Recent studies have highlighted the critical role of the mTORC1 pathway in the recurrence and progression of IDH-mutant gliomas. Wang et al. utilized multi-dimensional differential enrichment and spatial transcriptomics to demonstrate that mTORC1 activation correlates with an increased proportion of M2 macrophages, termed Angio-TAMs, which are associated with tumor aggressiveness (ref: Wang doi.org/10.1111/cns.70371/). Furthermore, the CONTIN sign, identified by Wang in a separate study, serves as a predictive imaging biomarker for IDH-mutant gliomas, showing a prevalence of 90.1% in a cohort of gliomas, thus enhancing diagnostic protocols when integrated with other imaging features (ref: Wang doi.org/10.3171/2024.11.JNS242017/). In addition, the expression of DNA methylation machinery (DNMTs and TETs) was investigated by Sufiyan, revealing that while these markers are correlated with tumor grading, they do not independently predict patient survival, indicating a complex interplay of molecular factors influencing outcomes (ref: Sufiyan doi.org/10.1007/s11060-025-05032-x/). Lastly, Kusunoki's research on imaging techniques demonstrated that combining amide proton transfer-weighted imaging with methionine PET significantly enhances the prediction of IDH mutations, underscoring the importance of integrating advanced imaging modalities in glioma diagnostics (ref: Kusunoki doi.org/10.1186/s41824-025-00248-6/).