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Grant: Operating Grant

Université de Montréal

$694,425.00

Regulation of senescence and aging by the axis STAT5-SOCS1-p53

FY 2010-11

Summary
Aging is strongly linked to chronic inflammation but the molecular basis of this relationship is poorly understood. Inflammation involves a family of molecules known as cytokines. At the cellular levels cytokine signaling can accelerate the aging process inducing cellular senescence. We have identified a molecular pathway mediating the senescent functions of cytokines. The transcription factor Stat5 which is activated by cytokines, can in turn induce an adaptor protein Socs1 that activates another transcription factor known as p53. The result of activating this pathway is a lost of cellular renewal potential and the secretion of more cytokines. Now we propose to further investigate the molecular properties of these interactions, design assays to find drugs that modulate them and create an animal model to validate our findings in vivo and test for possible pharmacological or nutritional interventions against age-related diseases.
Program
Operating Grant
Location
Quebec, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
209647
Name
Ferbeyre Gerardo
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Aging
Theme2
Biomedical
Prcname2
Biological and Clinical Aspects of Aging
Projecttitle
Regulation of senescence and aging by the axis STAT5-SOCS1-p53
Programtype2
Operating Grants
Orgnameinp2
Université de Montréal
Cihramount2
$694,425
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Aging; Inflammation; P53; Senescence; Stat5; Suppressors Of Cytokine Signaling
Abstract
Aging is strongly linked to chronic inflammation but the molecular basis of this relationship is poorly understood. Inflammation involves a family of molecules known as cytokines. At the cellular levels cytokine signaling can accelerate the aging process inducing cellular senescence. We have identified a molecular pathway mediating the senescent functions of cytokines. The transcription factor Stat5 which is activated by cytokines, can in turn induce an adaptor protein Socs1 that activates another transcription factor known as p53. The result of activating this pathway is a lost of cellular renewal potential and the secretion of more cytokines. Now we propose to further investigate the molecular properties of these interactions, design assays to find drugs that modulate them and create an animal model to validate our findings in vivo and test for possible pharmacological or nutritional interventions against age-related diseases.
Competitiondate
201009
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Ferbeyre, Gerardo
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $694,425~ $0~