Literature DB >> 26420957

Chronic hepatitis C virus infection and lipoprotein metabolism.

Yoshio Aizawa1, Nobuyoshi Seki1, Tomohisa Nagano1, Hiroshi Abe1.   

Abstract

Hepatitis C virus (HCV) is a hepatotrophic virus and a major cause of chronic liver disease, including hepatocellular carcinoma, worldwide. The life cycle of HCV is closely associated with the metabolism of lipids and lipoproteins. The main function of lipoproteins is transporting lipids throughout the body. Triglycerides, free cholesterol, cholesteryl esters, and phospholipids are the major components of the transported lipids. The pathway of HCV assembly and secretion is closely linked to lipoprotein production and secretion, and the infectivity of HCV particles largely depends on the interaction of lipoproteins. Moreover, HCV entry into hepatocytes is strongly influenced by lipoproteins. The key lipoprotein molecules mediating these interactions are apolipoproteins. Apolipoproteins are amphipathic proteins on the surface of a lipoprotein particle, which help stabilize lipoprotein structure. They perform a key role in lipoprotein metabolism by serving as receptor ligands, enzyme co-factors, and lipid transport carriers. Understanding the association between the life cycle of HCV and lipoprotein metabolism is important because each step of the life cycle of HCV that is associated with lipoprotein metabolism is a potential target for anti-HCV therapy. In this article, we first concisely review the nature of lipoprotein and its metabolism to better understand the complicated interaction of HCV with lipoprotein. Then, we review the outline of the processes of HCV assembly, secretion, and entry into hepatocytes, focusing on the association with lipoproteins. Finally, we discuss the clinical aspects of disturbed lipid/lipoprotein metabolism and the significance of dyslipoproteinemia in chronic HCV infection with regard to abnormal apolipoproteins.

Entities:  

Keywords:  Apolipoprotein; Dyslipoproteinemia; Hepatitis C virus; Lipo-viral particle; Lipoprotein

Mesh:

Substances:

Year:  2015        PMID: 26420957      PMCID: PMC4579877          DOI: 10.3748/wjg.v21.i36.10299

Source DB:  PubMed          Journal:  World J Gastroenterol        ISSN: 1007-9327            Impact factor:   5.742


  133 in total

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Journal:  Dig Liver Dis       Date:  2014-05-29       Impact factor: 4.088

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Journal:  PLoS One       Date:  2014-03-19       Impact factor: 3.240

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2.  Hepatitis C Virus Alters Macrophage Cholesterol Metabolism Through Interaction with Scavenger Receptors.

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Review 3.  Hepatitis C virus-apolipoprotein interactions: molecular mechanisms and clinical impact.

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4.  Hepatitis B virus inhibits apolipoprotein A5 expression through its core gene.

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Journal:  Lipids Health Dis       Date:  2016-10-10       Impact factor: 3.876

5.  Impact of interferon-free antivirus therapy on lipid profiles in patients with chronic hepatitis C genotype 1b.

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Review 6.  Hepatitis C Virus Infection Induces Autophagy as a Prosurvival Mechanism to Alleviate Hepatic ER-Stress Response.

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8.  Rapid Changes in Serum Lipid Profiles during Combination Therapy with Daclatasvir and Asunaprevir in Patients Infected with Hepatitis C Virus Genotype 1b.

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9.  Glycogen synthase kinase 3β inhibitors prevent hepatitis C virus release/assembly through perturbation of lipid metabolism.

Authors:  Mohammed A Sarhan; Mohamed S Abdel-Hakeem; Andrew L Mason; D Lorne Tyrrell; Michael Houghton
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Review 10.  Carboxylesterases in lipid metabolism: from mouse to human.

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