Recent studies have focused on identifying biomarkers and understanding the molecular mechanisms underlying meningiomas. One significant finding is that targeted gene expression profiling can effectively stratify clinical low-risk meningiomas, with 51.3% classified as molecular intermediate-risk and 9.5% as molecular high-risk, indicating a potential for recurrence post-surgery (ref: Nguyen doi.org/10.1093/neuonc/). Additionally, the role of the NF2/Merlin pathway has been explored, revealing that about one-third of meningiomas with favorable outcomes retain Merlin expression, suggesting that biochemical mechanisms in Merlin-intact tumors remain poorly understood (ref: Eaton doi.org/10.1038/s41467-024-52284-8/). Furthermore, a quantitative analysis identified protein signatures, specifically AK2, COL1A1, and PLG, which may serve as targeted therapeutic avenues for meningioma treatment (ref: Sharma doi.org/10.1097/JS9.0000000000002054/). The metabolic characteristics of meningiomas have also been investigated, with findings indicating that glucose levels and glycation significantly influence tumor cell migration and invasion, linking metabolic alterations to cancer hallmarks (ref: Selke doi.org/10.3390/ijms251810075/). Overall, these studies highlight the complexity of meningioma biology and the potential for developing novel diagnostic and therapeutic strategies based on molecular profiling and metabolic pathways.