Canada Spends Logo

Explorez notre analyse du budget 2026

Grant: Doctoral: Vanier Canada Graduate Scholarships

University of British Columbia

$150,000.00

Characterizing the Role of Capicua (CIC) Mutations in Oligodendroglioma

EF 2015-16

Résumé
Canadian Cancer Statistics estimates that >2,000 Canadians will be diagnosed with gliomas, a type of brain tumour, in 2015 alone. Despite their relatively common occurrence, current therapies against gliomas are often only marginally effective, and new, more effective treatments are desperately needed. For instance, glioblastomas, the most common and severe type of glioma, are generally associated with a survival of only ~15 months. Oligodendrogliomas (ODGs) are lower-grade gliomas that are of particular interest because they generally present a better prognosis than their high-grade counterparts. Cancer is a genetic disease that arises when mutations occur in specific genes. Genes can be defined as discrete units of DNA that contain instructions on how to construct individual proteins; proteins, in turn, are complex molecules that carry out specific functions within the cell. The amount of protein produced is largely dependent on the expression level of the gene, which can itself be modulated by several processes. Though each tumour is unique, many types and subtypes of cancers are characterized by recurrent mutations that contribute to the behaviour of those particular tumours. This holds true for ODGs, which are associated with several genetic abnormalities, including frequent mutations in a gene named Capicua (CIC). The CIC protein is able to regulate the expression of other genes, and preliminary analyses from our group have identified >350 genes whose expression is potentially regulated by CIC. Though CIC is mutated in ~70% of ODGs, little is known about its function in cancer cells. By studying CIC's interaction network and the effect of recurrent mutations on CIC's function, we will be able to uncover the role of CIC mutations in ODG progression. This may in turn lead to the identification of novel therapeutic targets, providing more effective treatment options for ODGs and for other types of gliomas that are currently associated with a short survival time.
Programme
Doctoral: Vanier Canada Graduate Scholarships
Emplacement
British Columbia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
339628
Name
LeBlanc Veronique G
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Vanier Canada Graduate Scholarships CIHR
Projecttitle
Characterizing the Role of Capicua (CIC) Mutations in Oligodendroglioma
Programtype2
Studentship Programs
Orgnameinp2
University of British Columbia
Cihramount2
$150,000
Cihrequipment2
$0
Programname2
Doctoral: Vanier Canada Graduate Scholarships
Keyworddelim
Bioinformatics; Cancer Biology; Cancer Epigenomics; Cancer Genomics; Glioma; Transcription Factor
Abstract
Canadian Cancer Statistics estimates that >2,000 Canadians will be diagnosed with gliomas, a type of brain tumour, in 2015 alone. Despite their relatively common occurrence, current therapies against gliomas are often only marginally effective, and new, more effective treatments are desperately needed. For instance, glioblastomas, the most common and severe type of glioma, are generally associated with a survival of only ~15 months. Oligodendrogliomas (ODGs) are lower-grade gliomas that are of particular interest because they generally present a better prognosis than their high-grade counterparts. Cancer is a genetic disease that arises when mutations occur in specific genes. Genes can be defined as discrete units of DNA that contain instructions on how to construct individual proteins; proteins, in turn, are complex molecules that carry out specific functions within the cell. The amount of protein produced is largely dependent on the expression level of the gene, which can itself be modulated by several processes. Though each tumour is unique, many types and subtypes of cancers are characterized by recurrent mutations that contribute to the behaviour of those particular tumours. This holds true for ODGs, which are associated with several genetic abnormalities, including frequent mutations in a gene named Capicua (CIC). The CIC protein is able to regulate the expression of other genes, and preliminary analyses from our group have identified >350 genes whose expression is potentially regulated by CIC. Though CIC is mutated in ~70% of ODGs, little is known about its function in cancer cells. By studying CIC's interaction network and the effect of recurrent mutations on CIC's function, we will be able to uncover the role of CIC mutations in ODG progression. This may in turn lead to the identification of novel therapeutic targets, providing more effective treatment options for ODGs and for other types of gliomas that are currently associated with a short survival time.
Competitiondate
201511
Approvedterm2
3 yrs 0 mth
Pinamesdelim
LeBlanc, Veronique G
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $150,000~ $0~