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Transcription-independent p53 apoptosis: an alternative route to death
被引:324
作者:

Speidel, Daniel
论文数: 0 引用数: 0
h-index: 0
机构:
Childrens Med Res Inst, Cell Transformat Unit, Westmead, NSW 2145, Australia Childrens Med Res Inst, Cell Transformat Unit, Westmead, NSW 2145, Australia
机构:
[1] Childrens Med Res Inst, Cell Transformat Unit, Westmead, NSW 2145, Australia
关键词:
WILD-TYPE P53;
DNA-BINDING DOMAIN;
COLORECTAL-CANCER CELLS;
TUMOR-SUPPRESSOR P53;
MITOCHONDRIAL P53;
P53-DEPENDENT APOPTOSIS;
P53-MEDIATED APOPTOSIS;
IN-VIVO;
MUTANT P53;
CYTOPLASMIC SEQUESTRATION;
D O I:
10.1016/j.tcb.2009.10.002
中图分类号:
Q2 [细胞生物学];
学科分类号:
071013 [干细胞生物学];
摘要:
Apoptosis induced by p53 is firmly established as a central mechanism of tumour suppression. In addition to its complex functions as a nuclear transcription factor, p53 can act in the cytosol and mitochondria to promote apoptosis through transcription-independent mechanisms. Recent studies have shown that physical and functional interactions of p53 with various members of the Bcl-2 family provide the basis for this alternative route of p53-mediated cell death. However, different models of how these interactions promote apoptosis have been proposed. This review focuses on the mechanisms, regulation and physiological roles of transcription-independent p53 activities and highlights recent findings suggesting that the utilisation of these activities provides a promising alternative strategy for p53-based cancer therapy.
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页码:14 / 24
页数:11
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