Mdm2-mediated ubiquitylation: p53 and beyond

被引:257
|
作者
Marine, J-C [1 ]
Lozano, G. [2 ]
机构
[1] Univ Ghent VIB, Lab Mol Canc Biol, B-9052 Ghent, Belgium
[2] Univ Texas Grad Sch Biomed Sci, Univ Texas MD Anderson Canc Ctr, Dept Genet, Houston, TX 77030 USA
来源
CELL DEATH AND DIFFERENTIATION | 2010年 / 17卷 / 01期
关键词
MDM2; p53; ubiquitylation; cancer therapy; UBIQUITIN LIGASE ACTIVITY; NUCLEAR EXPORT; RING DOMAIN; MDM2-DEFICIENT MICE; EMBRYONIC LETHALITY; TUMOR SUPPRESSION; ONCOPROTEIN MDM2; C-TERMINUS; PROTEIN; DEGRADATION;
D O I
10.1038/cdd.2009.68
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 really interesting genes (RING)-finger-containing oncoprotein, Mdm2, is a promising drug target for cancer therapy. A key Mdm2 function is to promote ubiquitylation and proteasomal-dependent degradation of the tumor suppressor protein p53. Recent reports provide novel important insights into Mdm2-mediated regulation of p53 and how the physical and functional interactions between these two proteins are regulated. Moreover, a p53-independent role of Mdm2 has recently been confirmed by genetic data. These advances and their potential implications for the development of new cancer therapeutic strategies form the focus of this review. Cell Death and Differentiation (2010) 17, 93-102; doi:10.1038/cdd.2009.68; published online 5 June 2009
引用
收藏
页码:93 / 102
页数:10
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