Recent studies have focused on innovative targeted therapies for meningiomas, particularly emphasizing the role of specific biomarkers and therapeutic agents. One significant finding is the identification of mesothelin as a promising target for CAR T-cell therapy in meningiomas. This study demonstrated that mesothelin is expressed on the surface of human meningioma cells, suggesting that CAR T-cells engineered to target this antigen could be effective in treating refractory cases (ref: Ramapriyan doi.org/10.1093/neuonc/). Additionally, single-cell analysis has revealed a complex evolutionary trajectory of meningioma cells, highlighting their intra-tumoral heterogeneity and interactions with immune cells, which may influence treatment responses and recurrence rates (ref: Lee doi.org/10.1038/s41467-025-60653-0/). Furthermore, novel therapeutic approaches utilizing microRNA-34a-5p have shown promise in inducing apoptosis in malignant meningioma cells, indicating a potential avenue for future treatment strategies (ref: Ishikawa doi.org/10.1007/s11060-025-05172-0/). The role of Ki-67 as a proliferation marker has also been scrutinized, revealing its complex relationship with immune infiltration in the tumor microenvironment, which could affect prognostic assessments and treatment decisions (ref: Guo doi.org/10.3171/2025.4.JNS25438/). Lastly, the overexpression of EZH2 has been linked to aggressive behavior in high-grade meningiomas, correlating with poor survival outcomes and increased cell proliferation, thus presenting a potential therapeutic target (ref: Szőke doi.org/10.1093/noajnl/).