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MTA1促进人胃癌细胞的增殖和侵袭。

MTA1 promotes proliferation and invasion in human gastric cancer cells.

作者信息

Yao Yuan, Feng Shuting, Xiao Mingming, Li Yan, Yang Li, Gong Jiao

机构信息

Digestive System Department, The People's Hospital of Liaoning Province, Shenyang, Liaoning, People's Republic of China.

Department of Pathology, The People's Hospital of Liaoning Province, Shenyang, Liaoning, People's Republic of China.

出版信息

Onco Targets Ther. 2015 Jul 20;8:1785-94. doi: 10.2147/OTT.S85383. eCollection 2015.

Abstract

Although metastasis-associated protein 1 (MTA1) has been widely linked to tumor metastasis, the relevant mechanisms remain to be elucidated, especially in gastric cancer. The aim of this study was to examine whether the MTA1 gene is associated with the process of proliferation and invasion by regulating several molecular targets in gastric cancer. MTA1 expression in 61 gastric cancer tissue and adjacent noncancerous tissues was analyzed by immunohistochemistry. The prognostic value of MTA1 for overall survival and disease-free survival was determined by Kaplan-Meier estimates, and the significance of differences between curves was evaluated by the log-rank test. Furthermore, overexpression of MTA1 in SGC7901 and BGC823 cells promoted cell cycle progression, cell adhesion, and cell invasion. Our study found that MTA1 is overexpressed in gastric cancers, which contributes to malignant cell growth by facilitating cell cycle progression through upregulation of cyclin D1 and accelerates the migration and invasion of human gastric cancer cells by regulating expression of fibronectin and MMP2/MMP9. Taken together, MTA1 was involved in the pathogenesis of gastric cancer and might be a candidate therapeutic target in gastric cancer.

摘要

尽管转移相关蛋白1(MTA1)已被广泛认为与肿瘤转移有关,但其相关机制仍有待阐明,尤其是在胃癌中。本研究的目的是通过调节胃癌中的几个分子靶点,研究MTA1基因是否与增殖和侵袭过程相关。采用免疫组织化学方法分析61例胃癌组织及癌旁非癌组织中MTA1的表达。通过Kaplan-Meier估计确定MTA1对总生存期和无病生存期的预后价值,并通过对数秩检验评估曲线间差异的显著性。此外,MTA1在SGC7901和BGC823细胞中的过表达促进了细胞周期进程、细胞黏附和细胞侵袭。我们的研究发现,MTA在胃癌中过表达,通过上调细胞周期蛋白D1促进细胞周期进程,从而促进恶性细胞生长,并通过调节纤连蛋白和MMP2/MMP9的表达加速人胃癌细胞的迁移和侵袭。综上所述,MTA1参与了胃癌的发病机制,可能是胃癌的一个候选治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0e4/4516181/ca6027c866ed/ott-8-1785Fig1.jpg

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