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Grant: Project Grant

University of British Columbia

$722,926.00

Structure-based design of small molecule inhibitors of the transsulfuration pathway in Ewing Sarcoma.

EF 2024-25

Résumé
We have recently identified that human protein Cystathionine gamma lyase (CTH) plays key roles in the development of many cancers including Ewing sarcoma, breast, prostate, stomach, bladder, and colon cancers among others. We propose to use sophisticated, AI-driven, computer modelling and X-ray-based structure determination techniques to specifically design drugs which bind to these proteins and prevent their functioning. This will reduce the cancer cells' ability to survive stress, and make the cancers more susceptible to complimentary treatments like chemo- and radiation therapies. This 1-2 punch will provide an extra treatment option, especially for cancers which currently lack any effective treatments like the childhood cancer Ewing Sarcoma. It also could allow for shorter lengths when paired with current chemo- and radiation options in other cancers. Ultimately this may be more effective and have fewer side effects than current treatments.
Programme
Project Grant
Emplacement
British Columbia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
524815
Name
Cherkasov Artem
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Pharmaceutical Sciences
Projecttitle
Structure-based design of small molecule inhibitors of the transsulfuration pathway in Ewing Sarcoma.
Programtype2
Operating Grants
Orgnameinp2
University of British Columbia
Cihramount2
$722,926
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Cancer Metabolism; Cell Biology; High Throughput Screening; Hydrogen Sulfide; Reactive Oxygen Species; Structure-Based Drug Design; Sulfur Metabolism; Tumor Progression
Abstract
We have recently identified that human protein Cystathionine gamma lyase (CTH) plays key roles in the development of many cancers including Ewing sarcoma, breast, prostate, stomach, bladder, and colon cancers among others. We propose to use sophisticated, AI-driven, computer modelling and X-ray-based structure determination techniques to specifically design drugs which bind to these proteins and prevent their functioning. This will reduce the cancer cells' ability to survive stress, and make the cancers more susceptible to complimentary treatments like chemo- and radiation therapies. This 1-2 punch will provide an extra treatment option, especially for cancers which currently lack any effective treatments like the childhood cancer Ewing Sarcoma. It also could allow for shorter lengths when paired with current chemo- and radiation options in other cancers. Ultimately this may be more effective and have fewer side effects than current treatments.
Competitiondate
202503
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Cherkasov, Artem; Strynadka, Natalie C
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $722,926~ $0~