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Abstract 2200: The mesenchymal state drives stemness and limits differentiation in glioblastoma.
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Abstract
Glioblastoma is a highly heterogeneous and lethal brain cancer with limited therapeutic options. Recent single-cell omics studies have emphasized the importance of the proneural-mesenchymal axis and strengthened the link between glioblastoma and neurodevelopment, yet the identity and regulatory drivers of glioblastoma stem cells remain poorly defined. In this work, we combined published single-cell datasets with in vitro models to investigate glioblastoma stemness and the tumor’s response to differentiation cues. Through integrative analysis of single-cell RNA sequencing and single-nucleus ATAC sequencing, we refined the landscape of glioblastoma cellular states. Comparison with human subventricular zone profiles reveals a striking similarity between a mesenchymal-like subpopulation and adult radial glia. We further established a comprehensive differentiation assay incorporating phenotypic, transcriptomic, and proteomic readouts. Using this system, we show that glioblastoma cells exhibit heterogeneous responses to differentiation signals and that mesenchymal-like cells, in particular, display pronounced resistance to lineage commitment. Together, these findings highlight the mesenchymal state as a key barrier to differentiation in glioblastoma and lay the groundwork for targeting its underlying drivers to restore differentiation capacity and potentially improve therapeutic outcomes.
Citation Format:
Emanuele Filiberto Rosatti, Denise Sighel, Anna Veronese, Toma Tebaldi, Alessandro Quattrone. The mesenchymal state drives stemness and limits differentiation in glioblastoma [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 2200.
American Association for Cancer Research (AACR)
Title: Abstract 2200: The mesenchymal state drives stemness and limits differentiation in glioblastoma.
Description:
Abstract
Glioblastoma is a highly heterogeneous and lethal brain cancer with limited therapeutic options.
Recent single-cell omics studies have emphasized the importance of the proneural-mesenchymal axis and strengthened the link between glioblastoma and neurodevelopment, yet the identity and regulatory drivers of glioblastoma stem cells remain poorly defined.
In this work, we combined published single-cell datasets with in vitro models to investigate glioblastoma stemness and the tumor’s response to differentiation cues.
Through integrative analysis of single-cell RNA sequencing and single-nucleus ATAC sequencing, we refined the landscape of glioblastoma cellular states.
Comparison with human subventricular zone profiles reveals a striking similarity between a mesenchymal-like subpopulation and adult radial glia.
We further established a comprehensive differentiation assay incorporating phenotypic, transcriptomic, and proteomic readouts.
Using this system, we show that glioblastoma cells exhibit heterogeneous responses to differentiation signals and that mesenchymal-like cells, in particular, display pronounced resistance to lineage commitment.
Together, these findings highlight the mesenchymal state as a key barrier to differentiation in glioblastoma and lay the groundwork for targeting its underlying drivers to restore differentiation capacity and potentially improve therapeutic outcomes.
Citation Format:
Emanuele Filiberto Rosatti, Denise Sighel, Anna Veronese, Toma Tebaldi, Alessandro Quattrone.
The mesenchymal state drives stemness and limits differentiation in glioblastoma [abstract].
In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA.
Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 2200.
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