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Grant: Operating Grant - PA: Regional Partnership Program - Newfoundland and Labrador

Memorial University of Newfoundland

$167,329.00

Mechanisms of Ras-dependent oncolysis

FY 2011-12

Summary
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 believe that the Ras/MEK pathway inhibits function of a cellular protein known as 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.
Program
Operating Grant - PA: Regional Partnership Program - Newfoundland and Labrador
Location
Newfoundland and Labrador, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
259631
Name
Hirasawa Kensuke
Region
Newfoundland and Labrador
Country
Canada
Orgtype
Institution Paid; Research Institution
Partnername
Newfoundland and Labrador Research & Development Corp.
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Virology & Viral Pathogenesis
Projecttitle
Mechanisms of Ras-dependent oncolysis
Programtype2
Operating Grants
Orgnameinp2
Memorial University of Newfoundland
Cihramount2
$167,329
Cihrequipment2
$0
Programname2
Operating Grant - PA: Regional Partnership Program - Newfoundland and Labrador
Keyworddelim
Cancer Therapy; Cell Signaling; Interferon (Ifn); Irf1; Oncolytic Virus; Ras/Mek; Transcription; 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 believe that the Ras/MEK pathway inhibits function of a cellular protein known as 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.
Competitiondate
201203
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Hirasawa, Kensuke
Approvedterm
3 ans 0 mois
Cihrcontribution2
SPIR~ $167,329~ $0~
Memorial University of Newfoundland - $167,329 Grant… | Canada Spends