Targeting autophagy potentiates chemotherapy-induced apoptosis and proliferation inhibition in hepatocarcinoma cells

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• 作者：Xian-ling Guo^a ; ^b ; ¹ ; Ding Li^a ; ¹ ; Fei Hu^a ; ¹ ; Jian-rui Song^a ; Shan-shan Zhang^a ; Wei-jie Deng^a ; Kai Sun^a ; Qiu-dong Zhao^a ; Xu-qin Xie^a ; Yu-jiao Song^a ; Meng-chao Wu^a ; Li-xin Wei^a ; ^{weilixin@yahoo.com}
• 关键词：Autophagy ; Hepatocarcinoma ; Chemotherapy ; Apoptosis ; Proliferation
• 刊名：Cancer Letters
• 出版年：2012
• 期刊代码：44_03043835
• 类别：med
• 出版时间：28 July, 2012
• 卷：320
• 期：2
• 页码：171-179
• 文件大小：1706 K

摘要

Induction of cell death and inhibition of cell growth are the main targets of cancer therapy. Here we evaluated the role of autophagy on chemoresistance of human hepatocarcinoma (HCC) cell lines, focusing on its crosstalk with cell apoptosis and proliferation. In this study, a chemotherapeutic agent (cisplatin or 5FU) induced the formation of autophagosomes in three human HCC cell lines and upregulated the expression of autophagy protein LC3-II. Inhibition of autophagy by 3-methyladenine or si-beclin 1 increased chemotherapy-induced apoptosis in HCC cells. Meanwhile, increased damage of the mitochondrial membrane potential was also observed in HCC cells when autophagy was inhibited. Furthermore, inhibition of autophagy reduced clone formation and impaired cell growth of HCC cells when treated with chemotherapy. Co-administration of an autophagy inhibitor (chloroquine) and chemotherapy significantly inhibited tumor growth in a mouse xenograft tumor model, with greater extent of apoptosis and impaired proliferation of tumor cells. This study suggests that autophagy is a potential novel target to improve therapy efficiency of conventional chemotherapeutics towards HCC.