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Grant: Project Grant

Université de Sherbrooke

$803,250.00

A critical role for DUal Specificity Phosphatase 4 in intestinal oncogenesis?

FY 2018-19

Summary
For men and women combined, colorectal cancer is a leading cause of cancer-related deaths in Canada. Mechanisms underlying colorectal cancer development are complex and heterogeneous. Mutations in KRAS and BRAF genes are found in up to 50% of these cancers. In the cell, RAS and RAF proteins are two major players in the MAP kinase pathway, which is a chain of proteins that communicates a signal from a receptor on the surface of the cell to the DNA in the nucleus. Recent research in colorectal cancer cells supports the possibility that a significant subset of these cancers will be responsive to inhibitors of this pathway. However, the MAP Kinase pathway is not a simple linear pathway, with a multitude of positive and negative regulatory components operating at all levels of the cascade. The focus of our research is to analyze the contribution of DUSP4, an inhibitor of MAP Kinase pathway, in intestinal tumour development. Our long-term is to determine if DUSP4 can be used clinically as a biomarker or therapeutic target for colorectal cancer.
Program
Project Grant
Location
Quebec, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
401011
Name
Rivard Nathalie
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Molecular & Cellular Biology of Cancer
Projecttitle
A critical role for DUal Specificity Phosphatase 4 in intestinal oncogenesis?
Programtype2
Operating Grants
Orgnameinp2
Université de Sherbrooke
Cihramount2
$803,250
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Apc; Braf; Cell Signalling; Colorectal Cancer; Dual Specificity Phosphatase; Intestinal Epithelium; Kras; Map Kinases
Abstract
For men and women combined, colorectal cancer is a leading cause of cancer-related deaths in Canada. Mechanisms underlying colorectal cancer development are complex and heterogeneous. Mutations in KRAS and BRAF genes are found in up to 50% of these cancers. In the cell, RAS and RAF proteins are two major players in the MAP kinase pathway, which is a chain of proteins that communicates a signal from a receptor on the surface of the cell to the DNA in the nucleus. Recent research in colorectal cancer cells supports the possibility that a significant subset of these cancers will be responsive to inhibitors of this pathway. However, the MAP Kinase pathway is not a simple linear pathway, with a multitude of positive and negative regulatory components operating at all levels of the cascade. The focus of our research is to analyze the contribution of DUSP4, an inhibitor of MAP Kinase pathway, in intestinal tumour development. Our long-term is to determine if DUSP4 can be used clinically as a biomarker or therapeutic target for colorectal cancer.
Competitiondate
201903
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Rivard, Nathalie
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $803,250~ $0~