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类formin2通过调节Rho/ROCK信号通路促进结直肠癌的肌动蛋白组装和细胞侵袭。

Formin-like2 regulates Rho/ROCK pathway to promote actin assembly and cell invasion of colorectal cancer.

作者信息

Zeng Yuanfeng, Xie Huijun, Qiao Yudan, Wang Jianmei, Zhu Xiling, He Guoyang, Li Yuling, Ren Xiaoli, Wang Feifei, Liang Li, Ding Yanqing

机构信息

Department of Pathology, Southern Medical University, Guangzhou, China.

Department of Pathology, the People's Hospital, Nanchang, China.

出版信息

Cancer Sci. 2015 Oct;106(10):1385-93. doi: 10.1111/cas.12768.

Abstract

Formin-like2 (FMNL2) is a member of the diaphanous-related formins family, which act as effectors and upstream modulators of Rho GTPases signaling and control the actin-dependent processes, such as cell motility or invasion. FMNL2 has been identified as promoting the motility and metastasis in colorectal carcinoma (CRC). However, whether FMNL2 regulates Rho signaling to promote cancer cell invasion remains unclear. In this study, we demonstrated an essential role for FMNL2 in the activations of Rho/ROCK pathway, SRF transcription or actin assembly, and subsequent CRC cell invasion. FMNL2 could activate Rho/ROCK pathway, and required ROCK to promote CRC cell invasion. Moreover, FMNL2 promoted the formation of filopodia and stress fiber, and activated the SRF transcription in a Rho-dependent manner. We also demonstrated that FMNL2 was necessary for LPA-induced invasion, RhoA/ROCK activation, actin assembly and SRF activation. FMNL2 was an essential component of LPA signal transduction toward RhoA by directly interacting with LARG. LARG silence inhibited RhoA/ROCK pathway and CRC cell invasion. Collectively, these data indicate that FMNL2, acting as upstream of RhoA by interacting with LARG, can promote actin assembly and CRC cell invasion through a Rho/ROCK-dependent mechanism.

摘要

formin样蛋白2(FMNL2)是与透明质酸相关的formin家族成员,作为Rho GTP酶信号传导的效应器和上游调节剂,控制肌动蛋白依赖性过程,如细胞运动或侵袭。FMNL2已被确定为促进结直肠癌(CRC)的运动和转移。然而,FMNL2是否通过调节Rho信号来促进癌细胞侵袭仍不清楚。在本研究中,我们证明了FMNL2在Rho/ROCK途径激活、血清反应因子(SRF)转录或肌动蛋白组装以及随后的CRC细胞侵袭中起关键作用。FMNL2可激活Rho/ROCK途径,且需要ROCK来促进CRC细胞侵袭。此外,FMNL2促进丝状伪足和应力纤维的形成,并以Rho依赖性方式激活SRF转录。我们还证明,FMNL2是溶血磷脂酸(LPA)诱导的侵袭、RhoA/ROCK激活、肌动蛋白组装和SRF激活所必需的。FMNL2通过直接与LARG相互作用,是LPA向RhoA信号转导的重要组成部分。LARG沉默抑制RhoA/ROCK途径和CRC细胞侵袭。总体而言,这些数据表明,FMNL2通过与LARG相互作用作为RhoA的上游,可以通过Rho/ROCK依赖性机制促进肌动蛋白组装和CRC细胞侵袭。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e19/4638017/7f7191f07fc4/cas0106-1385-f1.jpg

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