首页|基于GEO基因数据集的酒精性肝炎差异表达基因生物信息学分析

基于GEO基因数据集的酒精性肝炎差异表达基因生物信息学分析

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目的 利用数据库挖掘寻找调控酒精性肝炎的靶点基因以及基因的调控网络,以期探索酒精性肝炎治疗新方向,对减轻疾病负担提供新思路.方法 检索 GEO数据库,从中获取酒精性肝炎相关表达数据集 GSE143318 和 GSE167308,筛选两个数据集共有的差异表达基因(differentially expressed genes,DEGs),并用GSE28619 基因芯片进行验证.利用生物信息学方法,对DEGs进行分析,研究调控 DEGs的非编码 RNAs.结果 两组数据集筛查出 DEGs共 261 个,GO功能分析主要在类固醇代谢、炎症反应、脂质代谢等 7 个生物学过程,细胞膜及细胞外基质的 6 个细胞组分,还有与肝素结合、生长因子、蛋白酶抑制剂、金属蛋白酶、氧化还原酶等 11 个分子功能.KEGG显示,这些 DEGs主要富集在类固醇激素生物合成、视黄醇代谢、细胞色素 P450 的代谢、细胞外基质受体的相互作用、胆固醇代谢及 PPAR信号通路.通过在 PPI网络中运用不同算法以及 GSE28619 芯片验证,共筛选出 6 个核心差异基因,分别为 SPP1、THBS2、CYP1A1、EPCAM、CXCL8、KRT19.miR-466 表现出与 DEGs 密切的相关性.结论 酒精性肝炎中的DEGs与疾病的发生发展相关,生物信息学技术的方法为更深入研究酒精性肝炎的发病机制和治疗靶点提供新的思路.
Bioinformatics analysis of differentially expressed genes in alcoholic hepatitis based on GEO gene dataset
Objective To search for target genes and gene regulatory networks that regulate alcoholic hepatitis by using database mining,and explore new directions for the treatment of alcoholic hepatitis and provide new ideas for reducing disease burden.Methods Retrieve the GEO database to obtain the alcoholic hepatitis related expression data-sets GSE143318 and GSE167308,screen for differentially expressed genes(DEGs)that were common to both datasets,and validate them using the GSE28619 gene chip.Using bioinformatics methods,analyze DEGs and study the non-coding RNAs that regulate DEGs.Results A total of 261 DEGs were screened from the two data sets.GO function analysis mainly focused on 7 biological processes,including steroid metabolism,inflammatory reaction and lipid metabolism,6 cell components of cell membrane and extracellular matrix,and 11 molecular functions,including heparin binding,growth factors,protease inhibitors,metalloproteinases and oxidoreductase.KEGG showed that these DEGs were mainly enriched in steroid hormone biosynthesis,retinol metabolism,cytochrome P450 metabolism,extracellular matrix recep-tor interaction,cholesterol metabolism and PPAR signaling pathway.By using different algorithms and GSE28619 chip validation in the PPI network,a total of 6 core differential genes were screened,namely SPP1,THBS2,CYP1A1,EPCAM,CXCL8 and KRT19.MiR-466 exhibited a close correlation with DEGs.Conclusion DEGs in alcoholic hepa-titis are related to the occurrence and development of diseases,and the methods of bioinformatics technology provide new ideas for deeper research on the pathogenesis and treatment targets of alcoholic hepatitis.

Alcoholic hepatitisDifferentially expressed genesGEO database

杨润萌、于盈盈、赵美怡、吕文良

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中国中医科学院广安门医院感染疾病科,北京 100053

酒精性肝炎 差异表达基因 GEO数据库

中国中医科学院科技创新工程项目中国中医科学院科技创新工程项目

CI2021A00801CI2021A00802

2024

胃肠病学和肝病学杂志
郑州大学

胃肠病学和肝病学杂志

CSTPCD
影响因子:1.029
ISSN:1006-5709
年,卷(期):2024.33(10)
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