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自噬途径作为癌症药物开发的新靶点。

Autophagic pathways as new targets for cancer drug development.

机构信息

West China Hospital, Sichuan University, Chengdu, China.

出版信息

Acta Pharmacol Sin. 2010 Sep;31(9):1154-64. doi: 10.1038/aps.2010.118. Epub 2010 Aug 9.

Abstract

Autophagy is an evolutionarily conserved lysosomal self-digestion process involved in degradation of long-lived proteins and damaged organelles. In recent years, increasing evidence indicates that autophagy is associated with a number of pathological processes, including cancer. In this review, we focus on the recent studies of the evolutionarily conserved autophagy-related genes (ATGs) that are implicated in autophagosome formation and the pathways involved. We discuss several key autophagic mediators (eg, Beclin-1, UVRAG, Bcl-2, Class III and I PI3K, mTOR, and p53) that play pivotal roles in autophagic signaling networks in cancer. We discuss the Janus roles of autophagy in cancer and highlighted their relationship to tumor suppression and tumor progression. We also present some examples of targeting ATGs and several protein kinases as anticancer strategy, and discuss some autophagy-modulating agents as antitumor agents. A better understanding of the relationship between autophagy and cancer would ultimately allow us to harness autophagic pathways as new targets for drug discovery in cancer therapeutics.

摘要

自噬是一种进化上保守的溶酶体自我消化过程,参与长寿命蛋白质和受损细胞器的降解。近年来,越来越多的证据表明自噬与许多病理过程有关,包括癌症。在这篇综述中,我们重点介绍了最近关于参与自噬体形成和相关途径的进化上保守的自噬相关基因(ATGs)的研究。我们讨论了几个关键的自噬介体(如 Beclin-1、UVRAG、Bcl-2、III 类和 I 型 PI3K、mTOR 和 p53),它们在癌症中的自噬信号网络中发挥关键作用。我们讨论了自噬在癌症中的双刃剑作用,并强调了它们与肿瘤抑制和肿瘤进展的关系。我们还介绍了一些靶向 ATGs 和几种蛋白激酶作为抗癌策略的例子,并讨论了一些作为抗肿瘤剂的自噬调节剂。更好地理解自噬与癌症之间的关系最终将使我们能够利用自噬途径作为癌症治疗药物发现的新靶点。

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Autophagic pathways as new targets for cancer drug development.自噬途径作为癌症药物开发的新靶点。
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