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Grant: Project Grant

University of British Columbia

$413,100.00

Identification of HOXB13 inhibitors to treat castrate-resistant prostate cancer

EF 2019-20

Résumé
Prostate cancer (PCa) affects an estimated one out of every seven Canadian men in their lifetime. The standard of care to treat recurrent or metastatic disease is designed to inhibit androgen receptor activation. While treatment is initially successful, almost all patients eventually develop resistance and progress to an aggressive "castrate-resistant" state. Even with the introduction of more potent therapeutics the median survival for these patients is less than 3 years. There is therefore a critical need for drugs that target novel molecular drivers of prostate cancer. HOXB13 is a prostate-specific protein that is essential to the growth of almost all prostate cancers experimental models. Importantly, it does not affect any other tissue. Given this critical role, HOXB13 represents a promising target to treat prostate cancer. The proposed project will first characterize the role of HOXB13 in PCa. Using these results we will identify small molecule inhibitors that directly inhibit HOXB13. From this study, a new class of inhibitors will be created which could lead to the development of novel therapeutic strategies to treat lethal prostate cancer
Programme
Project Grant
Emplacement
British Columbia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
419965
Name
Gleave Martin E
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Cancer Biology & Therapeutics 2
Projecttitle
Identification of HOXB13 inhibitors to treat castrate-resistant prostate cancer
Programtype2
Operating Grants
Orgnameinp2
University of British Columbia
Cihramount2
$413,100
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Hoxb13; Prostate Cancer; Small Molecule Inhibitors; Transcriptional Regulation
Abstract
Prostate cancer (PCa) affects an estimated one out of every seven Canadian men in their lifetime. The standard of care to treat recurrent or metastatic disease is designed to inhibit androgen receptor activation. While treatment is initially successful, almost all patients eventually develop resistance and progress to an aggressive "castrate-resistant" state. Even with the introduction of more potent therapeutics the median survival for these patients is less than 3 years. There is therefore a critical need for drugs that target novel molecular drivers of prostate cancer. HOXB13 is a prostate-specific protein that is essential to the growth of almost all prostate cancers experimental models. Importantly, it does not affect any other tissue. Given this critical role, HOXB13 represents a promising target to treat prostate cancer. The proposed project will first characterize the role of HOXB13 in PCa. Using these results we will identify small molecule inhibitors that directly inhibit HOXB13. From this study, a new class of inhibitors will be created which could lead to the development of novel therapeutic strategies to treat lethal prostate cancer
Competitiondate
202003
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Gleave, Martin E; Lack, Nathan A
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $413,100~ $0~