Grant: Project Grant
Memorial University of Newfoundland
$573,750.00
Regulation of antiviral responses by Ras/MEK
EF 2016-17
Résumé
Oncolytic viruses are engineered or naturally occurring viruses that replicate in cancer cells,
but not in normal cells. They have become a focus of attention for cancer therapy in recent
years as clinical studies have shown them to be quite promising. However, the biochemical
mechanisms of their tumor selectivity still remain to be studied. In this proposal, we will
investigate how one of the oncogenic cell signaling pathways, Ras/MEK, promotes the
replication of certain oncolytic viruses in cancer cells. We will investigate how the Ras/MEK
pathway inhibits function of interferon regulatory factor (IRF)-1, which is known to block viral
replication, resulting in efficient replication of oncolytic viruses in cancer cells. Our study will
provide a novel insight into the molecular mechanisms of viral oncolysis as well as the future
development of new oncolytic viruses with improved efficacy and safety in treating cancer.
Programme
Project Grant
Bénéficiaire
Emplacement
Newfoundland and Labrador, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
355606
Name
Hirasawa Kensuke
Region
Newfoundland and Labrador
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Project Grant Competition
Projecttitle
Regulation of antiviral responses by Ras/MEK
Programtype2
Operating Grants
Orgnameinp2
Memorial University of Newfoundland
Cihramount2
$573,750
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Cancer Therapy; Irf1; Oncolytic Virus; Ras/Mek; Sumoylation; Virology; Virus Infection
Abstract
Oncolytic viruses are engineered or naturally occurring viruses that replicate in cancer cells,
but not in normal cells. They have become a focus of attention for cancer therapy in recent
years as clinical studies have shown them to be quite promising. However, the biochemical
mechanisms of their tumor selectivity still remain to be studied. In this proposal, we will
investigate how one of the oncogenic cell signaling pathways, Ras/MEK, promotes the
replication of certain oncolytic viruses in cancer cells. We will investigate how the Ras/MEK
pathway inhibits function of interferon regulatory factor (IRF)-1, which is known to block viral
replication, resulting in efficient replication of oncolytic viruses in cancer cells. Our study will
provide a novel insight into the molecular mechanisms of viral oncolysis as well as the future
development of new oncolytic viruses with improved efficacy and safety in treating cancer.
Competitiondate
201610
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Hirasawa, Kensuke
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $573,750~ $0~