| Literature DB >> 25092460 |
Chikako Shibata1, Motoko Ohno1, Motoyuki Otsuka2, Takahiro Kishikawa1, Kaku Goto3, Ryosuke Muroyama3, Naoya Kato3, Takeshi Yoshikawa1, Akemi Takata1, Kazuhiko Koike1.
Abstract
Despite recent progress in the development of direct-acting antivirals against hepatitis C virus (HCV), chronic HCV infection remains an important health burden worldwide. MicroRNA122 (miR122), a liver-specific microRNA (miRNA), positively regulates HCV replication, and systemic application of antisense oligonucleotides against miR122 led to the long-lasting suppression of HCV viremia in human clinical trials. Here, we report that apigenin, a flavonoid and an inhibitor of maturation of a subset of miRNAs, inhibits HCV replication in vitro. Apigenin decreased the expression levels of mature miR122 without significantly affecting cell growth. Because supplementation of synthesized miR122 oligonucleotides or overexpression of constitutively active TRBP blocked these effects, the inhibitory effects of apigenin on HCV replication seemed to be dependent on the reduction of mature miR122 expression levels through inhibition of TRBP phosphorylation. Thus, apigenin intake, either through regular diet or supplements, may decrease HCV replication in chronically infected patients.Entities:
Keywords: HCV; MicroRNA; Polyphenol; Replicon
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Year: 2014 PMID: 25092460 DOI: 10.1016/j.virol.2014.05.024
Source DB: PubMed Journal: Virology ISSN: 0042-6822 Impact factor: 3.616