Chemosensitization of tumors by resveratrol

被引:249
作者
Gupta, Subash C. [1 ]
Kannappan, Ramaswamy [1 ]
Reuter, Simone [1 ]
Kim, Ji Hye [1 ]
Aggarwal, Bharat B. [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Expt Therapeut, Cytokine Res Lab, Houston, TX 77030 USA
来源
RESVERATROL AND HEALTH | 2011年 / 1215卷
基金
美国国家卫生研究院;
关键词
apoptosis; cancer therapy; chemoresistance; chemosensitization; resveratrol; tumor; FACTOR-KAPPA-B; PACLITAXEL-INDUCED APOPTOSIS; BREAST-CANCER-CELLS; MEDIATED MULTIDRUG-RESISTANCE; NEUROBLASTOMA SH-SY5Y CELL; DRUG-INDUCED APOPTOSIS; HUMAN OVARIAN-CANCER; P-GLYCOPROTEIN; DOWN-REGULATION; ANTICANCER AGENTS;
D O I
10.1111/j.1749-6632.2010.05852.x
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Because tumors develop resistance to chemotherapeutic agents, the cancer research community continues to search for effective chemosensitizers. One promising possibility is to use dietary agents that sensitize tumors to the chemotherapeutics. In this review, we discuss that the use of resveratrol can sensitize tumor cells to chemotherapeutic agents. The tumors shown to be sensitized by resveratrol include lung carcinoma, acute myeloid leukemia, promyelocytic leukemia, multiple myeloma, prostate cancer, oral epidermoid carcinoma, and pancreatic cancer. The chemotherapeutic agents include vincristine, adriamycin, paclitaxel, doxorubicin, cisplatin, gefitinib, 5-fluorouracil, velcade, and gemcitabine. The chemosensitization of tumor cells by resveratrol appears to be mediated through its ability to modulate multiple cell-signaling molecules, including drug transporters, cell survival proteins, cell proliferative proteins, and members of the NF-kappa B and STAT3 signaling pathways. Interestingly, this nutraceutical has also been reported to suppress apoptosis induced by paclitaxel, vincristine, and daunorubicin in some tumor cells. The potential mechanisms underlying this dual effect are discussed. Overall, studies suggest that resveratrol can be used to sensitize tumors to standard cancer chemotherapeutics.
引用
收藏
页码:150 / 160
页数:11
相关论文
共 72 条
[41]  
Lee JS, 1997, J CELL BIOCHEM, V65, P513, DOI 10.1002/(SICI)1097-4644(19970615)65:4<513::AID-JCB7>3.3.CO
[42]  
2-W
[43]  
LEE SC, 2005, CANC LETT, V288, P36
[44]   p53, the cellular gatekeeper for growth and division [J].
Levine, AJ .
CELL, 1997, 88 (03) :323-331
[45]   STATs: Transcriptional control and biological impact [J].
Levy, DE ;
Darnell, JE .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2002, 3 (09) :651-662
[46]   Human ovarian cancer and cisplatin resistance: Possible role of inhibitor of apoptosis proteins [J].
Li, JL ;
Feng, Q ;
Kim, JM ;
Schneiderman, D ;
Liston, P ;
Li, M ;
Vanderhyden, B ;
Faught, W ;
Fung, MFK ;
Senterman, M ;
Korneluk, RG ;
Tsang, BK .
ENDOCRINOLOGY, 2001, 142 (01) :370-380
[47]  
Liu L, 1999, CLIN CANCER RES, V5, P2908
[48]   c-FLIP inhibits chemotherapy-induced colorectal cancer cell death [J].
Longley, DB ;
Wilson, TR ;
McEwan, M ;
Allen, WL ;
McDermott, U ;
Galligan, L ;
Johnston, PG .
ONCOGENE, 2006, 25 (06) :838-848
[49]   Influence of epidermal growth factor receptor (EGFR), p53 and intrinsic MAP kinase pathway status of tumour cells on the antproliferative effect of ZD 1839 ('Iressa') [J].
Magné, N ;
Fischel, JL ;
Dubreuil, A ;
Formento, P ;
Poupon, MF ;
Laurent-Puig, P ;
Milano, G .
BRITISH JOURNAL OF CANCER, 2002, 86 (09) :1518-1523
[50]   Resveratrol confers resistance against taxol via induction of cell cycle arrest in human cancer cell lines [J].
Mao, Qi-Qi ;
Bai, Yu ;
Lin, Yi-Wei ;
Zheng, Xiang-Yi ;
Qin, Jie ;
Yang, Kai ;
Xie, Li-Ping .
MOLECULAR NUTRITION & FOOD RESEARCH, 2010, 54 (11) :1574-1584