Recent studies have significantly advanced our understanding of the molecular and genetic landscape of meningiomas, revealing distinct subtypes with varying prognostic implications. Choudhury et al. identified three major DNA methylation groups: Merlin-intact meningiomas, which represent 34% of cases and show the best outcomes due to NF2/Merlin regulation, immune-enriched meningiomas at 38% with intermediate outcomes characterized by immune infiltration, and hypermitotic meningiomas at 28% that exhibit the worst outcomes due to genetic and epigenetic mechanisms driving cell cycle dysregulation and resistance to therapy (ref: Choudhury doi.org/10.1038/s41588-022-01061-8/). Furthermore, Slavik et al. introduced Lnc-GOLGA6A-1 as a novel prognostic biomarker for meningioma recurrence, emphasizing the need for reliable biomarkers to predict tumor behavior and guide treatment (ref: Slavik doi.org/10.1227/neu.0000000000002026/). Wang et al. utilized single-cell RNA sequencing to explore the cellular landscape of meningiomas and the human dura, providing insights into immune responses that could inform therapeutic strategies (ref: Wang doi.org/10.1186/s13073-022-01051-9/). Additionally, Deng et al. highlighted the potential of FK866, a nicotinamide phosphoribosyltransferase inhibitor, in suppressing anaplastic meningioma growth and inhibiting immune checkpoint expression, suggesting new avenues for targeted therapy (ref: Deng doi.org/10.3389/fonc.2022.836257/). These findings collectively underscore the heterogeneity of meningiomas and the importance of molecular profiling in developing personalized treatment approaches.