Disrupting the p53-mdm2 interaction as a potential therapeutic modality

被引:8
作者
Moll, UM [1 ]
Zaika, A [1 ]
机构
[1] SUNY Stony Brook, Dept Pathol, Stony Brook, NY 11794 USA
关键词
D O I
10.1054/drup.2000.0160
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
P53 and mdm2 are linked to each other through a negative feedback loop. P53 transactivates mdm2, but mdm2, in turn, is a major opponent of p53. Mdm2 promotes p53 degradation through a ubiquitin-dependent pathway on 26S proteasomes and is thought to be largely responsible for the very low levels of p53 protein in unstressed cells. The rationale for targeting the p53-mdm2 interaction therapeutically lies in the ability to activate p53 in all those tumors that retain wild type p53. (C) 2900 Harcourt Publishers Ltd.
引用
收藏
页码:217 / 221
页数:5
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