Grant: Operating Grant
University of Toronto
$364,816.00
Silencing Stat3 signaling in multiple myeloma: identifying potent small molecule inhibitors of Stat3
EF 2012-13
Résumé
Chemotherapy treatments rely heavily upon toxic drugs, which, although effective, are highly toxic and result in significant side effects, immensely reducing a cancer patient's quality of life. Frequent resistance to these toxic agents also develops, further compounding the problem. The Stat3 protein pathway confers resistance to cancer cell death in multiple myeloma(MM) tumor cells by preventing cell death and promoting cell survival. This project aims to develop novel drugs that specifically disrupt the formation of Stat3:Stat3 cancer-promoting protein complexes and prevent Stat3 gene expression programs. Through the suppression of Stat3 protein, our agents aim to kill MM tumor cells and sensitize tumors to traditional
chemotherapies, thereby reducing effective dosages and lowering toxicity. Our Stat3 inhibitors will significantly reduce the side effects associated with conventional chemotherapy as either stand-alone agents or in combinatorial adjuvant therapeutic regime.
Programme
Operating Grant
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
279257
Name
Gunning Patrick T
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Pharmaceutical Sciences
Projecttitle
Silencing Stat3 signaling in multiple myeloma: identifying potent small molecule inhibitors of Stat3
Programtype2
Operating Grants
Orgnameinp2
University of Toronto
Cihramount2
$364,816
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Anti-Cancer Drugs; Molecular Recognition; Molecular Therapeutics; Multiple Myeloma; Src Homology 2 Domains; Stat3 Protein
Abstract
Chemotherapy treatments rely heavily upon toxic drugs, which, although effective, are highly toxic and result in significant side effects, immensely reducing a cancer patient's quality of life. Frequent resistance to these toxic agents also develops, further compounding the problem. The Stat3 protein pathway confers resistance to cancer cell death in multiple myeloma(MM) tumor cells by preventing cell death and promoting cell survival. This project aims to develop novel drugs that specifically disrupt the formation of Stat3:Stat3 cancer-promoting protein complexes and prevent Stat3 gene expression programs. Through the suppression of Stat3 protein, our agents aim to kill MM tumor cells and sensitize tumors to traditional
chemotherapies, thereby reducing effective dosages and lowering toxicity. Our Stat3 inhibitors will significantly reduce the side effects associated with conventional chemotherapy as either stand-alone agents or in combinatorial adjuvant therapeutic regime.
Competitiondate
201303
Approvedterm2
4 yrs 0 mth
Pinamesdelim
Gunning, Patrick T
Approvedterm
4 ans 0 mois
Cihrcontribution2
~ $364,816~ $0~