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Thioredoxin and protein kinases in redox signaling.

机译:氧化还原信号中的硫氧还蛋白和蛋白激酶。

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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 focuson the ASK1-Trx system. Understanding of such mechanisms may provide the basis for therapeutic interventions in redox-related diseases including various types of cancer.
机译:活性氧(ROS)通过引发多种细胞反应(例如增殖,分化和凋亡),在确定细胞命运中起着至关重要的作用。参与此类ROS诱导的细胞应答的许多细胞内信号转导通路都受到细胞内氧化还原状态的调节,这取决于氧化和还原当量水平之间的平衡。近来,人们已经越来越多地关注硫氧还蛋白(Trx)作为其内在的抗氧化剂活性之外的信号传导中间体的作用。尤其是,Trx通过依赖于氧化还原状态的关联和与凋亡信号调节激酶1(ASK1)(级联的上游调节剂)的解离,参与有丝分裂原活化蛋白激酶(MAPK)级联的控制。这篇综述着重介绍了当前对原型分子机制的理解,通过该机制,氧化还原信号通过ROS响应蛋白激酶转化为信号传导,并特别关注ASK1-Trx系统。对此类机制的理解可以为包括各种类型癌症在内的氧化还原相关疾病的治疗干预提供基础。

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