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Grant: CIHR Fellowship

Direct Payment

$150,000.00

Understanding p53-status in modulating the crosstalk between the immune microenvironment and pancreatic cancer

FY 2015-16

Summary
Everyday, about 540 Canadians will be newly diagnosed with cancer. Despite this staggering statistic, majority of individuals will not go on to develop cancer. The following protection is largely contributed by our immune surveillance system. In addition to fighting off bacteria and viruses, our immune system has also evolved to monitor and eliminate cancerous cells. Importantly however, cancerous cells have developed mechanisms to counteract, evade and suppress our immune response. Although the genetic mutations underlying pancreatic cancer are well characterized, it remains a devastating disease. Treatments to date have failed and pancreatic cancer has the lowest five-year survival rate among patients. Better understanding of the dynamic interplay between cancerous cells and immunity will allow us to develop novel targets for pancreatic cancer treatments. Indeed, successful breakthroughs in the treatment of another cancer, melanoma, have come from targeting tumour-induced immune suppression. Therefore, our studies of cancer immune-suppression in the context of genetics will allow us to further harness the natural anti-tumour action of our immune system to combat pancreatic cancer.
Program
CIHR Fellowship
Location
United Kingdom
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
339035
Name
Blagih Julianna
Country
United Kingdom
Orgtype
Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Fellowships - Post-PhD
Projecttitle
Understanding p53-status in modulating the crosstalk between the immune microenvironment and pancreatic cancer
Programtype2
Fellowship Programs
Orgnameinp2
Direct Payment
Cihramount2
$150,000
Cihrequipment2
$0
Programname2
CIHR Fellowship
Keyworddelim
Cancer Immunology; Kras; P53; Pancreatic Cancer
Abstract
Everyday, about 540 Canadians will be newly diagnosed with cancer. Despite this staggering statistic, majority of individuals will not go on to develop cancer. The following protection is largely contributed by our immune surveillance system. In addition to fighting off bacteria and viruses, our immune system has also evolved to monitor and eliminate cancerous cells. Importantly however, cancerous cells have developed mechanisms to counteract, evade and suppress our immune response. Although the genetic mutations underlying pancreatic cancer are well characterized, it remains a devastating disease. Treatments to date have failed and pancreatic cancer has the lowest five-year survival rate among patients. Better understanding of the dynamic interplay between cancerous cells and immunity will allow us to develop novel targets for pancreatic cancer treatments. Indeed, successful breakthroughs in the treatment of another cancer, melanoma, have come from targeting tumour-induced immune suppression. Therefore, our studies of cancer immune-suppression in the context of genetics will allow us to further harness the natural anti-tumour action of our immune system to combat pancreatic cancer.
Competitiondate
201511
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Blagih, Julianna
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $150,000~ $0~