Multi-omic landscape of human gliomas from diagnosis to treatment and recurrence
- PMID: 41386224
- DOI: 10.1016/j.ccell.2025.11.006
Multi-omic landscape of human gliomas from diagnosis to treatment and recurrence
Abstract
Gliomas are among the most lethal cancers, with limited treatment options. To uncover hallmarks of therapeutic escape and tumor microenvironment (TME) landscape, we applied spatial proteomics, transcriptomics, and glycomics to 670 lesions from 310 adult and pediatric patients. Single-cell analysis shows high B7H3+ tumor cell prevalence in glioblastoma (GBM) and pleomorphic xanthoastrocytoma, while most gliomas, including pediatric cases, express targetable tumor antigens in less than 50% of tumor cells, potentially explaining trial failures. Paired samples of isocitrate dehydrogenase (IDH)-mutant gliomas reveal recurrence driven by tumor-immune spatial reorganization, shifting from T cell and vasculature-associated myeloid cell-enriched niches to microglia and CD206+ macrophage-dominated tumors. Multi-omic integration identified N-glycosylation as the best classifier of grade, while the immune transcriptome best predicted GBM survival. Provided as a community resource, this study offers a framework for glioma targeting, classification, outcome prediction, and a baseline of TME composition across all stages.
Keywords: GBM; TME; diffuse midline glioma; glioma; immune regulation; immunotherapy; single-cell profiling; spatial N-glycome; spatial multi-omics; tumor antigens.
Copyright © 2025 Elsevier Inc. All rights reserved.
Conflict of interest statement
Declaration of interests M. Angelo and S.B. are named inventors on patent US20150287578A1, which covers the mass spectrometry approach utilized by MIBI-TOF. M. Angelo and S.B. are board members and shareholders in IonPath, which develops and manufactures the commercial MIBI-TOF platform.
Update of
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Multi-omic landscape of human gliomas from diagnosis to treatment and recurrence.bioRxiv [Preprint]. 2025 Apr 9:2025.03.12.642624. doi: 10.1101/2025.03.12.642624. bioRxiv. 2025. Update in: Cancer Cell. 2026 Jan 12;44(1):112-128.e6. doi: 10.1016/j.ccell.2025.11.006. PMID: 40161803 Free PMC article. Updated. Preprint.
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