期刊
ANTIVIRAL RESEARCH
卷 145, 期 -, 页码 123-130出版社
ELSEVIER
DOI: 10.1016/j.antiviral.2017.07.018
关键词
Hepatitis C virus; Cinnamic acid; STAT3; Reactive oxygen species
资金
- Research Programs from the Japan Agency for Medical Research and Development [16fk0210109h1301, 16fk0210106h0001]
- JSPS KAKENHI [JP 15K08493]
- Yakult Co. Ltd.
- Grants-in-Aid for Scientific Research [15K08493] Funding Source: KAKEN
Several cinnamic acid derivatives have been reported to exhibit antiviral activity. In this study, we prepared 17 synthetic cinnamic acid derivatives and screened them to identify an effective antiviral compound against hepatitis C virus (HCV). Compound 6, one of two hit compounds, suppressed the viral replications of genotypes lb, 2a, 3a, and 4a with EC50 values of 1.5-8.1 mu M and SI values of 16.2-94.2. The effect of compound 6 on the phosphorylation of Tyr(705) in signal transducer and activator of transcription 3 (STAT3) was investigated because a cinnamic acid derivative AG490 was reported to suppress HCV replication and the activity of Janus kinase (JAM) 2. Compound 6 potently suppressed HCV replication, but it did not inhibit the JAK1/2-dependent phosphorylation of STAT3 Tyr(705) at the same concentration. Furthermore, a pan JAM inhibitor tofacitinib potently impaired phosphorylation of STAT3 Tyr (705), but it did not inhibit HCV replication in the replicon cells and HCV-infected cells at the same concentration, supporting the notion that the phosphorylated state of STAT3 Tyr(705) is not necessarily correlated with HCV replication. The production of reactive oxygen species (ROS) was induced by treatment with compound 6, whereas N-acetyl-cysteine restored HCV replication and impaired ROS production in the replicon cells treated with compound 6. These data suggest that compound 6 inhibits HCV replication via the induction of oxidative stress. (C) 2017 Elsevier B.V. All rights reserved.
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