Grant: Project Grant
University of Alberta
$730,576.00
FOXM1 protein-targeted degradation and its potential role in the treatment of ovarian cancer: a medicinal chemistry approach
EF 2021-22
Résumé
The long-term goal of our research program is to understand the molecular recognition process that takes place between a special type of protein involved in cancer development and drug molecules. Specifically, we seek to establish the best way to develop novel molecules with the ability to bind to, and inhibit, the cellular activity of oncoproteins. In this regard, we propose a relatively new approach that makes use of a common mechanism used by cells to identify, tag, and decompose proteins that are no longer useful. This mechanism uses special drug molecules that are capable of "turning on" the degradation of proteins involved in the development of cancer. This technology is known in the scientific literature as protein targeting chimeras or PROTACS, and it is the subject of multiple efforts by several pharmaceutical companies, some of them here in Canada, to bring new therapeutic agents to the clinic.
This research grant will support the design and development of a series of novel molecules targeting the FOXM1 transcription factor in ovarian cancer cells, which is one of many proteins that are abnormally and consistently upregulated more than 75% of in high-grade serous carcinoma, which is the deadliest gynecologic malignancy accounting for most cases and deads in ovarian cancer.
We expect that our work will provide evidence supporting the anti-tumour activity of FOXM1 PROTACs in ovarian cancer.
Programme
Project Grant
Bénéficiaire
Emplacement
Alberta, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
463226
Name
Velazquez Carlos A
Region
Alberta
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Pharmaceutical Sciences
Projecttitle
FOXM1 protein-targeted degradation and its potential role in the treatment of ovarian cancer: a medicinal chemistry approach
Programtype2
Operating Grants
Orgnameinp2
University of Alberta
Cihramount2
$730,576
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Drug Design; Forkhead Box Proteins; Foxm1; Medicinal Chemistry; Molecular Modeling; Ovarian Cancer; Transcription; Transcription Factors
Abstract
The long-term goal of our research program is to understand the molecular recognition process that takes place between a special type of protein involved in cancer development and drug molecules. Specifically, we seek to establish the best way to develop novel molecules with the ability to bind to, and inhibit, the cellular activity of oncoproteins. In this regard, we propose a relatively new approach that makes use of a common mechanism used by cells to identify, tag, and decompose proteins that are no longer useful. This mechanism uses special drug molecules that are capable of "turning on" the degradation of proteins involved in the development of cancer. This technology is known in the scientific literature as protein targeting chimeras or PROTACS, and it is the subject of multiple efforts by several pharmaceutical companies, some of them here in Canada, to bring new therapeutic agents to the clinic.
This research grant will support the design and development of a series of novel molecules targeting the FOXM1 transcription factor in ovarian cancer cells, which is one of many proteins that are abnormally and consistently upregulated more than 75% of in high-grade serous carcinoma, which is the deadliest gynecologic malignancy accounting for most cases and deads in ovarian cancer.
We expect that our work will provide evidence supporting the anti-tumour activity of FOXM1 PROTACs in ovarian cancer.
Competitiondate
202203
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Velazquez, Carlos A
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $730,576~ $0~