Canada Spends Logo

Explorez notre analyse du budget 2026

Grant: Project Grant

Children's Hospital of Eastern Ontario Research Institute Inc

$910,350.00

Identifying novel strategies for leukemia prevention using zebrafish models of dnajc21-mutant Shwachman Diamond syndrome

EF 2022-23

Résumé
Shwachman Diamond syndrome (SDS) is a type of bone marrow failure that frequently presents in children and young adults. It results in poor growth, reduced production of white blood cells and pancreatic dysfunction. SDS is caused by abnormalities in genes, including one called DNAJC21, which play important roles in assembling ribosomes that are required in all cells to make proteins. SDS patients are at a much higher risk of developing high-risk types of leukemia. Current definitive treatment for SDS requires a bone marrow transplant and is associated with many potential complications and risks. There is an unmet need for developing treatments that are specific to SDS biology that could help restore normal blood cell numbers with the goal of preventing the development of leukemia. The zebrafish has very similar but more rapid blood development than humans, making it an ideal animal model for studying SDS and how it evolves into leukemia. Our laboratory has extensive experience in this area, and we have already developed zebrafish carrying mutations in the zebrafish DNAJC21 gene. These mutant fish have stunted growth and reduced white blood cell production similar to SDS patients. To model leukemia progression, we have introduced additional mutations in genes frequently seen in SDS patients with leukemia. We believe that the metabolism level of these blood cells is low when the bone marrow isn't working well and becomes high when it develops into leukemia. We will investigate if these metabolic factors can be targeted to stop leukemia progression. Lastly, we will use cells from SDS patients to check for the genetic changes that we find in our zebrafish and look for drugs that can rescue blood defects and potentially halt the development of leukemia. This study will improve our understanding of SDS and other conditions that increase the risk of developing leukemia and identify drugs for leukemia prevention.
Programme
Project Grant
Emplacement
Ontario, Canada
Type de bénéficiaire
Other
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
468557
Name
Berman Jason N
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Cancer Progression & Therapeutics
Projecttitle
Identifying novel strategies for leukemia prevention using zebrafish models of dnajc21-mutant Shwachman Diamond syndrome
Programtype2
Operating Grants
Orgnameinp2
Children's Hospital of Eastern Ontario Research Institute Inc
Cihramount2
$910,350
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Bone Marrow Failure; Leukemia; Metabolomics; Therapeutics; Zebrafish
Abstract
Shwachman Diamond syndrome (SDS) is a type of bone marrow failure that frequently presents in children and young adults. It results in poor growth, reduced production of white blood cells and pancreatic dysfunction. SDS is caused by abnormalities in genes, including one called DNAJC21, which play important roles in assembling ribosomes that are required in all cells to make proteins. SDS patients are at a much higher risk of developing high-risk types of leukemia. Current definitive treatment for SDS requires a bone marrow transplant and is associated with many potential complications and risks. There is an unmet need for developing treatments that are specific to SDS biology that could help restore normal blood cell numbers with the goal of preventing the development of leukemia. The zebrafish has very similar but more rapid blood development than humans, making it an ideal animal model for studying SDS and how it evolves into leukemia. Our laboratory has extensive experience in this area, and we have already developed zebrafish carrying mutations in the zebrafish DNAJC21 gene. These mutant fish have stunted growth and reduced white blood cell production similar to SDS patients. To model leukemia progression, we have introduced additional mutations in genes frequently seen in SDS patients with leukemia. We believe that the metabolism level of these blood cells is low when the bone marrow isn't working well and becomes high when it develops into leukemia. We will investigate if these metabolic factors can be targeted to stop leukemia progression. Lastly, we will use cells from SDS patients to check for the genetic changes that we find in our zebrafish and look for drugs that can rescue blood defects and potentially halt the development of leukemia. This study will improve our understanding of SDS and other conditions that increase the risk of developing leukemia and identify drugs for leukemia prevention.
Competitiondate
202209
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Berman, Jason N
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $910,350~ $0~