2018_00138 crossref_primary_10_1016_j_canlet_2024_216955 crossref_primary_10_3390_ijms232213732 crossref_primary_10_1016_j_semcancer_2020_05_009 crossref_primary_10_3390_cancers12030673 crossref_primary_10_1007_s10753_022_01678_1 crossref_primary_10_1016_j_bioactmat_2021_03_008 crossref_primary_10_1016_j_biopha_2022_113618 crossref_primary_10_3390_cells10020355 crossref_primary_10_1002_cncr_32041 crossref_primary_10_1055_s_0040_1722380 crossref_primary_10_3390_ijms232314710 crossref_primary_10_1007_s12272_021_01355_1 crossref_primary_10_1016_j_phymed_2023_154986 crossref_primary_10_1016_j_autrev_2019_05_012 crossref_primary_10_1016_j_canlet_2019_06_001 crossref_primary_10_1186_s12943_023_01740_y crossref_primary_10_3389_fimmu_2022_1041138 crossref_primary_10_3390_ijms25010232 crossref_primary_10_1002_ptr_8482 crossref_primary_10_1016_j_biopha_2023_114758 crossref_primary_10_1016_j_pharmthera_2020_107700 crossref_primary_10_1016_j_semcancer_2020_02_011 crossref_primary_10_1016_j_phymed_2018_09_194 crossref_primary_10_1002_biof_1818 crossref_primary_10_3390_biomedicines9091183 crossref_primary_10_4103_japtr_japtr_54_22 crossref_primary_10_1080_10408398_2018_1537237 crossref_primary_10_1111_jfbc_13824 crossref_primary_10_1016_j_jnutbio_2020_108428 crossref_primary_10_1002_biof_1776 crossref_primary_10_12677_TCM_2019_82021 crossref_primary_10_1016_j_prp_2020_153082 crossref_primary_10_3390_ijms20071714 crossref_primary_10_3762_bjnano_12_78 crossref_primary_10_1016_j_actbio_2022_12_066 crossref_primary_10_1016_j_addr_2021_04_015 crossref_primary_10_1016_j_semcancer_2020_09_004 crossref_primary_10_1111_jpn_14029 crossref_primary_10_4110_in_2019_19_e35 crossref_primary_10_1016_j_semcancer_2021_11_006 crossref_primary_10_3390_cancers12113194 crossref_primary_10_1002_jcp_29819 crossref_primary_10_1016_j_fochms_2024_100198 crossref_primary_10_3390_ijms24087647 crossref_primary_10_1155_2022_4355386 crossref_primary_10_1016_j_jconrel_2020_11_047 crossref_primary_10_1016_j_biopha_2020_109946 crossref_primary_10_3390_nu12051417 |
Cites_doi | 10.1016/j.immuni.2015.08.006 10.1023/A:1022951824806 10.1007/s00432-011-1010-4 10.1016/j.intimp.2017.02.017 10.3390/vaccines3030490 10.1038/srep04649 10.1016/j.immuni.2008.05.007 10.1371/journal.pone.0067171 10.1038/nm.3432 10.1080/2162402X.2014.1002723 10.1155/2015/248529 10.4161/onci.1.2.18481 10.1038/cmi.2010.11 10.1371/journal.pone.0062300 10.1016/j.intimp.2012.06.016 10.1007/s10555-015-9566-0 10.1074/jbc.M409024200 10.1038/srep10322 10.1016/j.ijrobp.2015.01.011 10.1016/j.canlet.2015.05.005 10.1097/JTO.0000000000000524 10.1155/2015/824746 10.1080/2162402X.2016.1249553 10.1615/CritRevImmunol.2015013607 10.1166/jbn.2015.2041 10.1016/j.cgh.2015.02.019 10.2174/1389201015666140813122703 10.1111/j.1600-065X.2008.00616.x 10.1016/j.immuni.2015.05.016 10.1158/2326-6066.CIR-13-0138 10.1371/journal.pone.0112346 10.1038/srep10665 10.1371/journal.pone.0134110 10.4049/jimmunol.1202399 |
ContentType | Journal Article |
Copyright | 2017 Wiley Periodicals, Inc. 2018 Wiley Periodicals, Inc. |
Copyright_xml | – notice: 2017 Wiley Periodicals, Inc. – notice: 2018 Wiley Periodicals, Inc. |
DBID | AAYXX CITATION CGR CUY CVF ECM EIF NPM 7QL 7QP 7QR 7T7 7TK 7U9 8FD C1K FR3 H94 K9. M7N P64 7X8 |
DOI | 10.1002/jcb.26302 |
DatabaseName | CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed Bacteriology Abstracts (Microbiology B) Calcium & Calcified Tissue Abstracts Chemoreception Abstracts Industrial and Applied Microbiology Abstracts (Microbiology A) Neurosciences Abstracts Virology and AIDS Abstracts Technology Research Database Environmental Sciences and Pollution Management Engineering Research Database AIDS and Cancer Research Abstracts ProQuest Health & Medical Complete (Alumni) Algology Mycology and Protozoology Abstracts (Microbiology C) Biotechnology and BioEngineering Abstracts MEDLINE - Academic |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) Virology and AIDS Abstracts Technology Research Database ProQuest Health & Medical Complete (Alumni) Neurosciences Abstracts Biotechnology and BioEngineering Abstracts Environmental Sciences and Pollution Management Bacteriology Abstracts (Microbiology B) Algology Mycology and Protozoology Abstracts (Microbiology C) AIDS and Cancer Research Abstracts Chemoreception Abstracts Engineering Research Database Industrial and Applied Microbiology Abstracts (Microbiology A) Calcium & Calcified Tissue Abstracts MEDLINE - Academic |
DatabaseTitleList | MEDLINE - Academic CrossRef MEDLINE Virology and AIDS 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 |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Chemistry Biology |
EISSN | 1097-4644 |
EndPage | 1428 |
ExternalDocumentID | 28731226 10_1002_jcb_26302 JCB26302 |
Genre | article Journal Article |
GroupedDBID | --- -~X .3N .GA .GJ .Y3 05W 0R~ 10A 1L6 1OB 1OC 1ZS 31~ 33P 3SF 3WU 4.4 4ZD 50Y 50Z 51W 51X 52M 52N 52O 52P 52S 52T 52U 52W 52X 53G 5GY 5RE 5VS 66C 702 7PT 8-0 8-1 8-3 8-4 8-5 8UM 930 A03 AAESR AAEVG AAHHS AAHQN AAMNL AANHP AANLZ AAONW AASGY AAXRX AAYCA AAZKR ABCQN ABCUV ABEML ABIJN ABJNI ABPVW ACAHQ ACBWZ ACCFJ ACCZN ACGFO ACGFS ACIWK ACPOU ACPRK ACRPL ACSCC ACXBN ACXQS ACYXJ ADBBV ADEOM ADIZJ ADKYN ADMGS ADNMO ADOZA ADXAS ADZMN ADZOD AEEZP AEGXH AEIGN AEIMD AENEX AEQDE AEUQT AEUYR AFBPY AFFPM AFGKR AFPWT AFRAH AFWVQ AFZJQ AHBTC AHMBA AIAGR AITYG AIURR AIWBW AJBDE AJXKR ALAGY ALMA_UNASSIGNED_HOLDINGS ALUQN ALVPJ AMBMR AMYDB ASPBG ATUGU AUFTA AVWKF AZBYB AZFZN AZVAB BAFTC BDRZF BFHJK BHBCM BLYAC BMNLL BMXJE BNHUX BROTX BRXPI BY8 CS3 D-E D-F DCZOG DPXWK DR1 DR2 DRFUL DRSTM DU5 EBD EBS EJD EMOBN F00 F01 F04 F5P FEDTE G-S G.N GNP GODZA H.T H.X HBH HF~ HGLYW HHY HHZ HVGLF HZ~ IH2 IX1 J0M JPC KQQ LATKE LAW LC2 LC3 LEEKS LH4 LH6 LITHE LOXES LP6 LP7 LUTES LW6 LYRES MEWTI MK4 MRFUL MRSTM MSFUL MSSTM MXFUL MXSTM N04 N05 N9A NDZJH NF~ NNB O66 O9- OIG P2P P2W P2X P4D PALCI PQQKQ Q.N Q11 QB0 QRW R.K RBB RIWAO RJQFR ROL RWI RX1 RYL SAMSI SUPJJ SV3 UB1 V8K W8V W99 WBKPD WIB WIH WIK WJL WNSPC WOHZO WQJ WRC WSB WXSBR WYISQ XG1 XPP XV2 ZGI ZXP ZZTAW ~IA ~WT AAMMB AAYXX AEFGJ AEYWJ AGHNM AGQPQ AGXDD AGYGG AIDQK AIDYY CITATION CGR CUY CVF ECM EIF NPM 7QL 7QP 7QR 7T7 7TK 7U9 8FD C1K FR3 H94 K9. M7N P64 7X8 |
ID | FETCH-LOGICAL-c3532-3a1eb0ade1cdacc1d2b693d53f8b8b9b9f28174aa379dfa1fca41f3f641d94dc3 |
IEDL.DBID | DR2 |
ISSN | 0730-2312 1097-4644 |
IngestDate | Fri Jul 11 03:59:10 EDT 2025 Tue Jul 29 16:30:25 EDT 2025 Wed Feb 19 02:43:48 EST 2025 Thu Apr 24 22:55:15 EDT 2025 Thu Jul 31 00:57:28 EDT 2025 Wed Jan 22 16:31:07 EST 2025 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 2 |
Keywords | lung cancer regulatory T cells T helper 1 cells forkhead box protein-3 Interferon-γ |
Language | English |
License | http://onlinelibrary.wiley.com/termsAndConditions#vor 2017 Wiley Periodicals, Inc. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c3532-3a1eb0ade1cdacc1d2b693d53f8b8b9b9f28174aa379dfa1fca41f3f641d94dc3 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ORCID | 0000-0003-3835-1626 |
PMID | 28731226 |
PQID | 1979769912 |
PQPubID | 1006368 |
PageCount | 9 |
ParticipantIDs | proquest_miscellaneous_1922503073 proquest_journals_1979769912 pubmed_primary_28731226 crossref_citationtrail_10_1002_jcb_26302 crossref_primary_10_1002_jcb_26302 wiley_primary_10_1002_jcb_26302_JCB26302 |
PublicationCentury | 2000 |
PublicationDate | February 2018 2018-02-00 20180201 |
PublicationDateYYYYMMDD | 2018-02-01 |
PublicationDate_xml | – month: 02 year: 2018 text: February 2018 |
PublicationDecade | 2010 |
PublicationPlace | United States |
PublicationPlace_xml | – name: United States – name: Hoboken |
PublicationTitle | Journal of cellular biochemistry |
PublicationTitleAlternate | J Cell Biochem |
PublicationYear | 2018 |
Publisher | Wiley Subscription Services, Inc |
Publisher_xml | – name: Wiley Subscription Services, Inc |
References | 2015; 13 2015; 35 2011; 137 2015; 34 2015; 5 2015; 4 2015; 3 2015a; 42 2015; 92 2015; 364 2017; 46 2015; 10 2008; 222 2012; 14 2013; 8 2014; 20 2016; 5 2014; 4 2004; 279 2012; 1 2014; 2 2015; 20 2008; 29 2015; 43 2015; 2015 2014; 15 2014; 9 2014; 34 2010; 7 2003; 21 2015b; 11 2013; 190 e_1_2_7_6_1 e_1_2_7_5_1 e_1_2_7_4_1 e_1_2_7_3_1 e_1_2_7_9_1 e_1_2_7_8_1 e_1_2_7_7_1 e_1_2_7_19_1 e_1_2_7_18_1 e_1_2_7_17_1 e_1_2_7_16_1 e_1_2_7_15_1 e_1_2_7_14_1 e_1_2_7_13_1 e_1_2_7_12_1 e_1_2_7_11_1 e_1_2_7_10_1 e_1_2_7_26_1 e_1_2_7_27_1 e_1_2_7_28_1 e_1_2_7_29_1 Hanagiri T (e_1_2_7_23_1) 2014; 34 e_1_2_7_30_1 e_1_2_7_25_1 e_1_2_7_31_1 e_1_2_7_24_1 e_1_2_7_32_1 e_1_2_7_33_1 e_1_2_7_22_1 e_1_2_7_34_1 e_1_2_7_21_1 e_1_2_7_35_1 e_1_2_7_20_1 e_1_2_7_36_1 e_1_2_7_37_1 Luo H (e_1_2_7_2_1) 2015; 20 |
References_xml | – volume: 4 start-page: 4649 year: 2014 article-title: Mast cell‐derived serine proteinase regulates T helper 2 polarization publication-title: Sci Rep – volume: 29 start-page: 44 year: 2008 end-page: 56 article-title: Molecular antagonism and plasticity of regulatory and inflammatory T cell programs publication-title: Immunity – volume: 20 start-page: 62 year: 2014 end-page: 68 article-title: Pathogenic conversion of Foxp3+ T cells into TH17 cells in autoimmune arthritis publication-title: Nat Med – volume: 2 start-page: 341 year: 2014 end-page: 350 article-title: Nonclassical antigen‐processing pathways are required for MHC class II‐restricted direct tumor recognition by NY‐ESO‐1‐specific CD4(+) T cells publication-title: Cancer Immunol Res – volume: 3 start-page: 490 year: 2015 end-page: 502 article-title: Interest of tumor‐specific CD4 t helper 1 cells for therapeutic anticancer vaccine publication-title: Vaccines (Basel) – volume: 34 start-page: 277 year: 2015 end-page: 290 article-title: Regulatory T cells and potential inmmunotherapeutic targets in lung cancer publication-title: Cancer Metastasis Rev – volume: 2015 start-page: 248529 year: 2015 article-title: Psychiatric disorders and polyphenols: can they be helpful in therapy publication-title: Oxid Med Cell Longev – volume: 92 start-page: 390 year: 2015 end-page: 398 article-title: Combination effect of regulatory T‐cell depletion and ionizing radiation in mouse models of lung and colon cancer publication-title: Int J Radiat Oncol Biol Phys – volume: 222 start-page: 129 year: 2008 end-page: 144 article-title: Multiple roles for CD4+ T cells in anti‐tumor immune responses publication-title: Immunol Rev – volume: 2015 start-page: 824746 year: 2015 article-title: Encapsulation of curcumin in diblock copolymer micelles for cancer therapy publication-title: Biomed Res Int – volume: 4 start-page: e1002723 year: 2015 article-title: Rapid generation of NY‐ESO‐1‐specific CD4 T1 cells for adoptive T‐cell therapy publication-title: Oncoimmunology – volume: 14 start-page: 99 year: 2012 end-page: 106 article-title: Curcumin inhibits suppressive capacity of naturally occurring CD4+CD25+ regulatory T cells in mice in vitro publication-title: Int Immunopharmacol – volume: 43 start-page: 579 year: 2015 end-page: 590 article-title: Regulatory t cells in tumor‐Associated tertiary lymphoid structures suppress anti‐tumor t cell responses publication-title: Immunity – volume: 190 start-page: 2544 year: 2013 end-page: 2553 article-title: Reduced CD18 levels drive regulatory T cell conversion into Th17 cells in the CD18hypo PL/J mouse model of psoriasis publication-title: J Immunol – volume: 137 start-page: 1525 year: 2011 end-page: 1533 article-title: Cancer‐derived matrix metalloproteinase‐9 contributes to tumor tolerance publication-title: J Cancer Res Clin Oncol – volume: 5 start-page: 10322 year: 2015 article-title: Curcumin‐encapsulated polymeric micelles suppress the development of colon cancer in vitro and in vivo publication-title: Sci Rep – volume: 11 start-page: 1093 year: 2015b end-page: 1105 article-title: Fabrication of curcumin micellar nanoparticles with enhanced anti‐cancer activity publication-title: J Biomed Nanotechnol – volume: 7 start-page: 306 year: 2010 end-page: 315 article-title: Curcumin reverses T cell‐mediated adaptive immune dysfunctions in tumor‐bearing hosts publication-title: Cell Mol Immunol – volume: 21 start-page: 21 year: 2003 end-page: 32 article-title: Reversal of tumor‐induced immunosuppression by TGF‐beta inhibitors publication-title: Invest New Drugs – volume: 5 start-page: e1249553 year: 2016 article-title: CD4+CD25hiCD127‐ Treg and CD4+CD45R0+CD49b+LAG3+ Tr1 cells in bone marrow and peripheral blood samples from children with neuroblastoma publication-title: Oncoimmunology – volume: 13 start-page: 1444 year: 2015 end-page: 1449 article-title: Curcumin in combination with mesalamine induces remission in patients with mild‐to‐moderate ulcerative colitis in a randomized controlled trial publication-title: Clin Gastroenterol Hepatol – volume: 42 start-page: 1062 year: 2015a end-page: 1074 article-title: E3 ubiquitin ligase VHL regulates hypoxia‐Inducible factor‐1alpha to maintain regulatory t cell stability and suppressive capacity publication-title: Immunity – volume: 20 start-page: 791 year: 2015 end-page: 799 article-title: Risk factors for recurrence in patients with resected N1 non‐small cell lung cancer—a systematic review and meta‐analysis publication-title: J Buon – volume: 364 start-page: 135 year: 2015 end-page: 141 article-title: Curcumin inhibits cancer stem cell phenotypes in ex vivo models of colorectal liver metastases, and is clinically safe and tolerable in combination with FOLFOX chemotherapy publication-title: Cancer Lett – volume: 46 start-page: 80 year: 2017 end-page: 86 article-title: Curcumin inhibiting Th17 cell differentiation by regulating the metabotropic glutamate receptor‐4 expression on dendritic cells publication-title: Int Immunopharmacol – volume: 10 start-page: 872 year: 2015 end-page: 882 article-title: Stereotactic ablative radiation therapy for the treatment of early‐stage non‐small‐cell lung cancer: CEPO review and recommendations publication-title: J Thorac Oncol – volume: 8 start-page: e67171 year: 2013 article-title: Curcumin attenuates acute graft‐versus‐host disease severity via in vivo regulations on Th1, Th17 and regulatory T cells publication-title: PLoS ONE – volume: 9 start-page: e112346 year: 2014 article-title: Normocaloric low cholesterol diet modulates Th17/Treg balance in patients with chronic hepatitis C virus infection publication-title: PLoS ONE – volume: 5 start-page: 10665 year: 2015 article-title: Tumor‐specific Th2 responses inhibit growth of CT26 colon‐cancer cells in mice via converting intratumor regulatory T cells to Th9 cells publication-title: Sci Rep – volume: 35 start-page: 153 year: 2015 end-page: 172 article-title: CD8+ t cell‐Independent immune‐Mediated mechanisms of anti‐tumor activity publication-title: Crit Rev Immunol – volume: 10 start-page: e0134110 year: 2015 article-title: Curcumin‐Mediated HDAC inhibition suppresses the DNA damage response and contributes to increased DNA damage sensitivity publication-title: PLoS ONE – volume: 8 start-page: e62300 year: 2013 article-title: Curcumin inhibits CD4(+) T cell activation, but augments CD69 expression and TGF‐beta1‐mediated generation of regulatory T cells at late phase publication-title: PLoS ONE – volume: 34 start-page: 7185 year: 2014 end-page: 7190 article-title: Regulatory T‐cells and micrometastasis in lymph nodes of stage I NSCLC publication-title: Anticancer Res – volume: 1 start-page: 162 year: 2012 end-page: 171 article-title: Tgf‐beta1 produced by activated CD4(+) t cells antagonizes t cell surveillance of tumor development publication-title: Oncoimmunology – volume: 279 start-page: 51163 year: 2004 end-page: 51171 article-title: Curcumin, a novel p300/CREB‐binding protein‐specific inhibitor of acetyltransferase, represses the acetylation of histone/nonhistone proteins and histone acetyltransferase‐dependent chromatin transcription publication-title: J Biol Chem – volume: 15 start-page: 330 year: 2014 end-page: 342 article-title: Dietary polyphenols for treatment of Alzheimer's disease‐future research and development publication-title: Curr Pharm Biotechnol – ident: e_1_2_7_22_1 doi: 10.1016/j.immuni.2015.08.006 – ident: e_1_2_7_4_1 doi: 10.1023/A:1022951824806 – ident: e_1_2_7_5_1 doi: 10.1007/s00432-011-1010-4 – ident: e_1_2_7_37_1 doi: 10.1016/j.intimp.2017.02.017 – ident: e_1_2_7_26_1 doi: 10.3390/vaccines3030490 – ident: e_1_2_7_17_1 doi: 10.1038/srep04649 – ident: e_1_2_7_20_1 doi: 10.1016/j.immuni.2008.05.007 – ident: e_1_2_7_32_1 doi: 10.1371/journal.pone.0067171 – ident: e_1_2_7_36_1 doi: 10.1038/nm.3432 – volume: 34 start-page: 7185 year: 2014 ident: e_1_2_7_23_1 article-title: Regulatory T‐cells and micrometastasis in lymph nodes of stage I NSCLC publication-title: Anticancer Res – ident: e_1_2_7_18_1 doi: 10.1080/2162402X.2014.1002723 – ident: e_1_2_7_12_1 doi: 10.1155/2015/248529 – ident: e_1_2_7_6_1 doi: 10.4161/onci.1.2.18481 – ident: e_1_2_7_35_1 doi: 10.1038/cmi.2010.11 – ident: e_1_2_7_33_1 doi: 10.1371/journal.pone.0062300 – ident: e_1_2_7_34_1 doi: 10.1016/j.intimp.2012.06.016 – volume: 20 start-page: 791 year: 2015 ident: e_1_2_7_2_1 article-title: Risk factors for recurrence in patients with resected N1 non‐small cell lung cancer—a systematic review and meta‐analysis publication-title: J Buon – ident: e_1_2_7_7_1 doi: 10.1007/s10555-015-9566-0 – ident: e_1_2_7_13_1 doi: 10.1074/jbc.M409024200 – ident: e_1_2_7_8_1 doi: 10.1038/srep10322 – ident: e_1_2_7_24_1 doi: 10.1016/j.ijrobp.2015.01.011 – ident: e_1_2_7_15_1 doi: 10.1016/j.canlet.2015.05.005 – ident: e_1_2_7_3_1 doi: 10.1097/JTO.0000000000000524 – ident: e_1_2_7_19_1 doi: 10.1155/2015/824746 – ident: e_1_2_7_21_1 doi: 10.1080/2162402X.2016.1249553 – ident: e_1_2_7_25_1 doi: 10.1615/CritRevImmunol.2015013607 – ident: e_1_2_7_9_1 doi: 10.1166/jbn.2015.2041 – ident: e_1_2_7_10_1 doi: 10.1016/j.cgh.2015.02.019 – ident: e_1_2_7_11_1 doi: 10.2174/1389201015666140813122703 – ident: e_1_2_7_29_1 doi: 10.1111/j.1600-065X.2008.00616.x – ident: e_1_2_7_31_1 doi: 10.1016/j.immuni.2015.05.016 – ident: e_1_2_7_28_1 doi: 10.1158/2326-6066.CIR-13-0138 – ident: e_1_2_7_16_1 doi: 10.1371/journal.pone.0112346 – ident: e_1_2_7_27_1 doi: 10.1038/srep10665 – ident: e_1_2_7_14_1 doi: 10.1371/journal.pone.0134110 – ident: e_1_2_7_30_1 doi: 10.4049/jimmunol.1202399 |
SSID | ssj0009932 |
Score | 2.5040014 |
Snippet | The regulatory T cells (Treg) play an important role in the tumor tolerance. The methods to regulate the Treg population in cancer‐bearing hosts are limited... The frequency of peripheral Treg in lung cancer patients was suppressed after treating with curcumin for 2 weeks. The peripheral Th1 cells were increased in... The regulatory T cells (Treg) play an important role in the tumor tolerance. The methods to regulate the Treg population in cancer-bearing hosts are limited... |
SourceID | proquest pubmed crossref wiley |
SourceType | Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 1420 |
SubjectTerms | Adult Aged Cancer Cell culture Curcumin Curcumin - administration & dosage Curcumin - pharmacology Cytometry Female Flow cytometry forkhead box protein‐3 Forkhead protein Forkhead Transcription Factors - genetics Forkhead Transcription Factors - metabolism Foxp3 protein Gene expression Humans Immunity Immunological tolerance Immunoregulation Interferon Interferon-gamma - metabolism Interferon‐γ Lung cancer Lung Neoplasms - drug therapy Lung Neoplasms - genetics Lung Neoplasms - immunology Lymphocytes Lymphocytes T Male Middle Aged Patients regulatory T cells T helper 1 cells T-Lymphocytes, Regulatory - cytology T-Lymphocytes, Regulatory - drug effects T-Lymphocytes, Regulatory - metabolism Th1 Cells - cytology Th1 Cells - drug effects Th1 Cells - metabolism Therapy Transcription Tumor Cells, Cultured |
Title | Curcumin converts Foxp3+ regulatory T cells to T helper 1 cells in patients with lung cancer |
URI | https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fjcb.26302 https://www.ncbi.nlm.nih.gov/pubmed/28731226 https://www.proquest.com/docview/1979769912 https://www.proquest.com/docview/1922503073 |
Volume | 119 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3NSx0xEB9EKPXSD631WSup9CDIPl82-0lP7aMiHnooCh6EJZNNsPV132M_DvrXd5LsrlhbkN7CbkKymcnML8nsbwA-8hQxFyq2_HY6iDJMAtRCBnEsyJuWFrG6ANlvyelFdHYZX67Bp-FfGM8PMR642ZXh7LVd4BKb43vS0J8Kp2EiHJGkjdWygOj7PXUU-V13g0AaHBCGCQdWoVl4PLZ86IseAcyHeNU5nJOXcDUM1ceZ3Ey7Fqfq7g8Wx__8llfwogei7LPXnNewpqtNeOZTU95uwvP5kAluC67mXa26Xz8q5mLU67Zh5LRW4ojVPpP9sr5l58zeATSsXVLxWi9Wuma8f0Yte_7WhtmDX7YgE8OUVbj6DVycfD2fnwZ9VoZACRJgICTXOJOl5qqUSvEyxCQXZSxMhhnmmJswo22OlCLNSyO5UTLiRpgk4mUelUpsw3q1rPQOsDRCNIlJY9pTRpmWGca5lNJgpDiGs2wCh4N8CtVTltvMGYvCky2HBU1c4SZuAgdj1ZXn6fhbpb1ByEW_VJuC5ylBMoLJ9PrD-Jpm2M6QrPSys3XI7DlzOIG3XjnGXmjLSeoVJjRYJ-J_d1-czb-4wu7Tq76DDYJomY8T34P1tu70e4JBLe47ff8No5YBbQ |
linkProvider | Wiley-Blackwell |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9QwEB5VrVC5UChQFgoYxAEJZbuO85R6KSuqpZQe0FbqARR5HFs8luwqmxzKr2dsJ6nKQ0LcrGQsO57xzOdHvgF4wVPEXKjY8tvpIMowCVALGcSxoGhaWsTqLsieJbPz6OQivtiAw_5fGM8PMWy42Znh_LWd4HZD-uCKNfSrwnGYCMskuWUzersF1Ycr8iiKvO4MgWw4IBQT9rxCk_BgqHo9Gv0GMa8jVhdyjnfgU99Zf9Pk27htcKx-_MLj-L9fcxtudViUHXnjuQMbutqFGz475eUubE_7ZHB34eO0rVX7_UvF3DX1ulkzilsr8YrVPpn9sr5kc2aPAdasWVLxs16sdM1494xqdhSua2b3ftmCvAxT1ubqe3B-_GY-nQVdYoZACdJhICTXOJGl5qqUSvEyxCQXZSxMhhnmmJswo5WOlCLNSyO5UTLiRpgk4mUelUrch81qWekHwNII0SQmjWlZGWVaZhjnUkqDkeIYTrIRvOwVVKiOtdwmz1gUnm85LGjgCjdwI3g-iK48VcefhPZ7LRfdbF0XPE8JlRFSptfPhtc0wnaEZKWXrZUhz-c84gj2vHUMrdCqk-wrTKizTsd_b744mb52hYf_LvoUtmfz96fF6duzd4_gJiG2zF8b34fNpm71Y0JFDT5xxv8TsqYFiA |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9QwEB5VrXhcCpTXlgIGcUBC2a5jJ3HECbasSkEVQq3UQ6XIdmzRss2ussmh_HrGdpKqPCTEzUrGsuMZz3x-5BuAVzRTKmc6cfx2JuJCpZEyTEZJwjCalg6x-guyh-n-MT84SU7W4G3_L0zghxg23NzM8P7aTfBlaXevSEPPtRrHKXNEkhs8nQhn0ntfr7ijMPD6IwQ04QhBTNzTCk3i3aHq9WD0G8K8Dlh9xJndgdO-r-Giyfdx26ix_vELjeN_fsxd2OyQKHkXTOcerJlqC26E3JSXW3Br2qeCuw-n07bW7cVZRfwl9bpZEYxaS_aG1CGV_aK-JEfEHQKsSLPA4jczX5qa0O4Z1uwIXFfE7fySOfoYop3F1Q_gePbhaLofdWkZIs1QgxGT1KiJLA3VpdSalrFKc1YmzAolVK5yGwtc50jJsry0klotObXMppyWOS81ewjr1aIyj4FkXCmb2izBRSUXRgqV5FJKq7imKp6IEbzu9VPojrPcpc6YF4FtOS5w4Ao_cCN4OYguA1HHn4R2eiUX3VxdFTTPEJMhTsbXL4bXOMJuhGRlFq2TQb_n_eEIHgXjGFrBNSeaV5xiZ72K_958cTB97wvb_y76HG5-2ZsVnz8efnoCtxGuiXBnfAfWm7o1TxESNeqZN_2fuoAEQA |
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=Curcumin+converts+Foxp3%2B+regulatory+T+cells+to+T+helper+1+cells+in+patients+with+lung+cancer&rft.jtitle=Journal+of+cellular+biochemistry&rft.au=Zou%2C+Jian+Y&rft.au=Su%2C+Chun+H&rft.au=Luo%2C+Hong+H&rft.au=Lei%2C+Yi+Y&rft.date=2018-02-01&rft.issn=1097-4644&rft.eissn=1097-4644&rft.volume=119&rft.issue=2&rft.spage=1420&rft_id=info:doi/10.1002%2Fjcb.26302&rft.externalDBID=NO_FULL_TEXT |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0730-2312&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0730-2312&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0730-2312&client=summon |