Inhibition of autophagy enhances apoptosis induced by the PI3K/AKT/mTor inhibitor NVP-BEZ235 in renal cell carcinoma cells

被引:61
作者
Li, Hongyan [1 ]
Jin, Xuefei [1 ]
Zhang, Zhuo [1 ]
Xing, Yuanyuan [1 ]
Kong, Xiangbo [1 ]
机构
[1] Jilin Univ, China Japan Union Hosp, Dept Urol, Changchun 130033, Jilin, Peoples R China
关键词
BEZ235; AKT; autophagy; apoptosis; renal cell carcinoma; PHOSPHATIDYLINOSITOL 3-KINASE/MAMMALIAN TARGET; DUAL PI3K/MTOR INHIBITOR; MTOR INHIBITION; RAPAMYCIN INHIBITOR; CANCER; TUMOR; DEATH; COMBINATION; THERAPY; PATHWAY;
D O I
10.1002/cbf.2917
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
The PI3K/AKT/mTOR pathway plays a key role in the development of the hypervascular tumor renal cell carcinoma (RCC). NVP-BEZ235 (NVP), a novel dual PI3K/mTOR inhibitor, showed great antitumor benefit and provided a treatment strategy in RCC. In this study, we test the effect of NVP on survival rate, apoptosis and autophagy in the RCC cell line, 786-0. We also explore the hypothesis that NVP, in combination with autophagy inhibitors, leads to apoptosis enhancement in 786-0 cells. The results showed that the PI3K/AKT/mTOR pathway proteins p-AKT and p-P70S6K were highly expressed in RCC tissue. We also showed that NVP inhibited cell growth and induced apoptosis and autophagy in RCC cells. The combination treatment of NVP with autophagy inhibitors enhanced the effect of NVP on suppressing 786-0 growth and induction of apoptosis. This study proposes a novel treatment paradigm where combining PI3K/AKT/mTOR pathway inhibitors and autophagy inhibitors lead to enhanced RCC cell apoptosis. Copyright (c) 2012 John Wiley & Sons, Ltd.
引用
收藏
页码:427 / 433
页数:7
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