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转化生长因子-β1介导长链非编码RNA GAPLINC的表达以促进非小细胞肺癌的迁移和侵袭。

TGF-β1 mediates lncRNA GAPLINC expression to promote the migration and invasion of non-small cell lung cancer.

作者信息

Zhao Jianqiang, Wang Changmei, Liu Shuai, Su Xinyou, Ouyang Aimei

机构信息

Department of Oncology, Jinan Central Hospital, Jinan City, Shandong Province 250012, People's Republic of China.

出版信息

Onco Targets Ther. 2019 Aug 2;12:6175-6180. doi: 10.2147/OTT.S207079. eCollection 2019.

DOI:10.2147/OTT.S207079
PMID:31447565
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6683965/
Abstract

The present study aims to investigate the involvement of lncRNA GAPLINC in non-small lung cancer (NSCLC). The study included 70 patients with NSCLC (39 males and 31 females, 33 to 68 years, 49.3 ± 6.4 years). RT-qPCR, transient cell transfections, measurement of in vitro cell migration and invasion abilities and western blot were carrying out during the research. We showed that GAPLINC was up-regulated in NSCLC tissues and positively correlated with TGF-β1. In vitro cell experiment showed that over-expression of TGF-β1 significantly up-regulated the expression of GAPLINC, while over-expression of GAPLINC failed to affect TGF-β1. Follow-up study showed that high GAPLINC level in NSCLC tissue was closely correlated with poor survival rate of NSCLC patients. Over-expressions of TGF-β1 and GAPLINC resulted to accelerated migration and invasion of NSCLC cells. In addition, the silencing of GAPLINC siRNA attenuated the effect of TGF-β1 treatment. TGF-β1 may mediate lncRNA GAPLINC expression to promote NSCLC cell invasion and migration.

摘要

本研究旨在探究长链非编码RNA GAPLINC在非小细胞肺癌(NSCLC)中的作用。该研究纳入了70例NSCLC患者(39例男性和31例女性,年龄33至68岁,平均49.3±6.4岁)。研究过程中进行了逆转录定量聚合酶链反应(RT-qPCR)、瞬时细胞转染、体外细胞迁移和侵袭能力检测以及蛋白质免疫印迹法。我们发现,GAPLINC在NSCLC组织中表达上调,且与转化生长因子-β1(TGF-β1)呈正相关。体外细胞实验表明,TGF-β1过表达显著上调GAPLINC的表达,而GAPLINC过表达则未影响TGF-β1。随访研究显示,NSCLC组织中GAPLINC水平高与NSCLC患者生存率低密切相关。TGF-β1和GAPLINC过表达导致NSCLC细胞迁移和侵袭加速。此外,GAPLINC小干扰RNA(siRNA)沉默减弱了TGF-β1处理的效果。TGF-β1可能通过介导长链非编码RNA GAPLINC的表达来促进NSCLC细胞的侵袭和迁移。

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