Selecting protein tyrosine phosphatases as drug targets

被引：165

作者：

van Huijsduijnen, RH ^{[1
]}

Bombrun, A ^{[1
]}

Swinnen, D ^{[1
]}

机构：

[1] Serono Pharmaceut Res Inst, CH-1228 Geneva, Switzerland

来源：

DRUG DISCOVERY TODAY | 2002年 / 7卷 / 19期

关键词：

D O I：

10.1016/S1359-6446(02)02438-8

中图分类号：

R9 [药学];

学科分类号：

1007 ;

摘要：

Protein tyrosine phosphatases (PTPs) have emerged as a new and promising class of signaling targets, since the discovery of PTP1B as a major drug target for diabetes and obesity. Blocking individual PTPs results in the activation of specific tyrosine phosphorylation events, but matching PTPs with such pathways and therapeutic indications is a complex undertaking. The history of PTP1B shows that its unusual knockout phenotype and observations with generic and antisense inhibitors in vivo, but not its classical molecular biology, triggered the rapid development of inhibitors that are today being developed for the clinic.

引用

页码：1013 / 1019

页数：7

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