Recent advancements in spatial transcriptomics have significantly enhanced our understanding of gliomas, particularly in identifying the cellular composition and microenvironmental influences on tumor behavior. One study revealed that in diffuse midline glioma-H3K27M mutant (DMG) and glioblastoma (GBM), radial glial stem-like (RG-like) cells were predominantly found in the neuron-rich invasive niches, contrasting with the tumor core, which was enriched with oligodendrocyte precursor-like cells. This study not only identified niche-specific regulatory programs for RG-like cells but also functionally confirmed the role of FAM20C in mediating their invasive growth within a neuron-rich microenvironment, highlighting the complexity of glioma biology (ref: Ren doi.org/10.1038/s41467-023-36707-6/). Furthermore, another investigation utilized an integrated multimodal approach combining NanoString GeoMx Digital Spatial Profiling and single-cell RNA-seq to analyze archival glioblastoma specimens. This innovative methodology allowed for a comprehensive characterization of the spatial distribution of molecular and cellular therapeutic targets within the glioblastoma microenvironment, demonstrating the potential of spatial biology in elucidating tumor heterogeneity (ref: Kim doi.org/10.1016/j.modpat.2022.100034/). Together, these studies underscore the importance of spatial context in glioma research and the potential for targeted therapeutic strategies based on microenvironmental interactions.