共 61 条
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.
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页码:414 / 420
页数:7
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