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胶质母细胞瘤脂质代谢相关基因的生物信息学分析OA

Bioinformatics analysis of lipid metabolism-related genes in glioblastoma

中文摘要英文摘要

目的 利用生物信息学方法鉴定与胶质母细胞瘤(GBM)相关的脂质代谢基因.方法 从基因表达数据库(GEO)获取GSE68848数据集,筛选差异表达基因(DEGs),然后与脂质代谢相关基因交叉.采用基因本体论及京都基因和基因组百科全书分析研究脂质代谢相关DEGs的功能.通过蛋白质-蛋白质相互作用网络进一步确定中枢基因.基因表达谱交互式分析数据库进行验证.基因富集分析用于分析关键中枢基因显著富集的信号通路.肿瘤免疫估计资源数据库评估关键中枢基因表达与免疫细胞浸润之间的相关性.通过"reshape2"软件包和ESTIMATE评分法分析关键中枢基因与免疫检查点、基质评分、免疫评分和ESTIMATE评分之间的相关性.结果 148个脂质代谢相关DEGs中有两个被鉴定为关键中枢基因.富集分析表明,脂质代谢相关DEGs显著调节各种脂质代谢过程.通过MCODE和MCC算法分别鉴定1个关键模块和10个关键中枢基因.CYP27A1、HSD3B7被鉴定为关键中枢基因,并且均与GBM不良预后相关.免疫分析表明,CYP27A1、HSD3B7与多种免疫细胞、多种免疫检查点、基质评分、免疫评分和ESTIMATE评分相关.结论 CYP27A1、HSD3B7被鉴定为可能参与GBM的关键脂质代谢相关基因,为探索GBM的发病机制和潜在治疗靶点提供了新的见解和视角.

Objective To identify glioblastoma(GBM)-related lipid metabolism genes using bioinformatics methods.Methods The GSE68848 dataset was obtained from the Gene Expression Omnibus(GEO)database,and differential expression genes(DEGs)were screened and then intersected with lipid metabolism-related genes.Gene Ontology and Kyoto Encyclopedia of Genes and Genomes analyses were performed to investigate the functions of lipid metabolism-related DEGs.Hub genes were further identified via protein-protein interaction(PPI)network analysis and validated using the gene expression profiling interactive analysis database.Gene set enrichment analysis was used to analyze the signaling pathways significantly enriched by key hub genes.The tumor immune estimation resource database was applied to evaluate the correlation between the expression of key hub genes and immune cell infiltration.The correlations between key hub genes and immune checkpoints,stromal score,immune score,and ESTIMATE score were analyzed using the"reshape2"package and the ESTIMATE algorithm.Results Two of the 148 lipid metabolism-related DEGs were identified as key hub genes.Enrichment analysis showed that lipid metabolism-related DEGs significantly regulated various lipid metabolism processes.One important module and 10 key hub genes were identified by the MCODE and MCC algorithms,respectively.CYP27A1 and HSD3B7 were identified as key hub genes,both of which were associated with poor prognosis in GBM.Immune analysis revealed that CYP27A1 and HSD3B7 were significantly correlated with various immune cells,multiple immune checkpoints,stromal score,immune score,and ESTIMATE score.Conclusion CYP27A1 and HSD3B7 are identified as key lipid metabolism-related genes that may be involved in GBM,providing novel insights and perspectives for exploring the pathogenesis and potential therapeutic targets of GBM.

王立康;姜旭东;张思楠;王馨笛;韩澳迎;张丽娜

154007 佳木斯大学临床医学院大庆油田总医院检验科大庆油田总医院检验科大庆油田总医院检验科154007 佳木斯大学临床医学院大庆市中医医院检验科

胶质母细胞瘤脂质代谢生物信息学中枢基因

GlioblastomaLipid metabolismBioinformaticsHub gene

《浙江医学》 2026 (5)

511-516,后插4-后插5,8

黑龙江省中医药管理局中医药科研课题项目(ZHY2025-158)

10.12056/j.issn.1006-2785.2026.48.5.2025-800

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