Grant: Collaborative Health Research Projects
University of Manitoba
$93,271.00
Development and clinical assessment of novel biomarker drugs targeting SSAT1 for detection and therapeutic monitoring of glioblastoma
EF 2019-20
Résumé
Glioblastoma multiforme (GBM) is the most common brain tumor in adults and is a death sentence for patients. The strikingly poor survival for patients with GBM (average survival 14- 16 months following diagnosis) is due in part to limited early detection methods and an absence of effective therapeutic options. The studies proposed would establish importantevidence for the use of Health Canada approved drugs such as amantadine and rimantadine as a safe, effective and affordable way to monitor GBM. The method is based on the overproduction of a key enzyme in GBM cells called spermine/ spermadine n-acetyl transferase (SSAT1). The increased SSAT1 expression in GBM results in increased metabolism of thedrug which is detected in the blood or urine of patients with GBM. Studies will provide evidence for the effectiveness of the drug amantadine, in detecting GBM in both cell culture and accepted rodent brain tumor models. Other drugs with similar chemical structure to amantadine will be examined in the cell culture and animal models to optimize the drugbiomarker for brain penetration and tumor cell activity. The studies will conclude with an initial assessment of the selected drug biomarker in patients with GBM to determine feasibility for clinical brain tumor applications. These bench to bedside studies will be utilized by our industrial partner, BioMark Diagnostics, to help improve identification and care for patientswith GB
Programme
Collaborative Health Research Projects
Bénéficiaire
Emplacement
Manitoba, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data
Tel que publié
Application id
538823-2019
Name nom
Miller, Donald
Department département
Pharmacology and Therapeutics
Organization id
19
Institution établissement
University of Manitoba
Province en
Manitoba
Province fr
Manitoba
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2019
Competition year année de concours
2019
Award amount
93271
Program id
CHRPJ
Program name en
Collaborative Health Research Projects
Program name fr
Projets de recherche concertée sur la santé
Group en
RESEARCH PARTNERSHIPS
Group fr
PARTENARIATS DE RECHERCHE
Committee code
360
Committee name en
Collaborative Health Research Projects Selection Panel
Committee name fr
Comité de sélection de projets de recherche concertée sur la santé
Area of application code
9999
Area of application group en
Not available
Area of application group fr
Non disponible
Area of application en
Not available
Area of application fr
Non disponible
Research subject code
6400
Research subject group en
Life sciences research related to human health and disease
Research subject group fr
Sciences de la vie liées à la santé publique et aux maladies humaines
Research subject en
Life sciences research related to human health and disease
Research subject fr
Sciences de la vie liées à la santé publique et aux maladies humaines
Installment
inst:1 - 1
Partie
1
Nb partie
1
Application title
Development and clinical assessment of novel biomarker drugs targeting SSAT1 for detection and therapeutic monitoring of glioblastoma
Keyword
NSERC
Application summary
Glioblastoma multiforme (GBM) is the most common brain tumor in adults and is a death sentence for patients. The strikingly poor survival for patients with GBM (average survival 14- 16 months following diagnosis) is due in part to limited early detection methods and an absence of effective therapeutic options. The studies proposed would establish importantevidence for the use of Health Canada approved drugs such as amantadine and rimantadine as a safe, effective and affordable way to monitor GBM. The method is based on the overproduction of a key enzyme in GBM cells called spermine/ spermadine n-acetyl transferase (SSAT1). The increased SSAT1 expression in GBM results in increased metabolism of thedrug which is detected in the blood or urine of patients with GBM. Studies will provide evidence for the effectiveness of the drug amantadine, in detecting GBM in both cell culture and accepted rodent brain tumor models. Other drugs with similar chemical structure to amantadine will be examined in the cell culture and animal models to optimize the drugbiomarker for brain penetration and tumor cell activity. The studies will conclude with an initial assessment of the selected drug biomarker in patients with GBM to determine feasibility for clinical brain tumor applications. These bench to bedside studies will be utilized by our industrial partner, BioMark Diagnostics, to help improve identification and care for patientswith GB