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Grant: Operating Grant - Priority Announcement: Breast Cancer

University of Manitoba

$100,000.00

Beyond the Estrogen Receptor: involvement of kinases in estrogen signaling in normal and malignant human breast epithelial cells

EF 2014-15

Résumé
Targeting estrogen receptor (ER) with tamoxifen, is successful in treating and preventing breast cancer. Nevertheless, such therapies are limited due to resistance. Newer therapies, targeting ER, are also likely limited by development of resistance. Understanding the mechanisms of ER action holds promise for further increasing the approaches to treat ER+ breast cancer, the most frequent type of breast cancer. The more targets, the more likely the disease can be controlled. The development of more precise biomarkers of therapy response is valuable, so that the most appropriate therapies can be used quickly with minimal side-effects. We discovered that certain combinations of chemical changes called phosphorylation, on the surface of ER are more accurate biomarkers of prognosis than those currently used. We don't think these changes occur in normal breast cells. Therefore the enzymes that cause these changes are ideal targets for developing new endocrine therapies for treating and preventing breast cancer.
Programme
Operating Grant - Priority Announcement: Breast Cancer
Emplacement
Manitoba, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
328763
Name
Murphy Leigh C
Region
Manitoba
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Endocrinology
Projecttitle
Beyond the Estrogen Receptor: involvement of kinases in estrogen signaling in normal and malignant human breast epithelial cells
Programtype2
Operating Grants
Orgnameinp2
University of Manitoba
Cihramount2
$100,000
Cihrequipment2
$0
Programname2
Operating Grant - Priority Announcement: Breast Cancer
Keyworddelim
Biochemistry; Biomarker; Breast Cancer; Cell Biology; Estrogen Receptor; Immunohistochemistry; Kinase; Molecular Endocrinology; Molecular Pathology; Normal Breast
Abstract
Targeting estrogen receptor (ER) with tamoxifen, is successful in treating and preventing breast cancer. Nevertheless, such therapies are limited due to resistance. Newer therapies, targeting ER, are also likely limited by development of resistance. Understanding the mechanisms of ER action holds promise for further increasing the approaches to treat ER+ breast cancer, the most frequent type of breast cancer. The more targets, the more likely the disease can be controlled. The development of more precise biomarkers of therapy response is valuable, so that the most appropriate therapies can be used quickly with minimal side-effects. We discovered that certain combinations of chemical changes called phosphorylation, on the surface of ER are more accurate biomarkers of prognosis than those currently used. We don't think these changes occur in normal breast cells. Therefore the enzymes that cause these changes are ideal targets for developing new endocrine therapies for treating and preventing breast cancer.
Competitiondate
201503
Approvedterm2
1 yr 0 mth
Pinamesdelim
Murphy, Leigh C
Approvedterm
1 an 0 mois
Cihrcontribution2
~ $100,000~ $0~