Grant: Operating Grant - PA: Regional Partnership Program - Saskatchewan
University of Saskatchewan
$100,608.00
Molecular mechanisms of hepatitis C virus-associated steatosis
FY 2009-10
Summary
Hepatitis C is a devastating liver disease caused by hepatitis C virus (HCV) infection. A Canadian model has estimated that the economic burden of hepatitis C will increase more than 50% in the next 40 years due primarily to a greater number of patients with more advanced forms of liver diseases caused by HCV infection. Fatty liver disease or steatosis is evident in more than 50% of hepatitis C patients and is a confirmed risk factor for disease progression in hepatitis C. Therefore, we are particularly interested in characterizing how hepatitis C virus causes steatosis. In this proposal, we will provide experimental evidence to demonstrate how hepatitis C virus can modulate lipid synthesis and accumulation through a number of mechanisms in liver cells. This proposal will make a significant contribution to our understanding of steatosis in hepatitis C patients and provide rationale for the development of effective therapeutics to prevent disease progression.
Department
Program
Operating Grant - PA: Regional Partnership Program - Saskatchewan
Recipient
Location
Saskatchewan, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
207272
Name
Liu Qiang
Region
Saskatchewan
Country
Canada
Orgtype
Institution Paid; Research Institution
Partnername
Saskatchewan Health Research Foundation
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Virology & Viral Pathogenesis
Projecttitle
Molecular mechanisms of hepatitis C virus-associated steatosis
Programtype2
Operating Grants
Orgnameinp2
University of Saskatchewan
Cihramount2
$100,608
Cihrequipment2
$0
Programname2
Operating Grant - PA: Regional Partnership Program - Saskatchewan
Keyworddelim
Fatty Liver Disease; Hepatitis C Virus; Signal Transduction Pathway
Abstract
Hepatitis C is a devastating liver disease caused by hepatitis C virus (HCV) infection. A Canadian model has estimated that the economic burden of hepatitis C will increase more than 50% in the next 40 years due primarily to a greater number of patients with more advanced forms of liver diseases caused by HCV infection. Fatty liver disease or steatosis is evident in more than 50% of hepatitis C patients and is a confirmed risk factor for disease progression in hepatitis C. Therefore, we are particularly interested in characterizing how hepatitis C virus causes steatosis. In this proposal, we will provide experimental evidence to demonstrate how hepatitis C virus can modulate lipid synthesis and accumulation through a number of mechanisms in liver cells. This proposal will make a significant contribution to our understanding of steatosis in hepatitis C patients and provide rationale for the development of effective therapeutics to prevent disease progression.
Competitiondate
201003
Approvedterm2
2 yrs 0 mth
Pinamesdelim
Liu, Qiang
Approvedterm
2 ans 0 mois
Cihrcontribution2
SPIR~ $100,608~ $0~