Regulation of transforming growth factor-β1 expression by the hepatitis B virus(HBV) X transactivator : role in HBV pathogenesis

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dc.contributor.authorYoung Do Yoo-
dc.contributor.authorH Ueda-
dc.contributor.authorKeunchil Park-
dc.contributor.authorK C Flanders-
dc.contributor.authorYoung Ik Lee-
dc.contributor.authorG Jay-
dc.contributor.authorSeong-Jin Kim-
dc.date.accessioned2017-04-19T08:45:14Z-
dc.date.available2017-04-19T08:45:14Z-
dc.date.issued1996-
dc.identifier.issn0021-9738-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/3676-
dc.description.abstractTGF-β1 has been implicated in the pathogenesis of liver disease. The high frequency of detection of the hepatitis B virus X (HBx) antigen in liver cells from patients with chronic hepatitis, cirrhosis, and liver cancer suggested that expression of HBx and TGF-β1 may be associated. To test this possibility, we examined the expression of TGF-β1 in the liver of transgenic mice expressing the HBx gene. We show that the patterns of expression of TGF-β1 and Hbx protein are similar in these mice and that HBx activates transcription of the TGF-β1 gene in transfected hepatoma cells. The cis-acting element within the TGF-β1 gene that is responsive to regulation by Hbx is the binding site for the Egr family of transcription factors. We further show that the Egr-1 protein associates with the HBx protein, allowing HBx to participate in the transcriptional regulation of immediate-early genes. Our results suggest that expression of Hbx might induce expression of TGF-β1 in the early stages of infection and raise the possibility that TGF-ßl may play a role in hepatitis B virus pathogenesis.-
dc.publisherAmer Soc Clinical Investigation Inc-
dc.titleRegulation of transforming growth factor-β1 expression by the hepatitis B virus(HBV) X transactivator : role in HBV pathogenesis-
dc.title.alternativeRegulation of transforming growth factor-β1 expression by the hepatitis B virus(HBV) X transactivator : role in HBV pathogenesis-
dc.typeArticle-
dc.citation.titleJournal of Clinical Investigation-
dc.citation.number2-
dc.citation.endPage395-
dc.citation.startPage388-
dc.citation.volume97-
dc.contributor.affiliatedAuthorYoung Ik Lee-
dc.contributor.alternativeName유영도-
dc.contributor.alternativeNameUeda-
dc.contributor.alternativeName박근칠-
dc.contributor.alternativeNameFlanders-
dc.contributor.alternativeName이영익-
dc.contributor.alternativeNameJay-
dc.contributor.alternativeName김성진-
dc.identifier.bibliographicCitationJournal of Clinical Investigation, vol. 97, no. 2, pp. 388-395-
dc.identifier.doi10.1172/JCI118427-
dc.subject.keywordhepatitis B virus-
dc.subject.keywordhepatocellular carcinoma-
dc.subject.keywordimmunohistochemistry-
dc.subject.keywordTGF-β1-
dc.subject.keywordtranscription-
dc.subject.localHepatitis B Virus-
dc.subject.localHepatitis B virus-
dc.subject.localHepatitis B virus (HBV)-
dc.subject.localhepatitis B Virus (HBV)-
dc.subject.localhepatitis B virus-
dc.subject.localhepatitis B virus (HBV)-
dc.subject.localHepatocellular carcinoma-
dc.subject.localHepatocellular carcinoma (HCC)-
dc.subject.localHepatocellular carcinomas-
dc.subject.localhepatocellular carcinoma-
dc.subject.localhepatocellular carcinoma (HCC)-
dc.subject.localImmunohistochemistry-
dc.subject.localimmunohistochemistry-
dc.subject.localimmunohistochimistry-
dc.subject.localTGF-β1-
dc.subject.localTGFβ-1-
dc.subject.localTranscription-
dc.subject.localtranscription-
dc.description.journalClassY-
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