Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas 77030, USA.
Cold Spring Harb Perspect Biol. 2009 Dec;1(6):a001081. doi: 10.1101/cshperspect.a001081. Epub 2009 Nov 4.
The p53 tumor suppressor is a multifaceted transcription factor that responds to a diverse array of stresses that include DNA damage and aberrant oncogene signaling. On activation, p53 prevents the emergence of cancer cells by initiating cell cycle arrest, senescence (terminal cell cycle arrest), or apoptosis. Although its role in assuring longevity by suppressing cancer is well established, recent studies obtained largely from genetically engineered mouse models suggest that p53 may regulate longevity and aging. In some contexts, it appears that altered p53 activity may enhance longevity, and in others, it appears to suppress longevity and accelerate aging phenotypes. Here, we discuss how genetically engineered mouse models have been used to explore antiproliferative functions of p53 in cancer suppression and how mouse models with altered aging phenotypes have shed light on how p53 might influence the aging process.
p53 肿瘤抑制因子是一种多效转录因子,可响应多种应激,包括 DNA 损伤和异常癌基因信号。激活后,p53 通过启动细胞周期停滞、衰老(细胞周期停滞的终末阶段)或细胞凋亡来防止癌细胞的出现。尽管其通过抑制癌症来确保长寿的作用已得到充分证实,但最近的研究主要来自基因工程小鼠模型表明,p53 可能调节寿命和衰老。在某些情况下,改变 p53 的活性似乎可以延长寿命,而在其他情况下,它似乎会抑制寿命并加速衰老表型。在这里,我们讨论了基因工程小鼠模型如何用于探索 p53 在癌症抑制中的抗增殖功能,以及改变衰老表型的小鼠模型如何阐明 p53 如何影响衰老过程。