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Grant: Operating Grant

University of British Columbia

$686,778.00

Targeting the YB-1 pathway to overcome breast cancer recurrence

EF 2010-11

Résumé
Worldwide there are 1 million new cases of breast cancer and the greatest challenge is tumours that are resistant to conventional therapies. This is not all that uncommon given that 30% of women will experience breast cancer recurrence following their initial treatment. Further complicating matters, once the cancer returns womens are 100 times more likely to die from the disease. We discovered a protein referred to as YB-1 and its activated form P-YB-1S102 are expressed in ~50% of all breast cancers based on measuring it in ~5500 cases. It holds promise as a therapeutic target for this disease because it mediates resistance and further breast cancer cells continue to depend on it even when they have developed drug insensitivity. In this proposal we will explore the possibility that we can inhibit YB-1 using drugs that block its activation. In order to translate this quickly we will screen drugs that are currently in clinical trials in the hope that there may be agents "in the pipline" that could be used to tailor treatment.
Programme
Operating Grant
Emplacement
British Columbia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
223826
Name
Dunn Sandra E
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Cancer Progression & Therapeutics
Projecttitle
Targeting the YB-1 pathway to overcome breast cancer recurrence
Programtype2
Operating Grants
Orgnameinp2
University of British Columbia
Cihramount2
$686,778
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Breast Cancer; Cd24; Cd44; Chip-Sequencing; Experimental Therapeutics; Kinase Inhibitors; Rsk; Tumour Tissue Microarrays; Tumour-Initiating Cells; Yb-1
Abstract
Worldwide there are 1 million new cases of breast cancer and the greatest challenge is tumours that are resistant to conventional therapies. This is not all that uncommon given that 30% of women will experience breast cancer recurrence following their initial treatment. Further complicating matters, once the cancer returns womens are 100 times more likely to die from the disease. We discovered a protein referred to as YB-1 and its activated form P-YB-1S102 are expressed in ~50% of all breast cancers based on measuring it in ~5500 cases. It holds promise as a therapeutic target for this disease because it mediates resistance and further breast cancer cells continue to depend on it even when they have developed drug insensitivity. In this proposal we will explore the possibility that we can inhibit YB-1 using drugs that block its activation. In order to translate this quickly we will screen drugs that are currently in clinical trials in the hope that there may be agents "in the pipline" that could be used to tailor treatment.
Competitiondate
201103
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Dunn, Sandra E
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $686,778~ $0~