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RIN1通过Rab25激活表皮生长因子受体(EGFR)信号通路,从而促进肾细胞癌的恶性发展。

RIN1 promotes renal cell carcinoma malignancy by activating EGFR signaling through Rab25.

作者信息

Feng Zi-Hao, Fang Yong, Zhao Liang-Yun, Lu Jun, Wang Yong-Qian, Chen Zhen-Hua, Huang Yong, Wei Jin-Huan, Liang Yan-Ping, Cen Jun-Jie, Pan Yi-Hui, Liao Bing, Chen Wei, Luo Jun-Hang

机构信息

Department of Urology, Sun Yat-sen University, Guangzhou, Guangdong, China.

Department of Urology, The Affiliated Hospital of Kunming University of Science and Technology, Kunming, Yunnan, China.

出版信息

Cancer Sci. 2017 Aug;108(8):1620-1627. doi: 10.1111/cas.13297. Epub 2017 Jul 3.

DOI:10.1111/cas.13297
PMID:28612496
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5543468/
Abstract

We previously identified the important role of RIN1 expression in the prognosis of clear cell renal cell carcinoma (ccRCC). The role of RIN1 in ccRCC malignancy and underlying molecular mechanisms remain unclear. Here we report that ccRCC cells and tissues expressed more RIN1 than normal controls. Gain-of-function and loss-of-function studies demonstrated that RIN1 enhanced ccRCC cell growth, migration and invasion abilities in vitro and promoted tumor growth and metastasis in vivo. Mechanistic studies revealed that RIN1 has an activating effect on EGFR signaling in ccRCC. In addition, we unveil Rab25, a critical GTPase in ccRCC malignancy, as a functional RIN1 interacting partner. Knockdown of Rab25 eliminated the augmentation of carcinoma cell proliferation, migration and invasion by ectopic RIN1. We also confirmed that RIN1 and Rab25 expression correlates with the overall-survival of ccRCC patients from TCGA. These findings suggest that RIN1 plays an important oncogenic role in ccRCC malignancy by activation of EGFR signaling through interacting with Rab25, and RIN1 could be employed as an effective therapeutic target for ccRCC.

摘要

我们之前已经确定了RIN1表达在透明细胞肾细胞癌(ccRCC)预后中的重要作用。RIN1在ccRCC恶性肿瘤中的作用及其潜在分子机制仍不清楚。在此我们报告,ccRCC细胞和组织中RIN1的表达高于正常对照。功能获得和功能丧失研究表明,RIN1在体外增强了ccRCC细胞的生长、迁移和侵袭能力,并在体内促进了肿瘤生长和转移。机制研究显示,RIN1对ccRCC中的EGFR信号具有激活作用。此外,我们发现Rab25是ccRCC恶性肿瘤中的一种关键GTP酶,是RIN1的功能性相互作用伙伴。敲低Rab25可消除异位RIN1对癌细胞增殖、迁移和侵袭的增强作用。我们还证实,RIN1和Rab25的表达与来自TCGA的ccRCC患者的总生存期相关。这些发现表明,RIN1通过与Rab25相互作用激活EGFR信号,在ccRCC恶性肿瘤中发挥重要的致癌作用,并且RIN1可作为ccRCC的有效治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b206/5543468/bc592b389856/CAS-108-1620-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b206/5543468/b92ad79390d3/CAS-108-1620-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b206/5543468/569ac0b70f69/CAS-108-1620-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b206/5543468/0c3ec386cb95/CAS-108-1620-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b206/5543468/68b750ac6a9c/CAS-108-1620-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b206/5543468/0c99f861af03/CAS-108-1620-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b206/5543468/bc592b389856/CAS-108-1620-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b206/5543468/b92ad79390d3/CAS-108-1620-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b206/5543468/569ac0b70f69/CAS-108-1620-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b206/5543468/0c3ec386cb95/CAS-108-1620-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b206/5543468/68b750ac6a9c/CAS-108-1620-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b206/5543468/0c99f861af03/CAS-108-1620-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b206/5543468/bc592b389856/CAS-108-1620-g006.jpg

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