EGCG synergizes the therapeutic effect of cisplatin and oxaliplatin through autophagic pathway in human colorectal cancer cells

被引:89
作者
Hu, Fen [1 ]
Wei, Fei [2 ]
Wang, Yulei [1 ]
Wu, Bibo [1 ]
Fang, Yuan [1 ]
Xiong, Bin [1 ]
机构
[1] Wuhan Univ, Zhongnan Hosp, Hubei Canc Clin Study Ctr, Dept Oncol,Hubei Key Lab Tumor Biol Behav, Wuhan 430071, Peoples R China
[2] Wuhan Univ, Sch Med, Res Ctr Food & Drug Evaluat,State Key Lab Virol, Inst Med Virol,Natl Lab Antiviral & Tumor Traditi, Wuhan 430071, Peoples R China
基金
国家高技术研究发展计划(863计划);
关键词
EGCG; Cisplatin; Oxaliplatin; Autophagic death; GREEN TEA POLYPHENOL; EPIGALLOCATECHIN GALLATE; PROSTATE-CANCER; COLON-CANCER; APOPTOSIS; DEATH; CHEMOTHERAPY; SUPEROXIDE; INHIBITORS;
D O I
10.1016/j.jphs.2015.04.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Application of the platinum-based chemotherapy for colorectal cancer is restricted due to its severe cytotoxic effects. In this study we used synergistic strategies by combining (-)-Epigallocatechin gallate (EGCG) with cisplatin or oxaliplatin to minimize the ill effects of platinum-based therapy. MTS assay was used to examine the effect of EGCG, cisplatin and oxaliplatin on the proliferation of human colorectal cancer DLD-1 and HT-29 cells. Autophagic process was evaluated by detection of LC3-II protein, auto-phagosome formation, and quantification of Acidic Vesicular. Treatment of DLD-1 and HT-29 cells with EGCG plus cisplatin or oxaliplatin showed a synergistic effect on inhibition of cell proliferation and induction of cell death. EGCG enhanced the effect of cisplatin and oxaliplatin-induced autophagy in DLD-1 and HT-29 cells, as characterized by the accumulation of LC3-II protein, the increase of acidic vesicular organelles (AVOs), and the formation of autophagosome. In addition, transfection of DLD-1 and HT-29 cells with siRNA against ATG genes reduced EGCG synergistic effect. Our findings suggest that combining EGCG with cisplatin or oxaliplatin could potentiate the cytotoxicity of cisplatin and oxaliplatin in colorectal cancer cells through autophagy related pathway. (C) 2015 Production and hosting by Elsevier B.V. on behalf of Japanese Pharmacological Society.
引用
收藏
页码:27 / 34
页数:8
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