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Research Article Free access | 10.1172/JCI118427

Regulation of transforming growth factor-beta 1 expression by the hepatitis B virus (HBV) X transactivator. Role in HBV pathogenesis.

Y D Yoo, H Ueda, K Park, K C Flanders, Y I Lee, G Jay, and S J Kim

Laboratory of Chemoprevention, National Cancer Institute, Bethesda, Maryland 20892, USA.

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Laboratory of Chemoprevention, National Cancer Institute, Bethesda, Maryland 20892, USA.

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Laboratory of Chemoprevention, National Cancer Institute, Bethesda, Maryland 20892, USA.

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Laboratory of Chemoprevention, National Cancer Institute, Bethesda, Maryland 20892, USA.

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Laboratory of Chemoprevention, National Cancer Institute, Bethesda, Maryland 20892, USA.

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Laboratory of Chemoprevention, National Cancer Institute, Bethesda, Maryland 20892, USA.

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Laboratory of Chemoprevention, National Cancer Institute, Bethesda, Maryland 20892, USA.

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Published January 15, 1996 - More info

Published in Volume 97, Issue 2 on January 15, 1996
J Clin Invest. 1996;97(2):388–395. https://doi.org/10.1172/JCI118427.
© 1996 The American Society for Clinical Investigation
Published January 15, 1996 - Version history
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Abstract

TGF-beta 1 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-beta 1 may be associated. To test this possibility, we examined the expression of TGF-beta 1 in the liver of transgenic mice expressing the HBx gene. We show that the patterns of expression of TGF-beta 1 and Hbx protein are similar in these mice and that HBx activates transcription of the TGF-beta 1 gene in transfected hepatoma cells. The cis-acting element within the TGF-beta 1 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-beta 1 in the early stages of infection and raise the possibility that TGF-beta 1 may play a role in hepatitis B virus pathogenesis.

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