Classic and novel roles of p53:: prospects for anticancer therapy

被引:111
作者
Fuster, Jose J.
Sanz-Gonzalez, Silvia M.
Moll, Ute M.
Andres, Vicente [1 ]
机构
[1] CSIC, Vasc Biol Unit, IBV, Spanish Council Sci Res, Valencia 46010, Spain
[2] SUNY Stony Brook, Dept Pathol, Stony Brook, NY 11794 USA
关键词
D O I
10.1016/j.molmed.2007.03.002
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
The tumor suppressor p53 is a transcription factor that is frequently inactivated in human tumors. Therefore, restoring its function has been considered an attractive approach to restrain cancer. Typically, p53-dependent growth arrest, senescence and apoptosis of tumor cells have been attributed to transcriptional activity of nuclear p53. Notably, wild-type p53 gain-of-function enhances cancer resistance in the mouse, but it also accelerates aging in some models, possibly due to altered p53 activity. Therefore, the emerging evidence of mitochondrial transcription-independent activities of p53 has raised high expectations. Here, we review new developments in transcription-dependent and transcription-independent p53 functions, recent advances in targeting p53 for cancer treatment and the pitfalls of moving from the laboratory research to the clinical setting.
引用
收藏
页码:192 / 199
页数:8
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