HNF-4α inhibits hepatocellular carcinoma cell proliferation through mir-122-adam17 pathway

Hepatocellular carcinoma (HCC) is one of the most common human cancers, its prevalence and severity need us to discover novel early diagnostic biomarkers and new therapeutic strategies. MicroRNA-122 is the most abundant microRNA in the liver, and acts as a tumor suppressor and represses HCC developm...

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Veröffentlicht in:PloS one 2020, Vol.15 (3), p.e0230450-e0230450
Hauptverfasser: Yang, Guang, Zhang, Min, Zhao, Yawei, Pan, Yue, Kan, Mujie, Li, Jing, He, Kan, Zhang, Xuewen
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Sprache:eng
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Zusammenfassung:Hepatocellular carcinoma (HCC) is one of the most common human cancers, its prevalence and severity need us to discover novel early diagnostic biomarkers and new therapeutic strategies. MicroRNA-122 is the most abundant microRNA in the liver, and acts as a tumor suppressor and represses HCC development. In our study we showed that HNF-4α and MiR-122 were down-regulated significantly in hepatocellular carcinoma. Over-expression of HNF-4α inhibit hepatocellular carcinoma cells proliferation. And miR-122 is one of the downstream effector of HNF-4α. Up-regulated miR-122 inhibited hepatocellular carcinoma cells proliferation through regulating ADAM17. Collectively, our results suggested that HNF-4α could inhibit hepatocellular carcinoma proliferation with miR-122 being a downstream target of it. And miR-122 would inhibit hepatocellular carcinoma proliferation by regulating ADAM17 signal pathway.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0230450