Englander Institute for Precision Medicine

Multi-scale signaling and tumor evolution in high-grade gliomas.

TitleMulti-scale signaling and tumor evolution in high-grade gliomas.
Publication TypeJournal Article
Year of Publication2024
AuthorsLiu J, Cao S, Imbach KJ, Gritsenko MA, Lih T-SM, Kyle JE, Yaron-Barir TM, Binder ZA, Li Y, Strunilin I, Wang Y-T, Tsai C-F, Ma W, Chen L, Clark NM, Shinkle A, Deen NNaser Al, Caravan W, Houston A, Simin FAnjum, Wyczalkowski MA, Wang L-B, Storrs E, Chen S, Illindala R, Li YD, Jayasinghe RG, Rykunov D, Cottingham SL, Chu RK, Weitz KK, Moore RJ, Sagendorf T, Petyuk VA, Nestor M, Bramer LM, Stratton KG, Schepmoes AA, Couvillion SP, Eder J, Kim Y-M, Gao Y, Fillmore TL, Zhao R, Monroe ME, Southard-Smith AN, Li YE, Lu RJui-Hsien, Johnson JL, Wiznerowicz M, Hostetter G, Newton CJ, Ketchum KA, Thangudu RR, Barnholtz-Sloan JS, Wang P, Fenyö D, An E, Thiagarajan M, Robles AI, Mani DR, Smith RD, Porta-Pardo E, Cantley LC, Iavarone A, Chen F, Mesri M, Nasrallah MLP, Zhang H, Resnick AC, Chheda MG, Rodland KD, Liu T, Ding L
Corporate AuthorsPhiladelphia Coalition for a Cure, Clinical Proteomic Tumor Analysis Consortium
JournalCancer Cell
Volume42
Issue7
Pagination1217-1238.e19
Date Published2024 Jul 08
ISSN1878-3686
KeywordsBrain Neoplasms, Gene Expression Regulation, Neoplastic, Glioblastoma, Glioma, Humans, Isocitrate Dehydrogenase, Mutation, Neoplasm Grading, Phosphorylation, Protein Processing, Post-Translational, Protein Tyrosine Phosphatase, Non-Receptor Type 11, Proteomics, Signal Transduction
Abstract

Although genomic anomalies in glioblastoma (GBM) have been well studied for over a decade, its 5-year survival rate remains lower than 5%. We seek to expand the molecular landscape of high-grade glioma, composed of IDH-wildtype GBM and IDH-mutant grade 4 astrocytoma, by integrating proteomic, metabolomic, lipidomic, and post-translational modifications (PTMs) with genomic and transcriptomic measurements to uncover multi-scale regulatory interactions governing tumor development and evolution. Applying 14 proteogenomic and metabolomic platforms to 228 tumors (212 GBM and 16 grade 4 IDH-mutant astrocytoma), including 28 at recurrence, plus 18 normal brain samples and 14 brain metastases as comparators, reveals heterogeneous upstream alterations converging on common downstream events at the proteomic and metabolomic levels and changes in protein-protein interactions and glycosylation site occupancy at recurrence. Recurrent genetic alterations and phosphorylation events on PTPN11 map to important regulatory domains in three dimensions, suggesting a central role for PTPN11 signaling across high-grade gliomas.

DOI10.1016/j.ccell.2024.06.004
Alternate JournalCancer Cell
PubMed ID38981438

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