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Grant: Project Grant

McGill University

$925,045.00

ShcA-coupled receptor tyrosine kinase signaling exposes PGC1a-dependent metabolic vulnerabilities in cancer progression and therapy

EF 2015-16

Résumé
The advent of targeted therapies, such as Tamoxifen and Herceptin, has revolutionized clinical management of a subset of breast cancer patients. Health-related knowledge generated through basic research is responsible for numerous drugs currently being evaluated in clinical trials for cancer treatment. Promising candidate drugs include those targeting the signalling machinery within cancer cells, which relays signals to promote growth, survival and metastasis, along with those targeting metabolism of tumors, which provides cells with the critical energy to fuel their uncontrolled growth. One key outstanding challenge is to develop treatments that have the best chance of success in advanced breast cancer patients. Our work has identified a novel signaling node that is commonly increased in cancer cells and which greatly impacts cancer metabolism. In this grant application, we will determine whether we can exploit these metabolic vulnerabilities of cancer cells to design metabolic therapies working alone or in combination with signalling inhibitors.
Programme
Project Grant
Bénéficiaire
Emplacement
Quebec, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
343814
Name
St-Pierre Julie
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Project Grant Competition
Projecttitle
ShcA-coupled receptor tyrosine kinase signaling exposes PGC1a-dependent metabolic vulnerabilities in cancer progression and therapy
Programtype2
Operating Grants
Orgnameinp2
McGill University
Cihramount2
$925,045
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Cancer; Metabolism; Metabolomics; Mitochondria; Pgc-1; Shca
Abstract
The advent of targeted therapies, such as Tamoxifen and Herceptin, has revolutionized clinical management of a subset of breast cancer patients. Health-related knowledge generated through basic research is responsible for numerous drugs currently being evaluated in clinical trials for cancer treatment. Promising candidate drugs include those targeting the signalling machinery within cancer cells, which relays signals to promote growth, survival and metastasis, along with those targeting metabolism of tumors, which provides cells with the critical energy to fuel their uncontrolled growth. One key outstanding challenge is to develop treatments that have the best chance of success in advanced breast cancer patients. Our work has identified a novel signaling node that is commonly increased in cancer cells and which greatly impacts cancer metabolism. In this grant application, we will determine whether we can exploit these metabolic vulnerabilities of cancer cells to design metabolic therapies working alone or in combination with signalling inhibitors.
Competitiondate
201603
Approvedterm2
5 yrs 0 mth
Pinamesdelim
St-Pierre, Julie
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $925,045~ $0~