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  • Asakura, Hitoshi  (2)
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  • 1
    Online Resource
    Online Resource
    S. Karger AG ; 2001
    In:  Intervirology Vol. 44, No. 1 ( 2001), p. 21-28
    In: Intervirology, S. Karger AG, Vol. 44, No. 1 ( 2001), p. 21-28
    Abstract: 〈 i 〉 Objective: 〈 /i 〉 The 5′ untranslated region (5′ UTR) of the hepatitis C virus genome is thought to be important for the control of viral gene expression and a likely target for therapeutic interception. A functional role of this viral gene segment was analyzed both in vivo and in vitro. 〈 i 〉 Methods: 〈 /i 〉 Transgenic mice carrying a reporter gene that contains the complete 5′ UTR sequence were made. Cellular protein(s) which associate with the 5′ UTR were analyzed by gel shift analysis and a following affinity purification. 〈 i 〉 Results: 〈 /i 〉 Transgenic mice revealed protein accumulation only in periportal hepatocytes around the portal triad and not in perivenous hepatocytes around the central vein. Gel shift analysis using mouse liver extracts provides further evidence that 〈 i 〉 trans 〈 /i 〉 -acting proteins, which recognize a specific 〈 i 〉 cis 〈 /i 〉 -acting element with the 5′ UTR (an apparent stemmed structure formed by two noncontiguous RNA sequences), are present in adult mice but not in young mice. A similar 5′ UTR RNA-protein complex was also detected with human liver extracts. 〈 i 〉 Conclusion: 〈 /i 〉 The presence of cellular factor(s) which allow HCV 5′ UTR to express in tissue and differentiation state-specific manner was suggested.
    Type of Medium: Online Resource
    ISSN: 0300-5526 , 1423-0100
    RVK:
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2001
    detail.hit.zdb_id: 184545-7
    detail.hit.zdb_id: 1482863-7
    SSG: 12
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  • 2
    In: Journal of Gastroenterology and Hepatology, Wiley, Vol. 16, No. 11 ( 2001-11), p. 1274-1281
    Abstract: The aims of the present study were to determine the occurrence rate of hepatocellular carcinoma (HCC) and to assess the risk factors for the development of HCC in compensated viral liver cirrhosis. Methods: Two hundred and thirty‐nine cirrhotic patients (65 hepatitis B surface antigen (HBsAg) positive, 165 hepatitis C virus (HCV) antibody positive (anti‐HCV), and nine with both HBsAg and anti‐HCV positivity) were studied. The Kaplan–Meier method evaluated by a log–rank test was used to estimate the cumulative probability of HCC development. Independent predictors of HCC development were estimated by using the Cox proportional hazard regression analysis. Results: Dual infection manifested as HBsAg and anti‐HCV positive was the highest risk of HCC. Multivariate analysis indicated that anti‐HCV positive, HBsAg positive, and lactate dehydrogenase were independent predictors of the development of HCC among individuals with viral cirrhosis. In the HBsAg‐positive group, a high‐titer of HBV‐DNA (more than 3.7 log genome equivalents (LGE)/mL) was most predictive of HCC development. In the anti‐HCV‐positive group, male gender and a high‐titer of HCV‐RNA (more than 1.0 Meq/mL) were predictive factors for the development of HCC. Conclusions: Individuals with high viral loads should be monitored for the development of HCC. Clinical efforts at eradicating or reducing the viral load may reduce the risk for HCC.
    Type of Medium: Online Resource
    ISSN: 0815-9319 , 1440-1746
    Language: English
    Publisher: Wiley
    Publication Date: 2001
    detail.hit.zdb_id: 632882-9
    detail.hit.zdb_id: 2006782-3
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