Structural biology of the tumor suppressor p53 and cancer-associated mutants

被引:82
作者
Joerger, Andreas C. [1 ]
Fersht, Alan R. [1 ]
机构
[1] MRC, Ctr Prot Engn, Cambridge CB2 2QH, England
来源
ADVANCES IN CANCER RESEARCH, VOL 97 | 2007年 / 97卷
基金
英国医学研究理事会;
关键词
D O I
10.1016/S0065-230X(06)97001-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The tumor suppressor protein p53 is a transcription factor that plays a key role in the prevention of cancer development. In response to oncogenic or other stresses, the p53 protein is activated and regulates the expression of a variety of target genes, resulting in cell cycle arrest, senescence, or apoptosis. Mutation of the p53 gene is the most common genetic alteration in human cancer, affecting more than 50% of human tumors. Most of these mutations inactivate the DNA-binding domain of the protein. In this chapter, we describe the structure of the wild-type p53 protein and present structural and functional data that provide the molecular basis for understanding the effects of common cancer mutations. Further, we assess novel therapeutic strategies that aim to rescue the function of p53 cancer mutants. (c) 2007 Elsevier Inc.
引用
收藏
页码:1 / +
页数:26
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