结节性硬化症复合体病理生理学的新见解:细胞生长中mTOR-和hippo-YAP通路的串扰。

Rare diseases (Austin, Tex.) Pub Date : 2015-02-23 eCollection Date: 2015-01-01 DOI:10.1080/21675511.2015.1016701
Patricia E Dill, Ning Liang, Mario Pende
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引用次数: 5

摘要

结节性硬化症(TSC)是一种导致错构瘤不受控制生长的遗传性疾病,累及不同的器官系统。在过去的十年中,mTORC1通路的失调被证明是TSC中肿瘤生长的主要驱动因素。最近,在mTORC1和Hippo-YAP通路之间发现了一个新的串扰,Hippo-YAP通路是另一个主要的细胞信号级联,控制细胞生长和器官大小。阐明这种联系是理解TSC复杂性的重要一步,从而实现新的药理靶点和治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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New insights into the pathophysiology of the tuberous sclerosis complex: Crosstalk of mTOR- and hippo-YAP pathways in cell growth.

Tuberous Sclerosis Complex (TSC) is a genetic disease causing uncontrolled growth of hamartomas involving different organ systems. In the last decade, dysregulation of the mTORC1 pathway was shown to be a main driver of tumor growth in TSC. Recently, a new crosstalk was detected between the mTORC1 and the Hippo-YAP pathway, another major cell signaling cascade controlling cell growth and organ size. Elucidating this connection is an important step in understanding the complexity of TSC, enabling new pharmacological targets and therapeutical options.

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