The unfolded protein response as a target for cancer therapy

被引:97
|
作者
Nagelkerke, Anika [1 ,2 ]
Bussink, Johan [2 ]
Sweep, Fred C. G. J. [1 ]
Span, Paul N. [2 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Dept Lab Med, NL-6500 HB Nijmegen, Netherlands
[2] Radboud Univ Nijmegen, Med Ctr, Dept Radiat Oncol, NL-6500 HB Nijmegen, Netherlands
来源
关键词
Unfolded protein response; Cancer; Therapy; Endoplasmic reticulum stress; Autophagy; ENDOPLASMIC-RETICULUM STRESS; ACTIVATING TRANSCRIPTION FACTOR-4; GLUCOSE-REGULATED STRESSES; LYMPH-NODE METASTASIS; ER STRESS; BREAST-CANCER; INDUCED AUTOPHAGY; MESSENGER-RNA; CELL-SURVIVAL; CHAPERONE GRP78/BIP;
D O I
10.1016/j.bbcan.2014.07.006
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
Various physiological and pathological conditions generate an accumulation of misfolded proteins in the endoplasmic reticulum (ER). This results in ER stress followed by a cellular response to cope with this stress and restore homeostasis: the unfolded protein response (UPR). Overall, the UPR leads to general translational arrest and the induction of specific factors to ensure cell survival or to mediate cell death if the stress is too severe. In multiple cancers, components of the UPR are overexpressed, indicating increased dependence on the UPR. In addition, the UPR can confer resistance to anti-cancer treatment. Therefore, modification of the UPR should be explored for its anti-cancer properties. This review discusses factors associated with the UPR that represent potential therapeutic targets. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:277 / 284
页数:8
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