Mouse Models of p53 Functions

被引:65
作者
Lozano, Guillermina [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Genet, Houston, TX 77030 USA
关键词
RADIATION-INDUCED APOPTOSIS; WILD-TYPE P53; EMBRYONIC LETHALITY; DNA-DAMAGE; CELL-DEATH; P53-DEPENDENT APOPTOSIS; MDM2-DEFICIENT MICE; NERVOUS-SYSTEM; POINT MUTATION; MUTANT P53;
D O I
10.1101/cshperspect.a001115
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Studies in mice have yielded invaluable insight into our understanding of the p53 pathway. Mouse models with activated p53, no p53, and mutant p53 have queried the role of p53 in development and tumorigenesis. In these models, p53 is activated and stabilized via redundant posttranslational modifications. On activation, p53 initiates two major responses: inhibition of proliferation (via cell-cycle arrest, quiescence, senescence, and differentiation) and induction of apoptosis. Importantly, these responses are cell-type and tumor-type-specific. The analysis of mutant p53 alleles has established a gain-of-function role for p53 mutants in metastasis. The development of additional models that can precisely time the oncogenic events in single cells will provide further insight into the evolution of tumors, the importance of the stroma, and the cooperating events that lead to disruption of the p53 pathway. Ultimately, these models should serve to study the effects of novel drugs on tumor response as well as normal homeostasis.
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页数:12
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