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Grant: Project Grant

University of British Columbia

$887,400.00

A systems glycobiology platform for revealing new immunotherapy targets in acute myeloid leukemia

FY 2023-24

Summary
All of the cells in our body are coated with different types of sugar molecules. Cells in our immune system have ways of "tasting" these sugars. Some types of sugars taste good to our immune system, signaling that our cells are healthy and that everything is normal. Other sugars (like those attached to invading bacteria, viruses or cancer cells) taste bad to our immune cells, triggering them to activate and try to protect us from disease. Sometimes our cells can become altered in ways that lead them to produce different or abnormal types of sugar molecules on their surface. When this happens, it can lead our immune cells to overlook unhealthy cells (in the case of cancer). Understanding the details of how this happens can help us develop new drugs to treat such diseases. We face the problem, however, that these cellular sugar molecules are not like the sugar that we eat. Cellular sugars are notoriously chemically complex, making it difficult to predict exactly how specific types of sugar molecules will affect our immune system. This proposal attempts to solve this problem by using advanced genetic techniques to better understand the ways in which immune cells interact with cell-surface sugars. The goal of the project is to identify specific proteins that bind to cancer-associated sugars whose activity can then be blocked for therapeutic purposes.
Program
Project Grant
Location
British Columbia, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
488516
Name
Wisnovsky Simon
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Genetics
Theme2
Biomedical
Prcname2
Genomics: Systems and computational biology
Projecttitle
A systems glycobiology platform for revealing new immunotherapy targets in acute myeloid leukemia
Programtype2
Operating Grants
Orgnameinp2
University of British Columbia
Cihramount2
$887,400
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Acute Myeloid Leukemia; Cancer Immunology; Crispr Screening; Functional Genomics; Glycan-Binding Receptors; Glycans; Glycomics; Innate Immune Checkpoints; Macrophages; Phagocytosis
Abstract
All of the cells in our body are coated with different types of sugar molecules. Cells in our immune system have ways of "tasting" these sugars. Some types of sugars taste good to our immune system, signaling that our cells are healthy and that everything is normal. Other sugars (like those attached to invading bacteria, viruses or cancer cells) taste bad to our immune cells, triggering them to activate and try to protect us from disease. Sometimes our cells can become altered in ways that lead them to produce different or abnormal types of sugar molecules on their surface. When this happens, it can lead our immune cells to overlook unhealthy cells (in the case of cancer). Understanding the details of how this happens can help us develop new drugs to treat such diseases. We face the problem, however, that these cellular sugar molecules are not like the sugar that we eat. Cellular sugars are notoriously chemically complex, making it difficult to predict exactly how specific types of sugar molecules will affect our immune system. This proposal attempts to solve this problem by using advanced genetic techniques to better understand the ways in which immune cells interact with cell-surface sugars. The goal of the project is to identify specific proteins that bind to cancer-associated sugars whose activity can then be blocked for therapeutic purposes.
Competitiondate
202309
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Wisnovsky, Simon
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $887,400~ $0~