Grant: Project Grant
McGill University
$757,350.00
A novel mechanism for GPCR-dependent activation of BRD4
FY 2019-20
Summary
Cells are constantly responding to signals from their surrounding environment. These signals influence cellular behavior in many ways: they can promote or arrest growth and division, stimulate migration, alter electrical properties, or lead to programmed cell death. Cells respond to these signals by virtue of receptors on their surface, which, when engaged, trigger cascades of molecular events inside the cell; in disease these pathways are abnormally wired or abnormally active. In many cases these pathways culminate in changes in gene expression, but we still do not fully understand the molecular events that translate signals into effects on genes. In this project we will characterize a novel mechanism we have discovered for signal-dependent regulation of a protein called BRD4. BRD4 is a key regulator of gene expression and is abnormally active in a wide range of diseases including cancer and heart disease. By learning more about how BRD4 activity is turned on and off, we hope to uncover new therapeutic strategies for modulating BRD4 activity in disease states, as well as new clinical settings in which BRD4 inhibition may be beneficial.
Department
Program
Project Grant
Recipient
Location
Quebec, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
419946
Name
Tanny Jason C
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Genetics
Theme2
Biomedical
Prcname2
Cell Biology - Disease
Projecttitle
A novel mechanism for GPCR-dependent activation of BRD4
Programtype2
Operating Grants
Orgnameinp2
McGill University
Cihramount2
$757,350
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Brd4; Cardiac Hypertrophy; G-Protein Coupled Receptor; Protein Kinase A; Transcription Elongation
Abstract
Cells are constantly responding to signals from their surrounding environment. These signals influence cellular behavior in many ways: they can promote or arrest growth and division, stimulate migration, alter electrical properties, or lead to programmed cell death. Cells respond to these signals by virtue of receptors on their surface, which, when engaged, trigger cascades of molecular events inside the cell; in disease these pathways are abnormally wired or abnormally active. In many cases these pathways culminate in changes in gene expression, but we still do not fully understand the molecular events that translate signals into effects on genes. In this project we will characterize a novel mechanism we have discovered for signal-dependent regulation of a protein called BRD4. BRD4 is a key regulator of gene expression and is abnormally active in a wide range of diseases including cancer and heart disease. By learning more about how BRD4 activity is turned on and off, we hope to uncover new therapeutic strategies for modulating BRD4 activity in disease states, as well as new clinical settings in which BRD4 inhibition may be beneficial.
Competitiondate
202003
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Tanny, Jason C
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $757,350~ $0~