Grant: Operating Grant
Ottawa Hospital Research Institute
$731,350.00
Systems biology approach to elucidating the role of TAL1/SCL in T-cell acute lymphoblastic leukemia
EF 2009-10
Résumé
T cell acute lymphoblastic leukemia (T-ALL) is an aggressive cancer occurring in children and adults wherein cells belonging to the immune system acquire a defect in their normal regulatory circuitry and grow in an uncontrolled manner. In many instances, T-ALL is caused when the TAL1 protein (which is normally present in red blood cells) is aberrantly produced in white blood cells. This disrupts the growth control mechanism of specific cells of the immune system. To understand how this mis-expression of TAL1 in white blood cells leads to leukemia, we have recently identified the genes that are deregulated in diseased cells. In this new application, we will further these studies to examine how TAL1 interacts with specific proteins present in white blood cells, leading to deregulation of these genes. Our novel approach could lead to new therapy for treating children and adults affected with this deadly disease.
Programme
Operating Grant
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Other
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
189369
Name
Brand Marjorie C
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Molecular & Cellular Biology of Cancer
Projecttitle
Systems biology approach to elucidating the role of TAL1/SCL in T-cell acute lymphoblastic leukemia
Programtype2
Operating Grants
Orgnameinp2
Ottawa Hospital Research Institute
Cihramount2
$731,350
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Chromatin Immunoprecipitation Deep Sequencing (Chip-Seq); Gene Expression; Icat Quantitative Proteomics; Knockdown By Rna Interference; Scl; T-Cell Acute Lymphoblastic Leukemia; Tal1; Transcription
Abstract
T cell acute lymphoblastic leukemia (T-ALL) is an aggressive cancer occurring in children and adults wherein cells belonging to the immune system acquire a defect in their normal regulatory circuitry and grow in an uncontrolled manner. In many instances, T-ALL is caused when the TAL1 protein (which is normally present in red blood cells) is aberrantly produced in white blood cells. This disrupts the growth control mechanism of specific cells of the immune system. To understand how this mis-expression of TAL1 in white blood cells leads to leukemia, we have recently identified the genes that are deregulated in diseased cells. In this new application, we will further these studies to examine how TAL1 interacts with specific proteins present in white blood cells, leading to deregulation of these genes. Our novel approach could lead to new therapy for treating children and adults affected with this deadly disease.
Competitiondate
200909
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Brand, Marjorie C
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $731,350~ $0~