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YAP通过ARHGAP29调节肌动蛋白动力学并促进转移。

YAP Regulates Actin Dynamics through ARHGAP29 and Promotes Metastasis.

作者信息

Qiao Yiting, Chen Jianxiang, Lim Ying Bena, Finch-Edmondson Megan Louise, Seshachalam Veerabrahma Pratap, Qin Lei, Jiang Tingting, Low Boon Chuan, Singh Himanshu, Lim Chwee Teck, Sudol Marius

机构信息

Department of Physiology, Yong Loo Lin School of Medicine, National University of Singapore, MD9, 2 Medical Drive, Singapore 117593, Singapore.

National Cancer Centre of Singapore, 11 Hospital Drive, Singapore 169610, Singapore; Institute of Molecular and Cell Biology (IMCB), Agency for Science, Technology and Research, Singapore, 61 Biopolis Drive, Singapore 138673, Singapore.

出版信息

Cell Rep. 2017 May 23;19(8):1495-1502. doi: 10.1016/j.celrep.2017.04.075.

Abstract

Yes-associated protein (YAP) is regulated by mechanical cues via the interaction of the Hippo pathway with cytoskeleton. Previous studies showed that YAP plays a role in regulating the actomyosin network by suppressing Rho GTPase in medaka fish. Here, we identify Rho GTPase activating protein 29 (ARHGAP29) as a transcriptional target of YAP in a human gastric cancer cell line. YAP promotes the expression of ARHGAP29 to suppress the RhoA-LIMK-cofilin pathway, destabilizing F-actin. The overexpression of YAP causes cytoskeletal rearrangement by altering the dynamics of F-actin/G-actin turnover, thus promoting migration. In a mouse model, circulating tumor cells (CTCs) exhibit an increased ARHGAP29 RNA level compared with cells at primary tumor sites, and the metastatic potential of CTCs is positively correlated with ARHGAP29 expression. Moreover, increased ARHGAP29 expression is correlated with shortened survival of human gastric cancer patients. Our study provides a model to understand YAP's contribution to cancer metastasis via regulation of actin dynamics.

摘要

Yes相关蛋白(YAP)通过Hippo信号通路与细胞骨架的相互作用受到机械信号的调控。先前的研究表明,YAP在青鳉鱼中通过抑制Rho GTP酶在调节肌动球蛋白网络中发挥作用。在此,我们在人胃癌细胞系中鉴定出Rho GTP酶激活蛋白29(ARHGAP29)是YAP的转录靶点。YAP促进ARHGAP29的表达以抑制RhoA-LIMK-丝切蛋白通路,使F-肌动蛋白不稳定。YAP的过表达通过改变F-肌动蛋白/G-肌动蛋白周转的动力学导致细胞骨架重排,从而促进迁移。在小鼠模型中,循环肿瘤细胞(CTC)与原发性肿瘤部位的细胞相比,ARHGAP29 RNA水平升高,且CTC的转移潜能与ARHGAP29表达呈正相关。此外,ARHGAP29表达增加与人类胃癌患者生存期缩短相关。我们的研究提供了一个模型,以了解YAP通过调节肌动蛋白动力学对癌症转移的作用。

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