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Synergistic inhibition of hepatitis C virus infection by a novel microtubule inhibitor in combination with daclatasvir.
Zhang, Huijun; Zhang, Xing-Quan; Huang, Lina S; Fang, Xiong; Khan, Mohsin; Xu, Yan; An, Jing; Schooley, Robert T; Huang, Ziwei.
Afiliação
  • Zhang H; Division of Infectious Diseases and Global Public Health, Department of Medicine, School of Medicine, University of California at San Diego, La Jolla, 92093, California, USA.
  • Zhang XQ; School of Life and Health Sciences, The Chinese University of Hong Kong, Shenzhen, 518172, China.
  • Huang LS; School of Life Sciences, Tsinghua University, Beijing, 100084, China.
  • Fang X; Division of Infectious Diseases and Global Public Health, Department of Medicine, School of Medicine, University of California at San Diego, La Jolla, 92093, California, USA.
  • Khan M; Division of Infectious Diseases and Global Public Health, Department of Medicine, School of Medicine, University of California at San Diego, La Jolla, 92093, California, USA.
  • Xu Y; School of Life Sciences, Tsinghua University, Beijing, 100084, China.
  • An J; Division of Infectious Diseases and Global Public Health, Department of Medicine, School of Medicine, University of California at San Diego, La Jolla, 92093, California, USA.
  • Schooley RT; School of Life and Health Sciences, The Chinese University of Hong Kong, Shenzhen, 518172, China.
  • Huang Z; Division of Infectious Diseases and Global Public Health, Department of Medicine, School of Medicine, University of California at San Diego, La Jolla, 92093, California, USA.
Biochem Biophys Rep ; 30: 101283, 2022 Jul.
Article em En | MEDLINE | ID: mdl-35647321
ABSTRACT
Even though substantial progress has been made in the treatment of hepatitis C virus (HCV) infection, viral resistance and relapse still occur in some patients and additional therapeutic approaches may ultimately be needed should viral resistance become more prevalent. Microtubules play important roles in several HCV life cycle events, including cell attachment, entry, cellular transportation, morphogenesis and progeny secretion steps. Therefore, it was hypothesized that microtubular inhibition might be a novel approach for the treatment of HCV infection. Here, the inhibitory effects of our recently developed microtubule inhibitors were studied in the HCV replicon luciferase reporter system and the infectious system. In addition, the combination responses of microtubule inhibitors with daclatasvir, which is a clinically used HCV NS5A inhibitor, were also evaluated. Our results indicated that microtubule targeting had activity against HCV replication and showed synergistic effect with a current clinical drug.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Biochem Biophys Rep Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Biochem Biophys Rep Ano de publicação: 2022 Tipo de documento: Article