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TM4SF1的过表达通过激活人前列腺癌中的ERK1/2信号通路来促进细胞转移和生长。

Over-expression of TM4SF1 improves cell metastasis and growth by activating ERK1/2 signaling pathway in human prostate cancer.

作者信息

Chen Junyi, Wang Fubo, Xu Huan, Chen Dong, Liu Weihui, Wang Jialiang

机构信息

Department of Urology, the Second Affiliated Hospital of Fujian Medical University, Quanzhou, China.

出版信息

J BUON. 2019 Nov-Dec;24(6):2531-2538.

PMID:31983129
Abstract

PURPOSE

To explore the effects of Transmembrane-4-L-six-family-1 (TM4SF1) in prostate cancer (PCa), and the related underlying mechanisms.

METHODS

PCa tissues were obtained from 78 patients. PCa cell lines DU145 and RWPE-2 were purchased from American Type Culture Collection (ATCC). Quantitative real-time polymerase chain reaction (qRT-PCR) and Western blot were conducted to analyze the expression of TM4SF1 in PCa tissues and DU145 cells. Plasmid containing over-expressed TM4SF1 was achieved by plasmid transfection. Transwell assay and wound-healing assay were designed to examine the invasion and migration of DU145 cells, whereas colony formation assay and 5-Ethynyl-2'- deoxyuridine (EdU) staining assay were performed to study the proliferation ability of DU145 cells.

RESULTS

TM4SF1 was found over-expressed in PCa tissues and DU145 cells. Over-expression of TM4SF1 significantly activated the extracellular regulated protein kinases (ERK)1/2 signaling pathway, increased the epithelial-mesenchymal transition (EMT) expression, and enhanced the invasion, migration and proliferation of DU145 cells. Further studies revealed that suppression of ERK1/2 signaling pathway nearly resisted the positive effects on DU145 cells induced by TM4SF1 over-expression.

CONCLUSIONS

The present study demonstrated that TM4SF1 enhanced the invasion, migration and proliferation of DU145 cells by activating ERK1/2 signaling pathway.

摘要

目的

探讨跨膜4-L六家族成员1(TM4SF1)在前列腺癌(PCa)中的作用及其相关潜在机制。

方法

从78例患者中获取PCa组织。PCa细胞系DU145和RWPE-2购自美国典型培养物保藏中心(ATCC)。采用定量实时聚合酶链反应(qRT-PCR)和蛋白质免疫印迹法分析PCa组织和DU145细胞中TM4SF1的表达。通过质粒转染构建含过表达TM4SF1的质粒。设计Transwell实验和伤口愈合实验检测DU145细胞的侵袭和迁移能力,同时进行集落形成实验和5-乙炔基-2'-脱氧尿苷(EdU)染色实验研究DU145细胞的增殖能力。

结果

发现TM4SF1在PCa组织和DU145细胞中过表达。TM4SF1的过表达显著激活细胞外调节蛋白激酶(ERK)1/2信号通路,增加上皮-间质转化(EMT)表达,并增强DU145细胞的侵袭、迁移和增殖能力。进一步研究表明,抑制ERK1/2信号通路几乎可抵抗TM4SF1过表达对DU145细胞的积极作用。

结论

本研究表明,TM4SF1通过激活ERK1/2信号通路增强DU145细胞的侵袭、迁移和增殖能力。

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