| Literature DB >> 32061951 |
Jin-Long Huang1, Yi-Peng Fu2, Wei Gan1, Gao Liu1, Pei-Yun Zhou1, Cheng Zhou1, Bao-Ye Sun1, Ruo-Yu Guan1, Jian Zhou1, Jia Fan1, Yong Yi3, Shuang-Jian Qiu4.
Abstract
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.Entities:
Keywords: Co-culture; Liver cancer; Metastasis; Tumor microenvironment
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Year: 2020 PMID: 32061951 DOI: 10.1016/j.canlet.2020.02.012
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679