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
肝癌
肝细胞癌
生物
细胞生长
连环蛋白
干瘪的
环状RNA
肿瘤科
河马信号通路
上皮-间质转换
基因沉默
化学
细胞周期蛋白D1
医学
细胞生物学
细胞培养
内科学
信号转导
基因
癌症
生物化学
遗传学
作者
Huang Ji,Yi‐Peng Fu,Wei Gan,Gao Liu,Pei‐Yun Zhou,Cheng Zhou,Bao-Ye Sun,Ruijuan Guan,Jian Zhou,Jian‐Gao Fan,Yong Yi,Shuang–Jian Qiu
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI