Coordination of Autophagy and the Proteasome in Resolving Endoplasmic Reticulum Stress

被引:24
作者
Chen, X. [1 ]
Yin, X. -M. [1 ]
机构
[1] Indiana Univ Sch Med, Dept Pathol & Lab Med, Indianapolis, IN 46202 USA
基金
美国国家卫生研究院;
关键词
autophagy; proteasome; endoplasmic reticulum stress; apoptosis; anticancer; UNFOLDED PROTEIN RESPONSE; CELL-SURVIVAL; ER STRESS; DEGRADATION; DEATH; INHIBITORS; APOPTOSIS; SYSTEM; FUSION; BCL-2;
D O I
10.1177/0300985810385154
中图分类号
R36 [病理学];
学科分类号
100103 [病原生物学];
摘要
Macroautophagy is a cellular degradation mechanism that involves the delivery of cytosolic components (macromolecules or organelles) by the autophagosome to the lysosome for degradation. In mammalian cells, macroautophagy and the ubiquitin proteasome system are 2 major mechanisms to eliminate abnormal proteins accumulated in pathological conditions. Here, the coordination of the 2 pathways to alleviate endoplasmic reticulum stress is reviewed. Also discussed is the regulatory role of macroautophagy and proteasome activity in cell survival and death, as well as the recent discoveries leading to novel strategies of simultaneous control of the proteasome and autophagy activity in anticancer treatment.
引用
收藏
页码:245 / 253
页数:9
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