Cell death decision by p53 via control of the mitochondrial membrane

被引：89

作者：

Dashzeveg, Nurmaa ^{[1
]}

Yoshida, Kiyotsugu ^{[1
]}

机构：

[1] Jikei Univ, Sch Med, Dept Biochem, Minato Ku, Tokyo 1058461, Japan

来源：

CANCER LETTERS | 2015年 / 367卷 / 02期

基金：

日本学术振兴会;

关键词：

p53; Mitochondria; Apoptosis; Necrosis; Necroptosis; TUMOR-SUPPRESSOR P53; DNA-BINDING DOMAIN; BCL-2; FAMILY; MULTIDRUG-RESISTANCE; TARGETING BCL2; IN-VITRO; BAX; APOPTOSIS; NECROSIS; PUMA;

D O I：

10.1016/j.canlet.2015.07.019

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

The tumor suppressor p53 is mutated in more than half of human cancers. Recent evidence has revealed that p53 not only regulates apoptosis but also regulates necrotic/necroptotic cell death via the mitochondria. The regulation of apoptosis by p53 is tightly connected to the mitochondrial outer membrane permeabilization and the induction of and interaction with Bcl-2 family members. Interestingly, p53-mediated regulation of necrosis/necroptosis is correlated with mitochondrial permeabilization pore opening via interactions with CypD and Drp1. This review discusses the p53-regulating molecules that induce apoptosis or necrosis/necroptosis via the mitochondria. (C) 2015 Elsevier Ireland Ltd. All rights reserved.

引用

页码：108 / 112

页数：5

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