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Grant: Operating Grant: Industry-partnered Collaborative Research - Other Partner

Research Institute of the McGill University Health Centre

$60,000.00

Role of endoglin in aberrant TGF-beta signaling in scleroderma

EF 2010-11

Résumé
Scleroderma or systemic sclerosis (SSc) is a chronic connective tissue disease that is characterized by defective immune system function, blood vessel damage and scarring (fibrosis) of the skin and internal organs. Fibrosis is a prominent feature of SSc and involves excessive production of collagen and other extracellular matrix (ECM) proteins leading to disruption of the tissue structure and eventually organ failure. Fibrosis has a significant impact on the quality of life and is the main cause of death in SSc. Transforming growth factor-beta(TGF-beta) is produced by most cells of the body and is important for the maintenance of healthy tissues. Abnormal TGF-beta action is thought to be involved in many fibrotic disorders including SSc. Our research goals are to understand the biology of TGF-beta in human skin cells and to uncover how deregulated TGF-beta action is involved in SSc fibrosis. The proposed research may lead to the development of new therapies for the treatment of this disease.
Programme
Operating Grant: Industry-partnered Collaborative Research - Other Partner
Emplacement
Quebec, Canada
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
221584
Name
Philip Anie
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Musculoskeletal Health and Arthritis
Theme2
Biomedical
Prcname2
Industry Partnered Collaborative Research
Projecttitle
Role of endoglin in aberrant TGF-beta signaling in scleroderma
Programtype2
Operating Grants
Orgnameinp2
Research Institute of the McGill University Health Centre
Cihramount2
$60,000
Cihrequipment2
$0
Programname2
Operating Grant: Industry-partnered Collaborative Research - Other Partner
Keyworddelim
Alk1; Alk5; Bleomycin; Endoglin; Fibrosis; Map Kinases; Mouse Model; Receptors; Scleroderma; Tgf-Beta
Abstract
Scleroderma or systemic sclerosis (SSc) is a chronic connective tissue disease that is characterized by defective immune system function, blood vessel damage and scarring (fibrosis) of the skin and internal organs. Fibrosis is a prominent feature of SSc and involves excessive production of collagen and other extracellular matrix (ECM) proteins leading to disruption of the tissue structure and eventually organ failure. Fibrosis has a significant impact on the quality of life and is the main cause of death in SSc. Transforming growth factor-beta(TGF-beta) is produced by most cells of the body and is important for the maintenance of healthy tissues. Abnormal TGF-beta action is thought to be involved in many fibrotic disorders including SSc. Our research goals are to understand the biology of TGF-beta in human skin cells and to uncover how deregulated TGF-beta action is involved in SSc fibrosis. The proposed research may lead to the development of new therapies for the treatment of this disease.
Competitiondate
201009
Approvedterm2
2 yrs 0 mth
Pinamesdelim
Philip, Anie
Approvedterm
2 ans 0 mois
Cihrcontribution2
Knowledge Translation Branch~ $60,000~ $0~