自噬
内质网
细胞凋亡
未折叠蛋白反应
程序性细胞死亡
细胞生物学
体外
化学
线粒体
癌症研究
生物
生物化学
作者
Jian‐Jiang Zhong,Ye Xu,Yi Hu,Jing Su,Huimei Yu,Xiyan Xiang,Xiaoning Li,Zhichao Zhang,Liankun Sun
出处
期刊:Cancer Letters
[Elsevier]
日期:2012-10-01
卷期号:323 (2): 180-187
被引量:49
标识
DOI:10.1016/j.canlet.2012.04.009
摘要
Previous results showed that a novel BH3 mimetic S1 could induce cell death in a wide range of cancer types in vitro through Bax/Bak-dependent apoptosis. We demonstrated that in addition to mitochondrial pathway apoptosis, endoplasmic reticulum (ER) stress-associated apoptosis was also induced by S1. Moreover, S1 can induce autophagy in U251 cells, which may occur through ER stress and disruption of the association of Bcl-2 and Beclin 1. Inhibition of autophagy by the autophagic inhibitors 3-methyladenine (3-MA) or chloroquine (CQ) increased S1-induced apoptosis. In conclusion, autophagy plays an important role in S1-induced U251 cell death.
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