Recent research has focused on the identification of prognostic biomarkers in glioma, particularly through the lens of RNA modifications. A notable study explored the role of 7-methylguanosine (m7G), a significant RNA modification, in glioma. This study utilized a multi-omics approach to analyze the expression patterns of m7G regulators and their implications for tumor immune microenvironments (TIMEs) and alternative splicing events (ASEs). The findings revealed that dysregulation of m7G is associated with glioma progression, highlighting its potential as a prognostic biomarker. The study emphasizes the importance of understanding the molecular underpinnings of glioma, as the immune landscape and splicing mechanisms are critical for tumor behavior and patient outcomes (ref: Wang doi.org/10.3389/fcell.2022.902394/). This research contributes to the growing body of evidence linking RNA modifications to cancer biology, suggesting that m7G could serve as a valuable target for therapeutic intervention and patient stratification in glioma management. Furthermore, the integration of multi-omics data provides a comprehensive view of glioma biology, paving the way for future studies to explore the clinical utility of m7G signatures in predicting patient prognosis.