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...

Full description

Saved in:
Bibliographic Details
Published inJournal of cellular biochemistry Vol. 119; no. 2; pp. 1420 - 1428
Main Authors Zou, Jian Y., Su, Chun H., Luo, Hong H., Lei, Yi Y., Zeng, Bo, Zhu, Hao S., Chen, Zhen G.
Format Journal Article
LanguageEnglish
Published United States Wiley Subscription Services, Inc 01.02.2018
Subjects
Online AccessGet 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