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Hsa_circ_0009910通过促进骨肉瘤中miR-449a的靶标IL6R的表达来促进肿瘤发生。

Hsa_circ_0009910 promotes carcinogenesis by promoting the expression of miR-449a target IL6R in osteosarcoma.

作者信息

Deng Nian, Li Longyang, Gao Jinghao, Zhou Jun, Wang Yan, Wang Chao, Liu Yong

机构信息

Department of Orthopaedics, Qingdao Hiser Medical Center, Qingdao, China.

Department of Orthopedic Surgery, The Affiliated Hospital of Qingdao University, Qingdao, China.

出版信息

Biochem Biophys Res Commun. 2018 Jan 1;495(1):189-196. doi: 10.1016/j.bbrc.2017.11.028. Epub 2017 Nov 5.

Abstract

Circular RNAs (circRNAs) have recently shown capabilities as gene regulators in mammals. Some of them interact with microRNAs (miRNAs) and function as sponges to affect related miRNAs' activities. In this study, the molecular function of circRNA_0009910 and its potential downstream miRNA targets were explored. The expression levels of hsa_circ_0009910 were found to be overexpressed in osteosarcoma (OS) cells. Knockdown of circ_0009910 induced cell proliferation inhibition, cell cycle arrest, and apoptosis in OS cells. The target miRNA was predicted to be miR-449a, whose expression was downregulated in OS cells. Inhibition of miR-449a abolished the effect of circ_0009910 knockdown on cell growth and apoptosis. The expression of miR-449a were found to be negatively correlated with that of circ_0009910 in OS tissues. Direct interaction of circ_0009910 and miR-449a was confirmed through dual-luciferase assays. Moreover, IL6R was predicted as a potential target of miR-449a. Overexpression of miR-449a decreased the mRNA and protein levels of IL6R. Restoration of IL6R impaired the miR-449a induced inhibition of cell proliferation, cell cycle arrest, and apoptosis. The mRNA expression of IL6R was inversely correlated with miR-449a in OS tissues. In addition, JAK1/STAT3 signaling pathway was regulated by circ_0009910/miR-449a/IL6R axis. Taken together, we suggested that circ_0009910 acted as a sponge of miR-449a and upregulated miR-449a functional target IL6R, thereby contributed to carcinogenesis of OS.

摘要

环状RNA(circRNAs)最近在哺乳动物中展现出作为基因调控因子的能力。其中一些与微小RNA(miRNAs)相互作用,并作为海绵发挥作用以影响相关miRNAs的活性。在本研究中,探索了circRNA_0009910的分子功能及其潜在的下游miRNA靶点。发现hsa_circ_0009910在骨肉瘤(OS)细胞中过表达。敲低circ_0009910可诱导OS细胞增殖抑制、细胞周期停滞和凋亡。预测靶miRNA为miR-449a,其在OS细胞中的表达下调。抑制miR-449a可消除circ_0009910敲低对细胞生长和凋亡的影响。发现在OS组织中miR-449a的表达与circ_0009910的表达呈负相关。通过双荧光素酶测定证实了circ_0009910与miR-449a的直接相互作用。此外,预测IL6R是miR-449a的潜在靶点。miR-449a的过表达降低了IL6R的mRNA和蛋白水平。IL6R的恢复削弱了miR-449a诱导的细胞增殖抑制、细胞周期停滞和凋亡。在OS组织中IL6R的mRNA表达与miR-449a呈负相关。此外,circ_0009910/miR-449a/IL6R轴调节JAK1/STAT3信号通路。综上所述,我们认为circ_0009910作为miR-449a的海绵,上调了miR-449a的功能靶点IL6R,从而促进了OS的致癌作用。

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