Micromanagement of the mitochondrial apoptotic pathway by p53
被引:19
|
作者:
Walia, Vijay
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机构:
So Illinois Univ, Sch Med, Dept Pharmacol, Springfield, IL 62794 USA
So Illinois Univ, Sch Med, Simmons Canc Inst, Springfield, IL 62794 USASo Illinois Univ, Sch Med, Dept Pharmacol, Springfield, IL 62794 USA
Walia, Vijay
[1
,2
]
Kakar, Smita
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机构:
Iowa State Univ, Dept Biochem Biophys & Mol Biol, Ames, IA 50011 USASo Illinois Univ, Sch Med, Dept Pharmacol, Springfield, IL 62794 USA
Kakar, Smita
[3
]
Elble, Randolph
论文数: 0引用数: 0
h-index: 0
机构:
So Illinois Univ, Sch Med, Dept Pharmacol, Springfield, IL 62794 USA
So Illinois Univ, Sch Med, Simmons Canc Inst, Springfield, IL 62794 USASo Illinois Univ, Sch Med, Dept Pharmacol, Springfield, IL 62794 USA
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
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.