Cytoprotective small molecule modulators of endoplasmic reticulum stress

被引:4
|
作者
Munshi, Soumyabrata [1 ]
Dahl, Russell [2 ]
机构
[1] Rosalind Franklin Univ Med & Sci, Dept Neurosci, 3333 Green Bay Rd, N Chicago, IL 60064 USA
[2] Neurodon LLC, 5700 Tanager St, Schererville, IN 46375 USA
关键词
ER stress; Endoplasmic reticulum; Drug discovery; Small molecules; Medicinal chemistry; UNFOLDED PROTEIN RESPONSE; XBP1; MESSENGER-RNA; ER-STRESS; MULTIPLE-MYELOMA; INFLAMMATORY RESPONSE; TRANSCRIPTION FACTOR; HUMAN-DISEASE; PC12; CELLS; BETA-CELLS; INHIBITION;
D O I
10.1016/j.bmc.2016.03.045
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
Cellular health depends on the normal function of the endoplasmic reticulum ( ER) to fold, assemble, and modify critical proteins to maintain viability. When the ER cannot process proteins effectively, a condition known as ER stress ensues. When this stress is excessive or prolonged, cell death via apoptotic pathways is triggered. Interestingly, most major diseases have been shown to be intimately linked to ER stress, including diabetes, stroke, neurodegeneration, and many cancers. Thus, controlling ER stress presents a significant strategy for drug development for these diseases. The goal of this review is to present various small molecules that alleviate ER stress with the intention that they may serve as useful starting points for therapeutic agent development. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2382 / 2388
页数:7
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