Mdm2 Affects Genome Stability Independent of p53

被引:51
作者
Bouska, Alyssa [2 ]
Eischen, Christine M. [1 ]
机构
[1] Vanderbilt Univ, Med Ctr, Dept Pathol, Nashville, TN 37232 USA
[2] Univ Nebraska Med Ctr, Dept Pathol & Microbiol, Omaha, NE USA
关键词
STRAND BREAK REPAIR; DNA-DAMAGE; CANCER; OVEREXPRESSION; PATHWAY; MICE; INSTABILITY; EXPRESSION; PROMOTES; DATABASE;
D O I
10.1158/0008-5472.CAN-08-3732
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Mdm2 is a critical negative regulator of the p53 tumor suppressor and is frequently overexpressed in human cancers. However, reports, including our own studies, suggest that Mdm2 has both p53-dependent and p53-independent functions that contribute to genomic instability and transformation when deregulated. We recently elucidated a p53-independent role for Mdm2 in the regulation of the DNA double-strand break repair response, genomic stability, and transformation through interaction with Nbs1, a member of the Mre11/Rad50/Nbs1 DNA double-strand break repair complex. In light of these findings, targeting Mdm2 in human malignancies may have effects other than activating p53. [Cancer Res 2009;69(5):1697-701]
引用
收藏
页码:1697 / 1701
页数:5
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