Grant: Doctoral: Vanier Canada Graduate Scholarships
University of Ottawa
$150,000.00
The role of PTGS2 signaling in ovulation-associated Brca1 repression
FY 2014-15
Summary
Ovarian cancer is one of the deadliest cancers women face, with less than 40% surviving the disease. We need new methods to prevent ovarian cancer, and new screening methods to detect it in its early treatable stages. Very little is known about how ovarian cancer occurs, but there are hints that have led us on our current research path. These hints have come from our research on the two biggest ovarian cancer risk factors: ovulation and the Brca1 gene. We know that the risk of ovarian cancer increases proportionally with the number of ovulations. Every time a woman ovulates, the egg causes a small amount of damage to the ovary that the body then repairs. The repair process is dangerous since it is a time when cells are more at risk to becoming cancerous. The other well established risk factor is an inactive Brca1 gene. The Brca1 gene is involved in the cell's safety measures that help prevent cancer. Interestingly, the Brca1 gene is inactive in the majority of ovarian cancers hinting that this gene plays a large role in causing this disease. The safety measures put in place by the Brca1 gene are particularly important during the repair process that occurs in the ovary after ovulation. Our research investigates the link between ovulation and the Brca1 gene, which has never been studied before. We have evidence for the first time that the two biggest risk factors, increased ovulation and inactive Brca1 might be related. We think that ovulation might cause inactivation of Brca1 thereby removing the cells safeguard against cancer. This project aims to study the molecular basis of how ovulation inactivates Brca1 and why this leads to ovarian cancer. This project has great potential to finally understand why ovulation and inactive Brca1 are risk factors. We are very optimistic that this research will improve our understanding of ovarian cancer and lead to new therapeutic interventions to prevent ovarian cancer and detect it while it is still treatable.
Department
Program
Doctoral: Vanier Canada Graduate Scholarships
Recipient
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
318138
Name
McCloskey Curtis
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Vanier Canada Graduate Scholarships CIHR
Projecttitle
The role of PTGS2 signaling in ovulation-associated Brca1 repression
Programtype2
Studentship Programs
Orgnameinp2
University of Ottawa
Cihramount2
$150,000
Cihrequipment2
$0
Programname2
Doctoral: Vanier Canada Graduate Scholarships
Keyworddelim
Brca1; Cancer Initiation; Chromatin; Epigenetics; Epithelial Ovarian Cancer; Hypermethylation; Ovarian Cancer; Ovulation; Ptgs2; Women'S Health
Abstract
Ovarian cancer is one of the deadliest cancers women face, with less than 40% surviving the disease. We need new methods to prevent ovarian cancer, and new screening methods to detect it in its early treatable stages. Very little is known about how ovarian cancer occurs, but there are hints that have led us on our current research path. These hints have come from our research on the two biggest ovarian cancer risk factors: ovulation and the Brca1 gene. We know that the risk of ovarian cancer increases proportionally with the number of ovulations. Every time a woman ovulates, the egg causes a small amount of damage to the ovary that the body then repairs. The repair process is dangerous since it is a time when cells are more at risk to becoming cancerous. The other well established risk factor is an inactive Brca1 gene. The Brca1 gene is involved in the cell's safety measures that help prevent cancer. Interestingly, the Brca1 gene is inactive in the majority of ovarian cancers hinting that this gene plays a large role in causing this disease. The safety measures put in place by the Brca1 gene are particularly important during the repair process that occurs in the ovary after ovulation. Our research investigates the link between ovulation and the Brca1 gene, which has never been studied before. We have evidence for the first time that the two biggest risk factors, increased ovulation and inactive Brca1 might be related. We think that ovulation might cause inactivation of Brca1 thereby removing the cells safeguard against cancer. This project aims to study the molecular basis of how ovulation inactivates Brca1 and why this leads to ovarian cancer. This project has great potential to finally understand why ovulation and inactive Brca1 are risk factors. We are very optimistic that this research will improve our understanding of ovarian cancer and lead to new therapeutic interventions to prevent ovarian cancer and detect it while it is still treatable.
Competitiondate
201411
Approvedterm2
3 yrs 0 mth
Pinamesdelim
McCloskey, Curtis
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $150,000~ $0~