The mitochondrial p53 pathway

被引:493
作者
Vaseva, Angelina V. [1 ]
Moll, Ute M. [1 ]
机构
[1] SUNY Stony Brook, Dept Pathol, Stony Brook, NY 11794 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS | 2009年 / 1787卷 / 05期
关键词
p53; Mitochondria; Apoptosis; Transcription; Bcl-2; family; Pathophysiology; Radiosensitivity; Ischemia; GLOBAL CEREBRAL-ISCHEMIA; DNA-BINDING DOMAIN; IN-VIVO; GENE-THERAPY; CELL-DEATH; MEMBRANE PERMEABILIZATION; P53-DEPENDENT APOPTOSIS; TRANSCRIPTION FACTORS; TUMOR-SUPPRESSOR; GTP DEPLETION;
D O I
10.1016/j.bbabio.2008.10.005
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
p53 is one of the most mutated tumor suppressors in human cancers and as such has been intensively studied for a long time. p53 is a major orchestrator of the cellular response to a broad array of stress types by regulating apoptosis, cell cycle arrest, senescence, DNA repair and genetic stability. For a long time it was thought that these functions of p53 solely rely on its function as a transcription factor, and numerous p53 target genes have been identified [1]. In the last 8 years however, a novel transcription-independent proapoptotic function mediated by the cytoplasmic pool of p53 has been revealed. p53 participates directly in the intrinsic apoptosis pathway by interacting with the multidomain members of the Bcl-2 family to induce mitochondrial outer membrane permeabilization. Our review will discuss these studies, focusing on recent advances in the field. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:414 / 420
页数:7
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