AUTHOR=Kang Jianlei , Xu Yujie , Zhao Qitai , Wang Ying , He Zhenyan , Xu Xin 

TITLE=Metabolic profiling of glioblastoma and identification of G0S2 as a metabolic target

JOURNAL=Frontiers in Oncology

VOLUME=Volume 15 - 2025

YEAR=2025

URL=https://www.frontiersin.org/journals/oncology/articles/10.3389/fonc.2025.1572040

DOI=10.3389/fonc.2025.1572040

ISSN=2234-943X

ABSTRACT=IntroductionMetabolic reprogramming is a hallmark of cancer, yet its role in glioma remains poorly understood. Gliomas are characterized by a highly immunosuppressive tumor microenvironment (TME) and poor prognosis. This study systematically explores the relationship between glioma metabolomics, tumor phenotype, and the immune microenvironment.MethodsBulk RNA sequencing data were retrieved from the Chinese Glioma Genome Atlas (CGGA) and The Cancer Genome Atlas (TCGA). Single-cell gene set enrichment analysis (ssGSEA) was employed to quantify seven nutrient metabolic pathways and immune infiltration. Consensus clustering was applied to group gliomas based on metabolic gene expression, and survival analysis was performed to evaluate survival differences across these clusters. A predictive model was constructed and validated using our cohort. Finally, we knocked out G0S2 in glioma cells and performed RNA sequencing to investigate differentially activated pathways. Additionally, in vivo experiments were conducted to explore the antitumor effects of G0S2 knockout in combination with PD-1 monoclonal antibody.ResultsSignificant metabolic differences were identified between low-grade gliomas (LGG) and glioblastomas (GBM), with consistent findings across both databases. We found that LGGs and GBMs exhibit distinct metabolic patterns. Consensus clustering revealed three metabolic subgroups, with the C3 subgroup demonstrating poor survival and enhanced infiltration of immunosuppressive cells. The predictive model showed robust performance in forecasting the survival of glioma patients. Functional analysis identified G0S2 as a key metabolic regulator highly expressed in gliomas. G0S2 knockout activated the type I interferon signaling pathway, enhanced CD8+ T cell functionality, and synergized with anti-PD-1 therapy, resulting in suppressed tumor growth and prolonged survival in vivo.ConclusionThese findings provide a comprehensive analysis of glioma metabolic patterns and identify G0S2 as a promising therapeutic target.