CSIG-36. LEVERAGING GENOMIC ALTERATIONS IN GLIOBLASTOMA MULTIFORME

Abstract In GBM, the most common genomic events include chromosome 7 gain, chromosome 9p loss, or chromosome 10 loss. At least 80% of GBM tumors have one or more of these chromosome alterations. Since these gains and losses involve entire chromosome arms, we predict that more than one gene on each arm functions to promote tumorigenesis. Using a combination of computational studies and chromosome-specific CRISPR screens, we identified a novel oncogene on chromosome 7 and two novel haploinsufficient tumor suppressor genes on chromosomes 9p and 10.

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Publication Details

Journal
Neuro-Oncology
Published
2025-11-01
DOI
https://doi.org/10.1093/neuonc/noaf201.0370
Primary Topic
Chromatin Remodeling and Cancer
Type
article
Field-Weighted Citation Impact
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article

CSIG-36. LEVERAGING GENOMIC ALTERATIONS IN GLIOBLASTOMA MULTIFORME

Neil McGowan, Tamar R. Berger, Keith Lloyd Ligon, Muhannad Abu‐Remaileh et al.
Neuro-Oncology
Chromatin Remodeling and Cancer
article

CSIG-36. LEVERAGING GENOMIC ALTERATIONS IN GLIOBLASTOMA MULTIFORME

Neil McGowan, Tamar R. Berger, Keith Lloyd Ligon, Muhannad Abu‐Remaileh, Rameen Beroukhim, Nitin H. Shirole, Margaret Cusick, William G. Kaelin
article en

Abstract

Abstract In GBM, the most common genomic events include chromosome 7 gain, chromosome 9p loss, or chromosome 10 loss. At least 80% of GBM tumors have one or more of these chromosome alterations. Since these gains and losses involve entire chromosome arms, we predict that more than one gene on each arm functions to promote tumorigenesis. Using a combination of computational studies and chromosome-specific CRISPR screens, we identified a novel oncogene on chromosome 7 and two novel haploinsufficient tumor suppressor genes on chromosomes 9p and 10.

Neuro-OncologyVol. 27(Supplement_5)
Dana-Farber Cancer Institute (US)
Openalex Percentile: Top 70%
Chromatin Remodeling and Cancer
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