Recent studies have significantly advanced our understanding of the genetic and molecular landscape of meningiomas, particularly focusing on the role of TERT mutations and BAP1 deficiency. One study analyzed TERT expression in meningiomas, revealing that grade 1 tumors with TERT expression had a progression-free survival (PFS) comparable to TERT-negative grade 2 tumors, while grade 2 tumors with TERT expression showed similar PFS to TERT-negative grade 3 tumors (ref: Gui doi.org/10.1016/S1470-2045(25)00267-0/). Another investigation found that 4.73% of meningiomas were TERTp-mutant, with a median age of 67 years for affected patients, highlighting demographic differences in tumor types (ref: Groff doi.org/10.1016/S1470-2045(25)00422-X/). Furthermore, BAP1-deficient meningiomas, often associated with a high risk of relapse, were identified through specific methylation classes, indicating the need for careful histomolecular diagnosis (ref: Drabent doi.org/10.1111/nan.70042/). The identification of circRNA and its correlation with clinical features in recurrent grade 2 meningiomas adds another layer to the molecular understanding, suggesting that circPIM1 may play a role in tumor recurrence (ref: Sotera doi.org/10.3390/ijms26178263/). Additionally, NOTCH3's involvement in fatty acid oxidation and ferroptosis resistance in aggressive meningiomas underscores its potential as a therapeutic target (ref: Sadagopan doi.org/10.1007/s11060-025-05208-5/). Lastly, functional connectivity alterations in patients with olfactory groove meningiomas were observed using resting-state fMRI, indicating the broader implications of meningiomas on brain networks (ref: Filimonova doi.org/10.3389/fneur.2025.1644138/).