4.6 Article

miR-122-induced down-regulation of HO-1 negatively affects miR-122-mediated suppression of HBV

Journal

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbrc.2010.07.021

Keywords

miR-122; Hepatitis B virus; Heme oxgenase-1; Cobalt protoporphyrin

Funding

  1. National High Technology Research and Development Program of China [2006AA02A241]
  2. Major State Basic Research Development Program of China [2007CB512802]
  3. Key Projects in the National Science & Technology Program of Eleventh Five-year Plan [2008ZX10002-005-3]

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As the most abundant liver-specific microRNA (miRNA), miR-122 has been extensively studied for its role in the regulation of lipid metabolism, hepatocarcinogenesis and hepatitis C virus (HCV) replication, but little is known regarding its role in the replication of Hepatitis B virus (HBV), a highly prevalent hepatotropic virus that can cause life-threatening complications. In this study we examined the effects of antisense inhibition of miR-122 and transfection of a miR-122 mimic on HBV expression in hepatoma cells. The over-expression of miR-122 inhibited HBV expression, whereas the depletion of endogenous miR-122 resulted in increased production of HBV in transfected cells. We further found that the down-regulation of Heme oxygenase-1 (HO-1) by miR-122 plays a negative role in the miR-122-mediated inhibition of viral expression. Our study demonstrates the anti-HBV activity of miR-122, suggesting that therapies that increase miR-122 and HO-1 may be an effective strategy to limit HBV replication. (C) 2010 Elsevier Inc. All rights reserved.

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