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Grant: Operating Grant

McGill University

$1,308,735.00

Bcl-2 Family Proteins, Cell Death and the Endoplasmic Reticulum

FY 2009-10

Summary
Elimination of cells is an important process, essential for development, maintaining normal tissue status and eliminating damaged or virus-infected cells and as a front line defense for eliminating cancer cells. The elimination of cells is programmed into the cell's DNA and pathways for self-destruction of the cell are activated in response to stress signals. Mutations that interfere with the ability of a cell to kill itself or lead to killing of otherwise normal cells has serious consequences and can result in diseases such as cancer or degenerative diseases. The Bcl-2 family of proteins are amoung the key regulators of the programmed cell death pathway. Our research aims to elucidate the function of this protein family at multiple levels. Such studies have been translated into therapy with the discovery and development of obatoclax, a drug that antagonizes Bcl-2 survival proteins. This drug is currently in clinical trials to assess its promise as a new targeted anti-cancer agent.
Program
Operating Grant
Location
Quebec, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
200128
Name
Shore Gordon C
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Cell Physiology
Projecttitle
Bcl-2 Family Proteins, Cell Death and the Endoplasmic Reticulum
Programtype2
Operating Grants
Orgnameinp2
McGill University
Cihramount2
$1,308,735
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Apoptosis; Autophagy; Bap-31; Bcl-2 Family Proteins; Calcium; Chaperons; Endoplasmic Reticulum; Mitochondria; Naf-1; Programmed Cell Death
Abstract
Elimination of cells is an important process, essential for development, maintaining normal tissue status and eliminating damaged or virus-infected cells and as a front line defense for eliminating cancer cells. The elimination of cells is programmed into the cell's DNA and pathways for self-destruction of the cell are activated in response to stress signals. Mutations that interfere with the ability of a cell to kill itself or lead to killing of otherwise normal cells has serious consequences and can result in diseases such as cancer or degenerative diseases. The Bcl-2 family of proteins are amoung the key regulators of the programmed cell death pathway. Our research aims to elucidate the function of this protein family at multiple levels. Such studies have been translated into therapy with the discovery and development of obatoclax, a drug that antagonizes Bcl-2 survival proteins. This drug is currently in clinical trials to assess its promise as a new targeted anti-cancer agent.
Competitiondate
201003
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Shore, Gordon C
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $1,308,735~ $0~
McGill University - $1,308,735 Grant (2009-10) | Canada Spends