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微小RNA-938通过调控肺腺癌细胞中的RNA结合基序蛋白5促进细胞增殖。

miR-938 promotes cell proliferation by regulating RBM5 in lung adenocarcinoma cells.

作者信息

Qian Taotao, Shi Shunbin, Xie Lincen, Zhu Yong

机构信息

Department of Thoracic Surgery, Suzhou Ninth People's Hospital, 2666 Ludang Road, Taihu New City, Wujiang District, Suzhou, Jiangsu Province, 215000, China.

Department of Thoracic Surgery, Wujiang People's Hospital Affiliated to Nantong University, 2666 Ludang Road, Taihu New City, Wujiang District, Suzhou, Jiangsu Province, 215000, China.

出版信息

Cell Biol Int. 2020 Jan;44(1):295-305. doi: 10.1002/cbin.11233. Epub 2019 Sep 25.

Abstract

A growing body of research suggests that microRNAs (miRNAs) may play a key part in the progression of various cancers, including lung adenocarcinoma (LUAD). However, the expression and mechanism of miR-938 (microRNA-938) in LUAD have not been defined. Compared with adjacent tissues, the level of miR-938 was up-regulated in LUAD tissues. miR-938 expression was significantly associated with tumor size. In vitro assays indicated that miR-938 expression was also increased in the LUAD cell lines. Overexpression of miR-938 promoted LUAD cell proliferation, whereas down-regulation of miR-938 had the opposite effect. We identified RNA-binding protein 5 (RBM5) as a potential target gene of miR-938 in LUAD. Expression of RBM5 was down-regulated in LUAD tumor tissues and negatively correlated with expression of miR-938. Up-regulation of RBM5 reversed cell proliferation by inhibition of miR-938 expression in LUAD cells. These results showed that miR-938 may act as an oncogenic miRNA by targeting RBM5 in LUAD, indicating that miR-938 could be used as a potential therapeutic target for LUAD patients.

摘要

越来越多的研究表明,微小RNA(miRNA)可能在包括肺腺癌(LUAD)在内的各种癌症进展中起关键作用。然而,miR-938(微小RNA-938)在LUAD中的表达及机制尚未明确。与邻近组织相比,LUAD组织中miR-938水平上调。miR-938表达与肿瘤大小显著相关。体外实验表明,LUAD细胞系中miR-938表达也增加。miR-938过表达促进LUAD细胞增殖,而miR-938下调则产生相反作用。我们确定RNA结合蛋白5(RBM5)是LUAD中miR-938的潜在靶基因。LUAD肿瘤组织中RBM5表达下调,且与miR-938表达呈负相关。RBM5上调通过抑制LUAD细胞中miR-938表达逆转细胞增殖。这些结果表明,miR-938可能通过靶向LUAD中的RBM5发挥致癌性miRNA的作用,这表明miR-938可作为LUAD患者的潜在治疗靶点。

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