Endoplasmic reticulum stress associated responses in cancer

被引:227
作者
Wang, Wen-An [1 ]
Groenendyk, Jody [1 ]
Michalak, Marek [1 ]
机构
[1] Univ Alberta, Dept Biochem, Edmonton, AB T6G 2H7, Canada
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2014年 / 1843卷 / 10期
关键词
Endoplasmic reticulum stress; Cancer; Unfolded protein response; UNFOLDED-PROTEIN RESPONSE; PLASMA-CELL DIFFERENTIATION; XBP1; MESSENGER-RNA; ER STRESS; TRANSCRIPTION FACTOR; MULTIPLE-MYELOMA; SMALL-MOLECULE; TUMOR-GROWTH; HEPATOCELLULAR-CARCINOMA; TRANSLATIONAL REGULATION;
D O I
10.1016/j.bbamcr.2014.01.012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The endoplasmic reticulum (ER) is responsible for many housekeeping functions within the cell and is an important site for pathways that regulates its state of homeostasis. When cellular states perturb ER functions, a phenomenon termed "ER stress" activates a number of pathways to counteract the associated damages; these pathways are together called the unfolded protein response (UPR). The UPR has a dualistic function; it exists to alleviate damage associated with ER stress, however, if this is not possible, then it signals for cell death through apoptosis. Cancer cells are shown to be very resilient under extreme environmental stress and an increasing number of studies have indicated that this may be largely due to an altered state of the UPR. The role of ER stress and the UPR in cancer is still not clear, however many components are involved and may prove to be promising targets in future anti-cancer therapy. This article is part of a Special Issue entitled: Calcium Signaling in Health and Disease. Guest Editors: Geert Bultynck, Jacques Haiech, Claus W. Heizmann, Joachim Krebs, and Marc Moreau. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:2143 / 2149
页数:7
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