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Grant: Project Grant

Ontario Institute for Cancer Research (Toronto, Ontario)

$1,013,626.00

Immunotherapeutic Targeting of the U1 snRNA Mutation in Cancer

FY 2019-20

Summary
We seek funding to explore the development of novel therapeutics targeted against a novel class of driver mutation that we recently discovered in several types of hard-to-treat cancer. This mutation affects the U1 small nuclear RNA, a core component of the spliceosome. It is only the third cancer driver mutation identified in a non-coding RNA, and is present in several difficult-to-treat cancer types, including adult chronic lymphocytic leukemia and pediatric cerebellar medulloblastoma. Tumours carrying this mutation have widespread alterations in splicing, leading to activation of several known or suspected oncogenic pathways. Unlike mutations that affect protein components of the spliceosome, the patterns of mis-splicing in U1 mutant cells are identical from tumour to tumour, raising the possibility of creating an off-the-shelf immunotherapy targeted against the neo-antigens present in U1 mutant tumours. This project brings together a team with expertise in computational biology, proteogenomics, immunotherapy, and the management of adult leukemia and pediatric brain cancer.
Program
Project Grant
Location
Ontario, Canada
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
420493
Name
Stein Lincoln
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Cancer Biology & Therapeutics
Projecttitle
Immunotherapeutic Targeting of the U1 snRNA Mutation in Cancer
Programtype2
Operating Grants
Orgnameinp2
Ontario Institute for Cancer Research (Toronto, Ontario)
Cihramount2
$1,013,626
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Cancer; Computational Biology; Immunotherapy; Non-Coding Rna; Proteomics; Targeted Cancer Therapy
Abstract
We seek funding to explore the development of novel therapeutics targeted against a novel class of driver mutation that we recently discovered in several types of hard-to-treat cancer. This mutation affects the U1 small nuclear RNA, a core component of the spliceosome. It is only the third cancer driver mutation identified in a non-coding RNA, and is present in several difficult-to-treat cancer types, including adult chronic lymphocytic leukemia and pediatric cerebellar medulloblastoma. Tumours carrying this mutation have widespread alterations in splicing, leading to activation of several known or suspected oncogenic pathways. Unlike mutations that affect protein components of the spliceosome, the patterns of mis-splicing in U1 mutant cells are identical from tumour to tumour, raising the possibility of creating an off-the-shelf immunotherapy targeted against the neo-antigens present in U1 mutant tumours. This project brings together a team with expertise in computational biology, proteogenomics, immunotherapy, and the management of adult leukemia and pediatric brain cancer.
Competitiondate
202003
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Stein, Lincoln
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $1,013,626~ $0~