Mitochondrial apoptosis: killing cancer using the enemy within

被引:636
作者
Lopez, J. [1 ]
Tait, S. W. G. [1 ]
机构
[1] Univ Glasgow, Inst Canc Sci, Canc Res UK Beatson Inst, Glasgow G61 1BD, Lanark, Scotland
基金
英国生物技术与生命科学研究理事会;
关键词
apoptosis; mitochondria; BCL-2; cancer therapy; CHRONIC LYMPHOCYTIC-LEUKEMIA; CYTOCHROME-C RELEASE; BCL-2; FAMILY; CELL-DEATH; RESISTANCE; PROTEINS; ABT-737; MCL-1; INHIBITOR; SURVIVAL;
D O I
10.1038/bjc.2015.85
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Apoptotic cell death inhibits oncogenesis at multiple stages, ranging from transformation to metastasis. Consequently, in order for cancer to develop and progress, apoptosis must be inhibited. Cell death also plays major roles in cancer treatment, serving as the main effector function of many anti-cancer therapies. In this review, we discuss the role of apoptosis in the development and treatment of cancer. Specifically, we focus upon the mitochondrial pathway of apoptosis-the most commonly deregulated form of cell death in cancer. In this process, mitochondrial outer membrane permeabilisation or MOMP represents the defining event that irrevocably commits a cell to die. We provide an overview of how this pathway is regulated by BCL-2 family proteins and describe ways in which cancer cells can block it. Finally, we discuss exciting new approaches aimed at specifically inducing mitochondrial apoptosis in cancer cells, outlining their potential pitfalls, while highlighting their considerable therapeutic promise.
引用
收藏
页码:957 / 962
页数:6
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