Taipei Medical University

A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Hung KS
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------>journal_name=Biochem Biophys Res Commun
------>paper_name=Interleukin-10 gene therapy reverses thioacetamide-induced liver fibrosis in mice
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------>fullAbstract=Hepatic fibrosis represents a process of healing and scarring in response to chronic liver injury. Interleukin-10 (IL-10) is a cytokine that downregulates the proinflammatory response and has a modulatory effect on hepatic fibrogenesis. The aim of this study was to investigate whether IL-10 gene therapy possesses anti-hepatic fibrogenesis in mice. Liver fibrosis was induced by long-term thioacetamide administration in mice. Human IL-10 expression plasmid was delivered via electroporation after liver fibrosis established. IL-10 gene therapy reversed hepatic fibrosis and prevented cell apoptosis in a thioacetamide-treated liver. RT-PCR revealed IL-10 gene therapy to reduce liver transforming growth factor-beta1, tumor necrosis factor-alpha, collagen alpha1, cell adhesion molecule, and tissue inhibitors of metalloproteinase mRNA upregulation. Following gene transfer, the activation of alpha-smooth muscle actin and cyclooxygenase-2 was significantly attenuated. In brief, IL-10 gene therapy might be an effective therapeutic reagent for liver fibrosis with potential future clinical applications.
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------>authors2=Lee TH
------>authors3=Chou WY
------>authors4=Wu CL
------>authors5=Cho CL
------>authors6=Lu CN, Jawan B, and Wang CH
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------>authors=Hung KS
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------>updateTitle=Interleukin-10 gene therapy reverses thioacetamide-induced liver fibrosis in mice.
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------>publish_year=2005
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A B C D E F G H I J K L M N O P Q R S T U V W X Y Z