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Grant: Doctoral: Vanier Canada Graduate Scholarships

Queen's University (Kingston, Ontario)

$150,000.00

Characterizing Clonal Hematopoiesis-Induced Changes in the Tumour Microenvironment to Improve Immunotherapy Efficacy

FY 2024-25

Summary
All the blood cells in our body are produced by cells in our bone marrow called hematopoietic stem cells (HSCs). As we get older, the DNA in our HSCs can become mutated, causing these cells to produce more blood cells than normal - we call this condition clonal hematopoiesis (CH). It is estimated that 10-20% of people over 70 have CH. People with CH are at a higher risk of chronic diseases like heart disease and cancer. This is because our immune (white blood) cells are also affected by the mutations that cause CH, leading them to produce more disease-causing inflammation. Researchers are still unsure what effects CH has on cancers. Some studies have shown that CH is linked with an increased risk of a patient's cancer progressing, while other have shown that the mutations that cause CH can help your immune system fight cancer and that CH can help protect people from cancer. Our research is trying to better understand CH in cancer so that we can use this knowledge to improve cancer immunotherapies, which are a new generation of cancer treatments that use the power of the immune system to fight cancer. Immunotherapies can be very effective in treating cancer, but they still have a low success rate because it is difficult to predict who will respond to the treatments. We have started a study looking at 10,000 tumours, comparing tumours from people with and without CH to see what is different about their immune response. Some early results from this study show that by creating inflammation, CH can make a type of brain cancer called glioblastoma even worse, but at the same time may make people with glioblastoma better candidates for immunotherapy. By studying glioblastoma biopsy samples from clinical trials and creating experimental models of CH and glioblastoma, we hope that we can better understand this effect and help discover new and effective immunotherapy treatments for cancer.
Program
Doctoral: Vanier Canada Graduate Scholarships
Location
Ontario, Canada
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
517223
Name
Buttigieg Marco M
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Vanier Canada Graduate Scholarships CIHR
Projecttitle
Characterizing Clonal Hematopoiesis-Induced Changes in the Tumour Microenvironment to Improve Immunotherapy Efficacy
Programtype2
Studentship Programs
Orgnameinp2
Queen's University (Kingston, Ontario)
Cihramount2
$150,000
Cihrequipment2
$0
Programname2
Doctoral: Vanier Canada Graduate Scholarships
Keyworddelim
Aging; Cancer Immunology; Genomics; Hematopoiesis; Inflammation
Abstract
All the blood cells in our body are produced by cells in our bone marrow called hematopoietic stem cells (HSCs). As we get older, the DNA in our HSCs can become mutated, causing these cells to produce more blood cells than normal - we call this condition clonal hematopoiesis (CH). It is estimated that 10-20% of people over 70 have CH. People with CH are at a higher risk of chronic diseases like heart disease and cancer. This is because our immune (white blood) cells are also affected by the mutations that cause CH, leading them to produce more disease-causing inflammation. Researchers are still unsure what effects CH has on cancers. Some studies have shown that CH is linked with an increased risk of a patient's cancer progressing, while other have shown that the mutations that cause CH can help your immune system fight cancer and that CH can help protect people from cancer. Our research is trying to better understand CH in cancer so that we can use this knowledge to improve cancer immunotherapies, which are a new generation of cancer treatments that use the power of the immune system to fight cancer. Immunotherapies can be very effective in treating cancer, but they still have a low success rate because it is difficult to predict who will respond to the treatments. We have started a study looking at 10,000 tumours, comparing tumours from people with and without CH to see what is different about their immune response. Some early results from this study show that by creating inflammation, CH can make a type of brain cancer called glioblastoma even worse, but at the same time may make people with glioblastoma better candidates for immunotherapy. By studying glioblastoma biopsy samples from clinical trials and creating experimental models of CH and glioblastoma, we hope that we can better understand this effect and help discover new and effective immunotherapy treatments for cancer.
Competitiondate
202410
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Buttigieg, Marco M
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $150,000~ $0~
Queen's University (Kingston, Ontario) - $150,000 Gra… | Canada Spends