Recent studies have focused on the molecular and genetic profiling of meningiomas, revealing significant insights into their classification and progression. Ricklefs et al. conducted genetic and epigenetic profiling on 65 spinal meningioma samples, identifying two distinct classes based on their molecular characteristics, which could lead to more tailored treatment approaches (ref: Ricklefs doi.org/10.1007/s00401-022-02504-6/). Ng et al. explored the cytogenetic changes in NF2/22q and non-NF2/22q meningiomas, finding that the former exhibited more abnormalities from the outset, while the latter acquired significant changes predominantly at recurrence, highlighting different life histories and potential therapeutic targets (ref: Ng doi.org/10.1111/bpa.13120/). Maier's investigation into gene expression changes during the progression from benign to malignant meningiomas found that specific neuroinflammatory signatures could serve as early indicators of transformation, suggesting that monitoring these changes could improve patient outcomes (ref: Maier doi.org/10.3171/2022.7.JNS22585/). Furthermore, the role of microRNAs in meningioma classification was examined by Abdelrahman et al., who demonstrated that serum levels of miR-497 and miR-219 could effectively differentiate between tumor grades, indicating their potential as non-invasive biomarkers (ref: Abdelrahman doi.org/10.1007/s11060-022-04126-0/). These findings collectively underscore the importance of molecular profiling in understanding meningioma biology and improving diagnostic and therapeutic strategies.