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Inhibition of the p53-hdm2 interaction with low molecular weight compounds.

作者信息

Chène Patrick

机构信息

Novartis, Oncology, Department, Basel, Switzerland.

出版信息

Cell Cycle. 2004 Apr;3(4):460-1. doi: 10.4161/cc.3.4.791. Epub 2004 Apr 1.

Abstract

The hdm2 protein, upon binding to p53, inhibits its tumor suppressor activity. The inhibition of the p53-hdm2 interaction represents therefore a new therapeutic strategy to activate wild type p53 in tumors. Potent low molecular weight compounds inhibiting this protein-protein interaction, which are active in vivo, have just been identified. This offers new perspectives and hopes in this research area.

摘要

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