Resveratrol Induces Cell-Cycle Disruption and Apoptosis in Chemoresistant B16 Melanoma

被引:97
作者
Gatouillat, Gregory [1 ]
Balasse, Emilie [1 ]
Joseph-Pietras, Debora [2 ]
Morjani, Hamid [1 ,3 ]
Madoulet, Claudie [1 ]
机构
[1] URCA, Dept Biochem & Mol Biol, Fac Pharm, F-51096 Reims, France
[2] Univ Southampton, Sch Med, Canc Sci Div, Southampton, Hants, England
[3] URCA, CNRS, Fac Pharm, MEDyC,UMR6237, F-51096 Reims, France
关键词
RESVERATROL; CHEMORESISTANT MELANOMA; CELL CYCLE; APOPTOSIS; CHEMOPREVENTION; METASTATIC MALIGNANT-MELANOMA; CANCER-CELLS; TUMOR-GROWTH; UP-REGULATION; IN-VIVO; MULTIDRUG-RESISTANCE; P-GLYCOPROTEIN; RED WINE; KAPPA-B; ARREST;
D O I
10.1002/jcb.22601
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Resveratrol, a naturally occurring polyphenol, has been shown to possess chemopreventive activities. In this study, we show that resveratrol (0-500 mu M) inhibits the growth of a doxorubicin-resistant B16 melanoma cell subtitle (B16/DOX) (IC50 = 25 mu M after 72 h, P < 0.05). This was accomplished by imposing an artificial checkpoint at the G(1)-S phase transition, as demonstrated by cell-cycle analysis and down-regulation of cyclin D1/cdk4 anti increased of p53 expression level. The G(1)-phase arrest of cell cycle in resveratrol-treated (10-100 mu M) B16/DOX cells was followed by the induction of apoptosis, which was revealed by pyknotic nuclei and fragmented DNA. Resveratrol also potentiated at subtoxic dose (25 mu M for 24 h) doxorubicin cytotoxicity in the chemoresistant B16 melanoma (P<0.01). When administered to mice, resveratrol (12.5 mg/kg) reduced the growth of an established B16/DOX melanoma and prolonged survival (32% compared to untreated mice). All these data support a potential use of resveratrol alone or in combination with other chemotherapeutic agents in the management of chemoresistant tumors. J. Cell. Biochem. 110: 893-902, 2010. (C) 2010 Wiley-Liss. Inc.
引用
收藏
页码:893 / 902
页数:10
相关论文
共 60 条
[1]  
Ahmad N, 2001, CLIN CANCER RES, V7, P1466
[2]   Resveratrol as an antioxidant and pro-oxidant agent: mechanisms and clinical implications [J].
Alarcn de la Lastral, C. ;
Villegas, I. .
BIOCHEMICAL SOCIETY TRANSACTIONS, 2007, 35 :1156-1160
[3]   Inhibition of cancer growth by resveratrol is related to its low bioavailability [J].
Asensi, M ;
Medina, I ;
Ortega, A ;
Carretero, J ;
Baño, MC ;
Obrador, E ;
Estrela, JM .
FREE RADICAL BIOLOGY AND MEDICINE, 2002, 33 (03) :387-398
[4]   Multiple molecular targets of resveratrol: Anti-carcinogenic mechanisms [J].
Athar, Mohammad ;
Back, Jung Ho ;
Kopelovich, Levy ;
Bickers, David R. ;
Kim, Arianna L. .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2009, 486 (02) :95-102
[5]   Living with p53, dying of p53 [J].
Aylon, Yael ;
Oren, Moshe .
CELL, 2007, 130 (04) :597-600
[6]  
Bader Y, 2008, ONCOL REP, V19, P801
[7]   αvβ3 Integrin-dependent antiangiogenic activity of resveratrol stereoisomers [J].
Belleri, Mirella ;
Ribatti, Domenico ;
Savio, Monica ;
Stivala, Lucia Anna ;
Forti, Luca ;
Tanghetti, Elena ;
Alessi, Patrizia ;
Coltrini, Daniela ;
Bugatti, Antonella ;
Mitola, Stefania ;
Nicoli, Stefanie ;
Vannini, Vanio ;
Presta, Marco .
MOLECULAR CANCER THERAPEUTICS, 2008, 7 (12) :3761-3770
[8]   Mechanisms involved in resveratrol-induced apoptosis and cell cycle arrest in prostate cancer-derived cell lines [J].
Benitez, Dixan A. ;
Pozo-Guisado, Eulalia ;
Alvarez-Barrientos, Alberto ;
Fernandez-Salguero, Pedro M. ;
Castellon, Enrique A. .
JOURNAL OF ANDROLOGY, 2007, 28 (02) :282-293
[9]   Resveratrol inhibits proliferation, induces apoptosis, and overcomes chemoresistance through down-regulation of STAT3 and nuclear factor-κB-regulated antiapoptotic and cell survival gene products in human multiple myeloma cells [J].
Bhardwaj, Anjana ;
Sethi, Gautam ;
Vadhan-Raj, Saroj ;
Bueso-Ramos, Carlos ;
Takada, Yasunari ;
Gaur, Upasna ;
Nair, Asha S. ;
Shishodia, Shishir ;
Aggarwal, Bharat B. .
BLOOD, 2007, 109 (06) :2293-2302
[10]   DNA repair pathways in drug resistance in melanoma [J].
Bradbury, PA ;
Middleton, MR .
ANTI-CANCER DRUGS, 2004, 15 (05) :421-426