Meningiomas are the most common non-malignant intracranial tumors, and their biology and genetics are critical for understanding their behavior and treatment. One study highlights the role of human endogenous retrovirus type K in promoting proliferation and sensitivity to antiretroviral drugs in Merlin-negative tumors, suggesting a potential therapeutic target (ref: Maze doi.org/10.1158/0008-5472.CAN-20-3857/). Another investigation into glycation processes in meningiomas reveals that anaerobic glycolysis leads to increased levels of methylglyoxal, which may interfere with sialyltransferase expression, potentially impacting tumor progression (ref: Selke doi.org/10.3390/cells10123298/). Furthermore, a study correlating MTAP immunohistochemistry with CDKN2A status indicates that MTAP loss may serve as a prognostic marker for meningiomas, particularly in atypical and anaplastic cases (ref: Sasaki doi.org/10.1093/jnen/). Whole-exome sequencing of sporadic WHO grade 1 meningiomas has uncovered heterogeneous mutational profiles, emphasizing the need for personalized treatment approaches (ref: González-Tablas doi.org/10.3389/fonc.2021.740782/). Lastly, a growth analysis of untreated meningiomas under observation provides insights into their growth patterns, with initial volumes averaging 2.44 mL, which is crucial for clinical decision-making (ref: Opalak doi.org/10.1055/s-0041-1739216/).