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微小RNA-146a通过靶向锌指蛋白3/糖原合成酶激酶-3β/β-连环蛋白信号通路促进骨肉瘤细胞生长。

miR-146a promotes growth of osteosarcoma cells by targeting ZNRF3/GSK-3β/β-catenin signaling pathway.

作者信息

Zhou Chun, Jiang Chang-Qing, Zong Zhen, Lin Jia-Chen, Lao Li-Feng

机构信息

Department of Orthopaedic Surgery, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.

出版信息

Oncotarget. 2017 Jul 19;8(43):74276-74286. doi: 10.18632/oncotarget.19395. eCollection 2017 Sep 26.

DOI:10.18632/oncotarget.19395
PMID:29088784
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5650339/
Abstract

MicroRNA-146a-5p (miR-146a) functions as a tumor suppressor or oncogene involved in multiple biological processes. But, the underlying molecular mechanisms by which miR-146a contributes to osteosarcoma (OS) remain unclear. The correlation of miR-146a expression with clinicopathologic characteristics and prognosis of OS patients was analyzed by Kaplan-Meier and Cox regression analysis. Cell growth and was assessed by MTT, cell colony formation and animal models. The target of miR-146a was identified by bioinformatics software and gene luciferase reporter. As a result, miR-146a expression was substantially elevated in OS tissues and was positively associated with the tumor size (=0.001) and recurrence (=0.027) of OS patients. Moreover, knockdown of miR-146a suppressed cell proliferation and colony formation and . In addition, zinc and ring finger 3 (ZNRF3) was identified as a direct target of miR-146a in OS cells, and was negatively correlated with miR-146a expression in OS tissues. Overexpression of ZNRF3 inhibited cell growth and rescued the tumor-promoting role of miR-146a via inhibition of GSK-3β/β-catenin signaling pathway. Taken together, miR-146a may function as an oncogene in OS cells by targeting ZNRF3/GSK-3β/β-catenin signaling pathway, and represent a promising biomarker for OS patients.

摘要

微小RNA-146a-5p(miR-146a)作为一种抑癌基因或癌基因参与多种生物学过程。但是,miR-146a促成骨肉瘤(OS)的潜在分子机制仍不清楚。通过Kaplan-Meier和Cox回归分析,分析了miR-146a表达与OS患者临床病理特征及预后的相关性。通过MTT、细胞集落形成和动物模型评估细胞生长情况。通过生物信息学软件和基因荧光素酶报告基因鉴定miR-146a的靶标。结果显示,miR-146a在OS组织中的表达显著升高,且与OS患者的肿瘤大小(P=0.001)和复发(P=0.027)呈正相关。此外,敲低miR-146a可抑制细胞增殖和集落形成。另外,锌指蛋白3(ZNRF3)被鉴定为OS细胞中miR-146a的直接靶标,且在OS组织中与miR-146a表达呈负相关。ZNRF3的过表达抑制细胞生长,并通过抑制GSK-3β/β-连环蛋白信号通路挽救miR-146a的促肿瘤作用。综上所述,miR-146a可能通过靶向ZNRF3/GSK-3β/β-连环蛋白信号通路在OS细胞中发挥癌基因功能,并有望成为OS患者的生物标志物。

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