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Akt-mTOR信号通路及其与癌症的相关性。

The Akt-mTOR tango and its relevance to cancer.

作者信息

Hay Nissim

机构信息

Department of Biochemistry and Molecular Genetics, University of Illinois at Chicago College of Medicine, 60607, USA.

出版信息

Cancer Cell. 2005 Sep;8(3):179-83. doi: 10.1016/j.ccr.2005.08.008.

Abstract

The downstream effector of PI3K, Akt, is frequently hyperactivated in human cancers. A critical downstream effector of Akt, which contributes to tumorigenesis, is mTOR. In the PI3K/Akt/mTOR pathway, Akt is flanked by two tumor suppressors: PTEN, acting as a brake upstream of Akt, and TSC1/TSC2 heterodimer, acting as a brake downstream of Akt and upstream of mTOR. In the absence of the TSC1/TSC2 brake, mTOR activity is unleashed to inhibit Akt via an inhibitory feedback mechanism. Two recent studies used mouse genetics to assess the roles of PTEN and TSC2 in cancer, underscoring the importance of Akt-mTOR interplay for cancer progression and therapy.

摘要

PI3K的下游效应器Akt在人类癌症中经常过度激活。Akt的一个关键下游效应器mTOR,对肿瘤发生起作用。在PI3K/Akt/mTOR通路中,Akt两侧有两个肿瘤抑制因子:PTEN,在Akt上游起制动作用;TSC1/TSC2异二聚体,在Akt下游和mTOR上游起制动作用。在没有TSC1/TSC2制动的情况下,mTOR活性被释放,通过抑制性反馈机制抑制Akt。最近的两项研究利用小鼠遗传学评估了PTEN和TSC2在癌症中的作用,强调了Akt-mTOR相互作用对癌症进展和治疗的重要性。

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