A role for peroxisome proliferator-activated receptor gamma in resveratrol-induced colon cancer cell apoptosis

被引:42
作者
Aires, Virginie [1 ,2 ]
Brassart, Bertrand [3 ]
Carlier, Annie [3 ]
Scagliarini, Alessandra [1 ,2 ]
Mandard, Stephane [1 ,4 ]
Limagne, Emeric [1 ,2 ]
Solary, Eric [5 ]
Martiny, Laurent [3 ]
Tarpin, Michel [3 ]
Delmas, Dominique [1 ,2 ]
机构
[1] Univ Bourgogne, Dijon, France
[2] INSERM, Ctr Rech, U866, Equipe Chimiotherapie Metab Lipid & Reponse Immun, Dijon, France
[3] Univ Reims, Fac Sci Exactes & Nat, Reims, France
[4] INSERM, U866, Ctr Rech, Equipe Prot Transfert Lipides & Metab Lipoprot, Dijon, France
[5] Inst Gustave Roussy, INSERM, UMR 1009, Villejuif, France
关键词
Apoptosis; Cell proliferation; Colon cancer; Polyphenols; PPAR; Resveratrol; PPAR-GAMMA; CYCLE PROGRESSION; GROWTH; CHEMOPREVENTION; RAFTS; REDISTRIBUTION; EXPRESSION; CARCINOMA; PATHWAYS; LIGANDS;
D O I
10.1002/mnfr.201300962
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Scope: Resveratrol may function as a chemopreventive agent. A recent clinical study demonstrates a reduction in tumor cell proliferation in colorectal patients receiving repeated oral ingestion of resveratrol. However, gaps remain in our knowledge of the molecular mechanisms by which resveratrol exerts its chemopreventive effect. We have previously demonstrated that resveratrol induces apoptosis in colon cancer cells and that resveratrol can sensitize chemoresistant colon cancer cells to various drugs. Based on its ability to activate peroxisome proliferator-activated receptor gamma (PPAR gamma) in colon cancer cells, we sought to determine the implication of this nuclear transcription factor in resveratrol-induced apoptosis. Methods and results: Transient transfection of cancer cells with a dominant-negative PPAR gamma mutant or treatment with a PPAR gamma antagonist (GW9662) reversed the inhibitory effect of resveratrol. Moreover, GW9662 prevented disruption of the cell cycle induced by resveratrol and consequently abrogated resveratrol-induced apoptosis. Tumor cell death was potentiated by combining resveratrol with rosiglitazone, a PPAR gamma agonist. Conclusion: The results show that PPAR gamma plays a role in resveratrol-induced apoptosis of colon carcinoma cells. The combination of resveratrol with a PPAR gamma agonist could be a promising pharmacological approach for treatment of colorectal cancer.
引用
收藏
页码:1785 / 1794
页数:10
相关论文
共 43 条
[31]   The role of peroxisome proliferator-activated receptors in carcinogenesis and chemoprevention [J].
Peters, Jeffrey M. ;
Shah, Yatrik M. ;
Gonzalez, Frank J. .
NATURE REVIEWS CANCER, 2012, 12 (03) :181-195
[32]   Alcohol and mortality in middle-aged men from Eastern France [J].
Renaud, SC ;
Guéguen, R ;
Schenker, J ;
d'Houtaud, A .
EPIDEMIOLOGY, 1998, 9 (02) :184-188
[33]   Peroxisome proliferator-activated receptors in tumorigenesis: Targets of tumour promotion and treatment [J].
Roberts-Thomson, SJ .
IMMUNOLOGY AND CELL BIOLOGY, 2000, 78 (04) :436-441
[34]   Differentiation and reversal of malignant changes in colon cancer through PPARγ [J].
Sarraf, P ;
Mueller, E ;
Jones, D ;
King, FJ ;
DeAngelo, DJ ;
Partridge, JB ;
Holden, SA ;
Chen, LB ;
Singer, S ;
Fletcher, C ;
Spiegelman, BM .
NATURE MEDICINE, 1998, 4 (09) :1046-1052
[35]   GW9662, a potent antagonist of PPARγ, inhibits growth of breast tumour cells and promotes the anticancer effects of the PPARγ agonist rosiglitazone, independently of PPARγ activation [J].
Seargent, JM ;
Yates, EA ;
Gill, JH .
BRITISH JOURNAL OF PHARMACOLOGY, 2004, 143 (08) :933-937
[36]  
Shih A, 2004, MOL CANCER THER, V3, P1355
[37]   Green tea, black tea and breast cancer risk: a meta-analysis of epidemiological studies [J].
Sun, Can-Lan ;
Yuan, Jian-Min ;
Koh, Woon-Puay ;
Yu, Mimi C. .
CARCINOGENESIS, 2006, 27 (07) :1310-1315
[38]   Cancer chemoprevention with dietary phytochemicals [J].
Surh, YJ .
NATURE REVIEWS CANCER, 2003, 3 (10) :768-780
[39]   Resveratrol depresses the growth of colorectal aberrant crypt foci by affecting bax and p21CIP expression [J].
Tessitore, L ;
Davit, A ;
Sarotto, I ;
Caderni, G .
CARCINOGENESIS, 2000, 21 (08) :1619-1622
[40]   Peroxisome proliferator-activated receptor γ as a molecular target of resveratrol-induced modulation of polyamine metabolism [J].
Ulrich, Sandra ;
Loitsch, Stefan M. ;
Rau, Oliver ;
von Knethen, Andreas ;
Bruene, Bernhard ;
Schubert-Zsilavecz, Manfred ;
Stein, Juergen M. .
CANCER RESEARCH, 2006, 66 (14) :7348-7354