Grant: Operating Grant
McGill University
$683,690.00
Mechanisms governing Hepatitis C virus genome stability and viral RNA accumulation
EF 2013-14
Résumé
Hepatitis C virus (HCV) infection is a global health problem that affects 3% of the world population, including over 300 000 Canadians. HCV-infected individuals typically develop a persistent infection that leads to chronic hepatitis, cirrhosis (fatty liver) and liver cancer. Currently, there is no vaccine available and the current treatment is ineffective in many patients. Thus, there is a pressing need for novel anti-HCV treatments.
To establish an infection, HCV commandeers many different factors in our cells. In healthy cells, small molecules, called microRNAs, restrict how much our genes are expressed. HCV co-opts a liver-specific microRNA and uses it to amplify itself. We have evidence that suggests that the microRNA protects the virus, allowing it to hide from the immune system. The focus of my research is to investigate how HCV uses this microRNA to its own benefit and to identify other human factors that the virus uses to amplify itself in the liver. With this information, we can determine which factors are important for HCV to accumulate in the liver and this will reveal novel antiviral targets.
At present, most therapeutic approaches specifically target the virus. However, HCV is able to mutate to escape the effect of these drugs. Recently, a drug used to sequester this microRNA in HCV-infected patients was demonstrated to have long-lasting suppression of HCV, with no evidence of viral resistance or adverse side effects. Hence, targeting this liver-specific microRNA is a promising antiviral strategy.
Programme
Operating Grant
Bénéficiaire
Emplacement
Quebec, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
305127
Name
Sagan Selena M
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Virology & Viral Pathogenesis
Projecttitle
Mechanisms governing Hepatitis C virus genome stability and viral RNA accumulation
Programtype2
Operating Grants
Orgnameinp2
McGill University
Cihramount2
$683,690
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Click Chemistry; Cross-Linking Immunoprecipitation (Clip); Hepatitis C Virus (Hcv); Individual-Nucleotide Resolution Clip (Iclip); Micrornas; Mir-122; Molecular Virology; Poly-Rc Binding Protein (Pcbp); Rna Binding Protein; Rna Sequencing (Rna-Seq)
Abstract
Hepatitis C virus (HCV) infection is a global health problem that affects 3% of the world population, including over 300 000 Canadians. HCV-infected individuals typically develop a persistent infection that leads to chronic hepatitis, cirrhosis (fatty liver) and liver cancer. Currently, there is no vaccine available and the current treatment is ineffective in many patients. Thus, there is a pressing need for novel anti-HCV treatments.
To establish an infection, HCV commandeers many different factors in our cells. In healthy cells, small molecules, called microRNAs, restrict how much our genes are expressed. HCV co-opts a liver-specific microRNA and uses it to amplify itself. We have evidence that suggests that the microRNA protects the virus, allowing it to hide from the immune system. The focus of my research is to investigate how HCV uses this microRNA to its own benefit and to identify other human factors that the virus uses to amplify itself in the liver. With this information, we can determine which factors are important for HCV to accumulate in the liver and this will reveal novel antiviral targets.
At present, most therapeutic approaches specifically target the virus. However, HCV is able to mutate to escape the effect of these drugs. Recently, a drug used to sequester this microRNA in HCV-infected patients was demonstrated to have long-lasting suppression of HCV, with no evidence of viral resistance or adverse side effects. Hence, targeting this liver-specific microRNA is a promising antiviral strategy.
Competitiondate
201403
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Sagan, Selena M
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $683,690~ $0~