Inhibitors of the p53/hdm2 protein-protein interaction-path to the clinic

被引:57
作者
Carry, Jean-Christophe [1 ]
Garcia-Echeverria, Carlos [1 ]
机构
[1] Sanofi, Oncol Drug Discovery & Preclin Dev, F-94400 Vitry Sur Seine, France
关键词
p53; hdm2; hdmx; Protein-protein interaction; Anticancer agent; STRUCTURE-BASED DESIGN; STAPLED P53; IN-VIVO; MDM2; ANTAGONISTS; ACTIVATION; DISCOVERY; POTENT; DERIVATIVES;
D O I
10.1016/j.bmcl.2013.03.034
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A growing number of the elements identified in intracellular signaling events that affect cell growth and transformation are proteins that physically interact with each other via domains or specifically recognized amino acid sequences. Some of these intracellular protein-protein interactions are attractive targets for anticancer targeted therapy, but progress in this field has been compromised by the paucity of compounds with suitable biological profiles and pharmacological properties. This Letter covers salient achievements in the identification and development of inhibitors of the p53-hdm2 protein-protein interaction, and highlights different screening techniques and structure-based design approaches that may be brought to bear on the discovery and development of inhibitors of other therapeutically relevant intracellular protein-protein interactions. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2480 / 2485
页数:6
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