Wnt信号通路
癌症研究
基因敲除
下调和上调
小RNA
连环素
癌变
肝星状细胞
肝细胞癌
生物
连环蛋白
上皮-间质转换
化学
医学
细胞生物学
细胞培养
内科学
信号转导
基因
内分泌学
癌症
遗传学
作者
Jinlong Huang,Yi‐Peng Fu,Wei Gan,Gao Liu,Pei‐Yun Zhou,Cheng Zhou,Bao‐Ye Sun,Ruo‐Yu Guan,Jian Zhou,Jia Fan,Yong Yi,Shuang‐Jian Qiu
出处
期刊:Cancer Letters
[Elsevier BV]
日期:2020-02-13
卷期号:476: 140-151
被引量:65
标识
DOI:10.1016/j.canlet.2020.02.012
摘要
Hepatic stellate cells (HSCs) play vital roles in tumorigenesis and progression of hepatocellular carcinoma (HCC). However, there remains a lack of high-throughput studies on gene expression alterations in HCC cells in response to direct interactions with HSCs. In this study, we established a direct co-culture model of HSCs and HCC cells. We found that the expression of a set of miRNAs, most notably miR-1246, was triggered by HSCs. RORα was confirmed as the target gene of miR-1246. Either overexpression of miR-1246 or knockdown of RORα enhanced the proliferation, invasiveness, and metastatic capability of HCC both in vitro and in vivo, through Wnt/β-catenin pathway activation and promotion of epithelial-mesenchymal transition (EMT). Moreover, upregulation of miR-1246 and repression of RORα were prominent features of aggressive clinical HCC. The miR-1246-RORα-Wnt/β-catenin axis is a novel pathway through which HSCs accelerate HCC progression.
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