Grant: Operating Grant
Centre hospitalier de l'Université de Montréal (CHUM)
$612,420.00
Bcl-xL regulation and function during G2 and mitotic spindle assembly checkpoints
EF 2008-09
Résumé
The Bcl-2 family of proteins stands among the most crucial regulators of cell death (apoptosis) and performs vital function in deciding whether a cancer cell will live or die after cancer chemotherapy and radiotherapy. In addition, recent studies reveal
that members of the family also interface with cell cycle progression and DNA repair pathways, effects that are generally distinct from their functions in apoptosis. This study will focus on one member of the Bcl-2 family, and further analyse the mechanisms by
which Bcl-xL plays roles during the cell cycle checkpoints. Many efforts are already being pursued to develop new drugs targeting anti-apoptotic bcl-2 and cell cycle regulatory family members, with the ultimate goal of improving or developing alternative therapeutic protocols for cancer therapy. Thus, it is important to explore how these key regulatory molecules interface together to improve our understanding for potential clinical use of these novel cancer chemotherapy molecules.
Programme
Operating Grant
Emplacement
Quebec, Canada
Type de bénéficiaire
Not-for-profit organization or charity
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
180803
Name
Bertrand Richard
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Cancer Biology & Therapeutics
Projecttitle
Bcl-xL regulation and function during G2 and mitotic spindle assembly checkpoints
Programtype2
Operating Grants
Orgnameinp2
Centre hospitalier de l'Université de Montréal (CHUM)
Cihramount2
$612,420
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Bcl-Xl; Cell Cycle Checkpoint; Checkpoint Kinase; Chemotherapy; Phosphatase; Phosphorylation
Abstract
The Bcl-2 family of proteins stands among the most crucial regulators of cell death (apoptosis) and performs vital function in deciding whether a cancer cell will live or die after cancer chemotherapy and radiotherapy. In addition, recent studies reveal
that members of the family also interface with cell cycle progression and DNA repair pathways, effects that are generally distinct from their functions in apoptosis. This study will focus on one member of the Bcl-2 family, and further analyse the mechanisms by
which Bcl-xL plays roles during the cell cycle checkpoints. Many efforts are already being pursued to develop new drugs targeting anti-apoptotic bcl-2 and cell cycle regulatory family members, with the ultimate goal of improving or developing alternative therapeutic protocols for cancer therapy. Thus, it is important to explore how these key regulatory molecules interface together to improve our understanding for potential clinical use of these novel cancer chemotherapy molecules.
Competitiondate
200903
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Bertrand, Richard
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $612,420~ $0~