胶质瘤
生物
代谢组学
免疫系统
转录组
蛋白质组学
癌症研究
肿瘤微环境
计算生物学
DPYD公司
生物信息学
遗传学
基因
基因表达
药物遗传学
基因型
作者
Jinsen Zhang,Rui Sun,Yingying Lyu,Chaxian Liu,Ying Liu,Yuan Feng,Minjie Fu,Peter Jih Cheng Wong,Zunguo Du,Tianming Qiu,Yi Zhang,Dongxiao Zhuang,Zhiyong Qin,Yu Yao,Wei Zhu,Tiannan Guo,Wei Hua,Hui Yang,Ying Mao
标识
DOI:10.1038/s41467-024-54352-5
摘要
Gliomas exhibit high heterogeneity and poor prognosis. Despite substantial progress has been made at the genomic and transcriptomic levels, comprehensive proteomic characterization and its implications remain largely unexplored. In this study, we perform proteomic profiling of gliomas using 343 formalin-fixed and paraffin-embedded tumor samples and 53 normal-appearing brain samples from 188 patients, integrating these data with genomic panel information and clinical outcomes. The proteomic analysis uncovers two distinct subgroups: Subgroup 1, the metabolic neural subgroup, enriched in metabolic enzymes and neurotransmitter receptor proteins, and Subgroup 2, the immune subgroup, marked by upregulation of immune and inflammatory proteins. These proteomic subgroups show significant differences in prognosis, tumorigenesis, microenvironment dysregulation, and potential therapeutics, highlighting the critical roles of metabolic and immune processes in glioma biology and patient outcomes. Through a detailed investigation of metabolic pathways guided by our proteomic findings, dihydropyrimidine dehydrogenase (DPYD) and thymidine phosphorylase (TYMP) emerge as potential prognostic biomarkers linked to the reprogramming of nucleotide metabolism. Functional validation in patient-derived glioma stem cells and animal models highlights nucleotide metabolism as a promising therapy target for gliomas. This integrated multi-omics analysis introduces a proteomic classification for gliomas and identifies DPYD and TYMP as key metabolic biomarkers, offering insights into glioma pathogenesis and potential treatment strategies. Comprehensive molecular characterisations could shed light on the high heterogeneity and poor prognosis of gliomas. Here, the authors perform proteomic profiling of 188 glioma patients, revealing immune and metabolic neuron-related subgroups as well as metabolic biomarkers linked to prognosis.
科研通智能强力驱动
Strongly Powered by AbleSci AI