Hydroxyurea as an inhibitor of hepatitis C virus RNA replication

Hepatitis C virus (HCV) is the main causative agent of chronic liver disease, which may develop into liver cirrhosis and hepatocellular carcinoma. By using a recently developed reporter assay system in which genome-length HCV RNA replicates efficiently, we found that hydroxyurea (HU), a DNA synthesi...

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Bibliographic Details
Published inArchives of virology Vol. 155; no. 4; pp. 601 - 605
Main Authors Nozaki, Akito, Morimoto, Manabu, Kondo, Masaaki, Oshima, Takashi, Numata, Kazushi, Fujisawa, Shin, Kaneko, Takeshi, Miyajima, Eiji, Morita, Satoshi, Mori, Kyoko, Ikeda, Masanori, Kato, Nobuyuki, Tanaka, Katsuaki
Format Journal Article
LanguageEnglish
Published Vienna Vienna : Springer Vienna 01.04.2010
Springer Vienna
Springer
Springer Nature B.V
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Summary:Hepatitis C virus (HCV) is the main causative agent of chronic liver disease, which may develop into liver cirrhosis and hepatocellular carcinoma. By using a recently developed reporter assay system in which genome-length HCV RNA replicates efficiently, we found that hydroxyurea (HU), a DNA synthesis inhibitor, inhibited HCV RNA replication. Moreover, we demonstrated that the anti-HCV activity of the combination of IFN-alpha and HU was higher than that of IFN-alpha alone. These results suggest that HU may be an effective anti-HCV reagent that can be used not only singly but also in combination with IFN-alpha to treat chronic hepatitis C.
Bibliography:http://dx.doi.org/10.1007/s00705-010-0624-1
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ISSN:0304-8608
1432-8798
DOI:10.1007/s00705-010-0624-1