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miR-196a对lncRNA GAS5的负调控抑制食管鳞状细胞癌的生长。

Negative regulation of lncRNA GAS5 by miR-196a inhibits esophageal squamous cell carcinoma growth.

作者信息

Wang Kai, Li Juan, Xiong Gang, He Gang, Guan Xingying, Yang Kang, Bai Yun

机构信息

Department of Medical Genetics, Department of Basic Medicine, Third Military Medical University, Chongqing 400038, PR China.

Department of Thoracic and Cardiac Surgery, Southwest Hospital, Third Military Medical University, Chongqing 400038, PR China.

出版信息

Biochem Biophys Res Commun. 2018 Jan 1;495(1):1151-1157. doi: 10.1016/j.bbrc.2017.11.119. Epub 2017 Nov 21.

Abstract

MiR-196a could play important roles in carcinogenesis by targeting many protein coding genes. However, little is known about whether miR-196a can target any long non-coding RNAs (lncRNAs). In the present study, we screen lncRNAs which are regulated by miRNA-196a in human esophageal squamous cell carcinoma (ESCC). We found that miR-196a could suppress the expression of lncRNA growth arrest-specific 5(GAS5). GAS5 is frequently down-regulated in 86 paired human ESCC tissues. Importantly, there was lower GAS5 expression in the late stage of ESCC patients. The reduced expression of GAS5 in ESCC may not be related to DNA methylation but related to the high expression of miR-196a. In vitro and in vivo studies indicated that GAS5 could inhibit the growth of ESCC cells. Using Chromatin Isolation by RNA Purification-qPCR, we found that miR-196a could bind to GAS5. The Luciferase Reporter Assay indicated that miR-196a could bind to the seventh exon of GAS5. Additionally, both GAS5 and miR-196a could bind to Ago2 which is a key component of the RNA-induced silencing complex (RISC). Together, these results suggest that GAS5 functions as a tumor suppressor gene in ESCC and is regulated by miR-196a involved in RISC.

摘要

MiR-196a可通过靶向许多蛋白质编码基因在肿瘤发生过程中发挥重要作用。然而,关于miR-196a是否能靶向任何长链非编码RNA(lncRNA)却知之甚少。在本研究中,我们筛选了在人食管鳞状细胞癌(ESCC)中受miRNA-196a调控的lncRNA。我们发现miR-196a可抑制长链非编码RNA生长停滞特异性5(GAS5)的表达。在86对人ESCC组织中,GAS5经常下调。重要的是,ESCC患者晚期的GAS5表达较低。ESCC中GAS5表达降低可能与DNA甲基化无关,而与miR-196a的高表达有关。体外和体内研究表明,GAS5可抑制ESCC细胞的生长。通过RNA纯化-qPCR进行染色质分离,我们发现miR-196a可与GAS5结合。荧光素酶报告基因检测表明,miR-196a可与GAS5的第七外显子结合。此外,GAS5和miR-196a均可与RNA诱导沉默复合体(RISC)的关键成分Ago2结合。总之,这些结果表明,GAS5在ESCC中作为肿瘤抑制基因发挥作用,并受参与RISC的miR-196a调控。

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