Recent studies have significantly advanced our understanding of the biological features and molecular mechanisms underlying meningiomas, particularly in relation to tumor aggressiveness. One pivotal study identified tumor-associated macrophages (TAMs) as a critical immune cell population in meningiomas, revealing that higher TAM infiltration correlates with clinically aggressive tumors, suggesting their potential as a prognostic biomarker (ref: Lotsch doi.org/10.1007/s00401-025-02948-6/). Another investigation utilized transcriptomic profiling across different WHO grades of meningiomas, highlighting increased cell proliferation and alterations in cellular metabolism as key features distinguishing aggressive tumors from benign ones (ref: Baluszek doi.org/10.3390/cancers17203324/). Furthermore, the overexpression of CKS2 in high-grade and recurrent meningiomas was linked to its oncogenic role, emphasizing the need for targeted therapies beyond conventional surgical and radiotherapeutic options (ref: Sharma doi.org/10.1016/j.compbiomed.2025.111142/). Additionally, a novel oxidative stress-based molecular classification was proposed to better predict tumor behavior in WHO grade 2/3 meningiomas, addressing the limitations of traditional histopathological grading (ref: Luo doi.org/10.32604/or.2025.066308/). Lastly, the role of gut microbiota in meningioma pathogenesis was explored, revealing potential links between intestinal microbial communities and tumor development through circulating metabolites (ref: Chen doi.org/10.1002/brb3.70973/).