Grant: Operating Grant
Research Institute of the McGill University Health Centre
$710,040.00
Coagulation system effectors as regulators of tumour dormancy and therapeutic targets
EF 2013-14
Résumé
Cancers can be controlled even if the mutated cells remain viable, but are locked in a state known as dormancy. One feature of progressive cancers is the activation of the blood clotting (coagulation) system. We study brain tumours where we observed that cells unable to form tumours also lack the clotting protein - tissue factor (TF). These tumour cells remain viable, but stay dormant in the brain of mice, often for months. If TF is triggered tumour growth ensues. We also observed that this 'awakening' is linked to the ability of the clotting system (especially TF) to activate inflammation and blood vessel growth around cancer cells, and these processes cause cancer cell DNA to mutate. This effect has not been recognized, and we will study it deeper, to find ways to prevent blood clotting reaction from mutating cancer cells and triggering them to grow and invade tissues.
Programme
Operating Grant
Emplacement
Quebec, Canada
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
292199
Name
Rak Janusz
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Cancer Progression & Therapeutics 2
Projecttitle
Coagulation system effectors as regulators of tumour dormancy and therapeutic targets
Programtype2
Operating Grants
Orgnameinp2
Research Institute of the McGill University Health Centre
Cihramount2
$710,040
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Angiogenesis; Antiangiogenesis; Anticoagulants; Biomarker; Coagulation Factors; Dormancy; Glioma; Inflammation; Oncogenes; Targeted Agents
Abstract
Cancers can be controlled even if the mutated cells remain viable, but are locked in a state known as dormancy. One feature of progressive cancers is the activation of the blood clotting (coagulation) system. We study brain tumours where we observed that cells unable to form tumours also lack the clotting protein - tissue factor (TF). These tumour cells remain viable, but stay dormant in the brain of mice, often for months. If TF is triggered tumour growth ensues. We also observed that this 'awakening' is linked to the ability of the clotting system (especially TF) to activate inflammation and blood vessel growth around cancer cells, and these processes cause cancer cell DNA to mutate. This effect has not been recognized, and we will study it deeper, to find ways to prevent blood clotting reaction from mutating cancer cells and triggering them to grow and invade tissues.
Competitiondate
201309
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Rak, Janusz
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $710,040~ $0~