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Berglund, M.

Publications and source records attributed to Berglund, M..

2 recordsLinked to original sources

Reconstructing the Single-Cell Spatiotemporal Dynamics of Glioblastoma Invasion

Glioblastoma invasion into healthy brain tissue remains a major barrier to effective treatment, yet current models fail to capture its full complexity in a scalable and patient-specific manner. Here, we introduce GlioTrace, a novel ex vivo imaging and AI-based analytical framework that enables real-time, spatiotemporal tracking of glioblastoma invasion dynamics in patient-derived glioma cell culture xenograft (PDCX) brain slices. By integrating whole-specimen confocal microscopy, vascular counterstaining, and an advanced computational pipeline combining convolutional neural networks and Hidden Markov Models, GlioTrace identifies distinct invasion modes, including dynamic morphological switching, vessel-guided migration, and immune cell interactions and quantifies patient-specific variations in invasion plasticity. Using GlioTrace, we demonstrate that targeted therapies can selectively modulate invasion phenotypes, revealing spatially and temporally distinct drug responses. This scalable platform provides an unprecedented window into glioblastoma progression and treatment response, offering a powerful tool for precision oncology and anti-invasion therapeutic development.

cancer biology↗

The invasion phenotypes of glioblastoma depend on plastic and reprogrammable cell states

Glioblastoma (GBM), the most common primary brain cancer in adults, is characterized by rapid local invasion along diverse routes, such as infiltration of white matter tracts and penetration of perivascular spaces. We investigate the hypothesis that GBM invasion routes correlate with the transcriptional states of individual cells and identify regulators of route-specific invasion. Utilizing patient-derived GBM xenograft models, we integrate single-cell transcriptomics and spatial proteomics, revealing that mesenchymal and oligodendrocyte progenitor-like GBM cells migrate perivascularly, while neural progenitor and astrocyte-like GBM cells invade diffusely. Computational reconstruction identifies ANXA1 as a perivascular invasion driver and lineage-restricted transcription factors RFX4 and HOPX as drivers of diffuse invasion, predictive of patient survival. Genetic ablation of these genes alters invasion phenotypes and extends survival in xenografted mice, clarifying the role of cell states in GBM invasion, and highlighting potential therapeutic targets for selective invasion route targeting in GBM patients.

cancer biology↗