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Grant: Operating Grant - Priority Announcement: Breast Cancer

McMaster University

$374,398.00

Investigation of Shank-interacting protein-like 1 (SIPL1)-mediated PTEN inactivation during breast tumorigenesis

EF 2009-10

Résumé
PTEN is a critical tumour suppressor that prevents breast cancer formation. Clinical observations have shown that a loss of PTEN occurs in high percentages (up to 50%) of HER2-positive and basal-like breast cancers, the two subgroups that are associated with a poor outcome. However, our knowledge on how PTEN is inactivated in breast cancer is incomplete. We propose here that although a large proportion of breast cancers contain PTEN, the protein may not function properly. Consistent with our hypothesis, we identified a protein (called SIPL1) that reduces PTEN function. Furthermore, we demonstrated that SIPL1 inactivates PTEN in breast cancer cells and importantly, associates with a loss of PTEN function in primary breast cancers obtained directly from patients. This strongly suggests that SIPL1 inactivates PTEN during breast cancer formation. In this study, we will closely examine the relationship between SIPL1 and the loss of PTEN function in breast cancer as well as how SIPL1 reduces PTEN function during breast cancer formation. As the loss of PTEN function is a major cause of therapeutic failure for breast cancer, this research may lead to the development of novel diagnostic and therapeutic approaches for patients with breast cancer.
Programme
Operating Grant - Priority Announcement: Breast Cancer
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
207777
Name
Tang Damu
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Molecular & Cellular Biology of Cancer
Projecttitle
Investigation of Shank-interacting protein-like 1 (SIPL1)-mediated PTEN inactivation during breast tumorigenesis
Programtype2
Operating Grants
Orgnameinp2
McMaster University
Cihramount2
$374,398
Cihrequipment2
$0
Programname2
Operating Grant - Priority Announcement: Breast Cancer
Keyworddelim
Breast Cancer; Pi3-Akt Signaling; Pten; Pten Negative Regulator
Abstract
PTEN is a critical tumour suppressor that prevents breast cancer formation. Clinical observations have shown that a loss of PTEN occurs in high percentages (up to 50%) of HER2-positive and basal-like breast cancers, the two subgroups that are associated with a poor outcome. However, our knowledge on how PTEN is inactivated in breast cancer is incomplete. We propose here that although a large proportion of breast cancers contain PTEN, the protein may not function properly. Consistent with our hypothesis, we identified a protein (called SIPL1) that reduces PTEN function. Furthermore, we demonstrated that SIPL1 inactivates PTEN in breast cancer cells and importantly, associates with a loss of PTEN function in primary breast cancers obtained directly from patients. This strongly suggests that SIPL1 inactivates PTEN during breast cancer formation. In this study, we will closely examine the relationship between SIPL1 and the loss of PTEN function in breast cancer as well as how SIPL1 reduces PTEN function during breast cancer formation. As the loss of PTEN function is a major cause of therapeutic failure for breast cancer, this research may lead to the development of novel diagnostic and therapeutic approaches for patients with breast cancer.
Competitiondate
201003
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Tang, Damu
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $374,398~ $0~