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微小RNA-361靶向肾母细胞瘤1以抑制非小细胞肺癌细胞的生长、迁移和侵袭。

microRNA-361 targets Wilms' tumor 1 to inhibit the growth, migration and invasion of non-small-cell lung cancer cells.

作者信息

Yang Shuxiang, Zhang Yingchao, Zhao Xin, Wang Jingzheng, Shang Jianjing

机构信息

Department of General Internal Medicine, Tianjin Hospital, Tianjin 300211, P.R. China.

Department of Respiration, Tianjin Baodi Hospital, Tianjin 301800, P.R. China.

出版信息

Mol Med Rep. 2016 Dec;14(6):5415-5421. doi: 10.3892/mmr.2016.5858. Epub 2016 Oct 19.

Abstract

The expression and functions of microRNA-361 (miR-361) have been studied in various human cancers. However, its expression and role in non‑small‑cell lung cancer (NSCLC) remains unclear. In the present study, the expression levels of miR‑361 in NSCLC tissues and cell lines were determined using reverse transcription‑quantitative polymerase chain reaction (RT‑qPCR). In addition, the effect of miR‑361 on the proliferation, migration and invasion of NSCLC cells was assessed. Furthermore, a dual‑Luciferase reporter assay, RT‑qPCR and western blotting were performed to investigate whether miR‑361 directly targeted the 3' untranslated region of Wilms' tumor 1 (WT1). The results of the present study revealed that miR‑361 was downregulated in NSCLC tissues and cell lines. Enforced expression of miR‑361 suppressed the proliferation, migration and invasion of NSCLC cells. WT1 was identified as a direct target gene of miR‑361 in NSCLC. Furthermore, knockdown of WT1 had similar effects to miR‑361 overexpression in NSCLC cells. The present study provided novel insights into the molecular mechanism underlying the rapid growth and metastasis of NSCLC, and identified the association between miR‑361 and WT1 as a potential therapeutic target for the treatment of NSCLC.

摘要

微小RNA-361(miR-361)的表达及功能已在多种人类癌症中得到研究。然而,其在非小细胞肺癌(NSCLC)中的表达及作用仍不清楚。在本研究中,采用逆转录定量聚合酶链反应(RT-qPCR)测定miR-361在NSCLC组织和细胞系中的表达水平。此外,评估了miR-361对NSCLC细胞增殖、迁移和侵袭的影响。进一步进行双荧光素酶报告基因检测、RT-qPCR和蛋白质印迹法,以研究miR-361是否直接靶向肾母细胞瘤1(WT1)的3'非翻译区。本研究结果显示,miR-361在NSCLC组织和细胞系中表达下调。miR-361的过表达抑制了NSCLC细胞的增殖、迁移和侵袭。WT1被确定为NSCLC中miR-361的直接靶基因。此外,敲低WT1在NSCLC细胞中具有与miR-361过表达类似的作用。本研究为NSCLC快速生长和转移的分子机制提供了新见解,并确定了miR-361与WT1之间的关联作为NSCLC治疗的潜在靶点。

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