Grant: Travel Awards - Institute Community Support
University of Saskatchewan
$1,000.00
Quantitative phosphoproteomics analyses identifies candidate substrates of the tumor suppressor tyrosine kinase, FRK in glioblastoma cells
EF 2017-18
Résumé
FRK (Fyn-related kinase) is a non-receptor tyrosine kinase that belongs to the BRK (Breast tumor kinase) family. Previous studies as well as current studies in our lab have shown that FRK pays a candidate tumor suppressor role in glioblastomas. Our studies have further shown that FRK suppresses cell growth and migration in a kinase-dependent manner. In the present study, we used quantitative phosphoproteomics analysis and identified the candidate substrates of FRK in glioblastoma cells. Our study is the first to identify the vast array of novel FRK candidate substrates which further reveals novel mechanisms by which FRK promotes tumor suppressor functions in glioblastoma cells.
Programme
Travel Awards - Institute Community Support
Bénéficiaire
Emplacement
Saskatchewan, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
368470
Name
Goel Raghuveera K
Region
Saskatchewan
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Institute of Cancer Research
Projecttitle
Quantitative phosphoproteomics analyses identifies candidate substrates of the tumor suppressor tyrosine kinase, FRK in glioblastoma cells
Programtype2
Undefined
Orgnameinp2
University of Saskatchewan
Cihramount2
$1,000
Cihrequipment2
$0
Programname2
Travel Awards - Institute Community Support
Keyworddelim
Ics Travel Awards
Abstract
FRK (Fyn-related kinase) is a non-receptor tyrosine kinase that belongs to the BRK (Breast tumor kinase) family. Previous studies as well as current studies in our lab have shown that FRK pays a candidate tumor suppressor role in glioblastomas. Our studies have further shown that FRK suppresses cell growth and migration in a kinase-dependent manner. In the present study, we used quantitative phosphoproteomics analysis and identified the candidate substrates of FRK in glioblastoma cells. Our study is the first to identify the vast array of novel FRK candidate substrates which further reveals novel mechanisms by which FRK promotes tumor suppressor functions in glioblastoma cells.
Competitiondate
201707
Approvedterm2
1 yr 0 mth
Pinamesdelim
Goel, Raghuveera K
Approvedterm
1 an 0 mois
Cihrcontribution2
Inst of Cancer Research~ $1,000~ $0~