Thioredoxin and protein kinases in redox signaling

被引:132
作者
Fujino, Go
Noguchi, Takuya
Takeda, Kohsuke
Ichijo, Hidenori
机构
[1] Univ Tokyo, Grad Sch Pharmaceut Sci, Lab Cell Signalling, Japan Sci & Technol Corp,Bunkyo Ku, Tokyo 1130033, Japan
[2] Ctr Excellence COE Program, Strateg Approach Drug Discovery & Dev Pharmaceut, Tokyo 1130033, Japan
关键词
reactive oxygen species; thioredoxin; ASK1; MAPK; nucleoredoxin;
D O I
10.1016/j.semcancer.2006.09.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Reactive oxygen species (ROS) play critical roles for the determination of cell fate by eliciting a wide variety of cellular responses, such as proliferation, differentiation and apoptosis. Many intracellular signaling pathways involved in such ROS-induced cellular responses are regulated by the intracellular redox state, which depends on the balance between the levels of oxidizing and reducing equivalents. Recently, increasing attention has been paid to the roles of thioredoxin (Trx) as a signaling intermediate beyond its intrinsic antioxidant activity. Especially, Trx participates in the control of the mitogen-activated protein kinase (MAPK) cascades through the redox state-dependent association and dissociation with apoptosis signal-regulating kinase 1 (ASK1), an upstream regulator of the cascades. This review highlights the current understanding of prototypical molecular mechanisms by which the redox signal is converted into the signaling through ROS-responsive protein kinases, with a special focus on the ASK1-Trx system. Understanding of such mechanisms may provide the basis for therapeutic interventions in redox-related diseases including various types of cancer. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:427 / 435
页数:9
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