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Quantitative proteomic landscapes of primary and recurrent glioblastoma reveal a protumorigeneic role for FBXO2-dependent glioma-microenvironment interactions.

Marcel Buehler,Xiao Yi,Weigang Ge,P. Blattmann,E. Rushing,G. Reifenberger,J. Felsberg,Charles D. Yeh,Jacob E. Corn,L. Regli,Junyi Zhang,Ann Cloos,V. Ravi,B. Wiestler,D. Heiland,R. Aebersold,M. Weller,T. Guo,T. Weiss

Published 2022 in Neuro-Oncology

ABSTRACT

BACKGROUND Recent efforts have described the evolution of glioblastoma from initial diagnosis to post-treatment recurrence on a genomic and transcriptomic level. However, the evolution of the proteomic landscape is largely unknown. METHODS Sequential window acquisition of all theoretical mass spectra mass spectrometry (SWATH-MS) was used to characterize the quantitative proteomes of two independent cohorts of paired newly diagnosed and recurrent glioblastomas. Recurrence-associated proteins were validated using immunohistochemistry and further studied in human glioma cell lines, orthotopic xenograft models and human organotypic brain slice cultures. External spatial transcriptomics, single-cell- and bulk RNA sequencing data was analyzed to gain mechanistical insights. RESULTS Although overall proteomic changes were heterogeneous across patients, we identified BCAS1, INF2 and FBXO2 as consistently upregulated proteins at recurrence and validated these using immunohistochemistry. Knockout of FBXO2 in human glioma cells conferred a strong survival benefit in orthotopic xenograft mouse models and reduced invasive growth in organotypic brain slice cultures. In glioblastoma patient samples, FBXO2 expression was enriched in the tumor infiltration zone and FBXO2-positive cancer cells were associated with synaptic signaling processes. CONCLUSIONS These findings demonstrate a potential role of FBXO2-dependent glioma-microenvironment interactions to promote tumor growth. Furthermore, the published datasets provide a valuable resource for further studies.

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