Signaling to p53: Ribosomal Proteins Find Their Way

被引:461
|
作者
Zhang, Yanping [1 ,2 ,3 ]
Lu, Hua [4 ,5 ]
机构
[1] Univ N Carolina, Sch Med, Dept Radiat Oncol, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Sch Med, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Sch Med, Dept Pharmacol, Chapel Hill, NC 27599 USA
[4] Indiana Univ Sch Med, Dept Biochem & Mol Biol, Indianapolis, IN 46202 USA
[5] Indiana Univ Sch Med, Simon Canc Ctr, Indianapolis, IN 46202 USA
基金
美国国家卫生研究院;
关键词
UBIQUITIN LIGASE ACTIVITY; DIAMOND-BLACKFAN ANEMIA; NON-ONCOGENE ADDICTION; ZINC-FINGER DOMAIN; C-MYC; ACTIVATES P53; CELL-CYCLE; EMBRYONIC LETHALITY; ONCOPROTEIN MDM2; IN-VIVO;
D O I
10.1016/j.ccr.2009.09.024
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Inherently disparate cell growth and division, which are intimately coupled through a delicate network of intracellular and extracellular signaling, require ribosomal biogenesis. A number of events imparting instability to ribosomal biogenesis can cause nucleolar stress. In response to this stress, several ribosomal proteins bind to MDM2 and block MDM2-mediated p53 ubiquitination and degradation, resulting in p53-dependent cell cycle arrest. By doing so, the ribosomal proteins play a crucial role in connecting deregulated cell growth with inhibition of cell division. The ribosomal protein-MDM2-p53 signaling pathway provides a molecular switch that may constitute a surveillance network monitoring the integrity of ribosomal biogenesis.
引用
收藏
页码:369 / 377
页数:9
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