Micromanagement of the mitochondrial apoptotic pathway by p53

被引:19
|
作者
Walia, Vijay [1 ,2 ]
Kakar, Smita [3 ]
Elble, Randolph [1 ,2 ]
机构
[1] So Illinois Univ, Sch Med, Dept Pharmacol, Springfield, IL 62794 USA
[2] So Illinois Univ, Sch Med, Simmons Canc Inst, Springfield, IL 62794 USA
[3] Iowa State Univ, Dept Biochem Biophys & Mol Biol, Ames, IA 50011 USA
来源
关键词
Mitochondria; p53; Nontranscriptional; Apoptosis; Interaction; Bcl-2; family; CLIC4; Review; CHLORIDE CHANNEL PROTEIN; DNA-BINDING DOMAIN; STRESS-INDUCED P53; BCL-X-L; P53-DEPENDENT APOPTOSIS; MOLECULAR-CLONING; BREAST-CANCER; CELL-DEATH; BAX; TRANSLOCATION;
D O I
10.2741/3717
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
It is now well established that p53 is the primary arbiter of stress-response and the principal barrier to neoplastic processes at the cellular level. Perhaps the most potent weapon in p53's tumor suppressive arsenal is apoptosis, enacted as a last resort when all other remedies are exhausted. Initially, the mechanism was thought to be simply activation or repression of Bcl-2 family members by p53. More recently, evidence of a more rapid pathway emerged whereby p53 physically interacts with Bcl-2 family members to tip the balance toward apoptosis. This review details the multiple levels of regulation of mitochondrially-directed apoptosis by p53, including recent findings of how p53 translocation is regulated.
引用
收藏
页码:749 / 758
页数:10
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