首页|肝细胞癌和动脉粥样硬化共表达基因的筛选和验证

肝细胞癌和动脉粥样硬化共表达基因的筛选和验证

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目的 通过生物信息学分析鉴定肝细胞癌(Hepatocellular carcinoma,HCC)与动脉粥样硬化(Atherosclerosis,AS)的共表达基因.方法 下载基因表达数据库(Gene expression om-nibus,GEO)中肝细胞癌(GSE84402,GSE25097)和动脉粥样硬化(GSE28829,GSE100927)的数据集.使用R软件加权基因共表达网络分析(Weighted gene co-expression networkanalysis,WGC-NA)分析GSE84402和GSE28829数据集中共表达基因,Limma鉴定GSE25097和GSE100927数据集中差异表达基因(Differential gene express,DEGs),使用Venny识别WGCNA与差异基因的共表达基因并使用clusterProfiler进行、基因本体(Gene ontology,GO分析和基因组百科全书(Kyoto encyclopedia of genes and genomes,KEGG)分析.对WGCNA和差异基因的共表达基因进行qPCR,免疫组织化学技术(Immunohistochemistry,IHC),免疫荧光共定位(Immunofluores-cence,IF)等实验验证.结果 WGCNA分析共识别227个共表达基因,差异基因表达分析共识别5个共表达基因,鉴定HIF1A、CASP8、LEF1、BCAT1、LPL为HCC与AS共表达基因,KEGG分析显示这些基因主要富集在细胞周期和 MAPK信号通路,在HCC和AS中qPCR、IHC、免疫荧光共定位(Immunofluorescence,IF)均显示,共表达基因在病灶组织中的表达均高于对照组织(P<0.05).结论 HIF1A、CASP8、LEF1、BCAT1、LPL 5个共表达基因可能是HCC与AS的潜在生物学标志物.同时,MAPK信号通路及细胞周期通路在HCC和AS的发生发展中起到关键作用.
Screening and validation of co-expressed genes in hepatocellular carcinoma(HCC)and atherosclerosis(AS)
Objective Identification of co-expressed genes in hepatocellular carcinoma(HCC)and athero-sclerosis(AS)by bioinformatics analysis.Methods The datasets of hepatocellular carcinoma(GSE84402,GSE25097)and atherosclerosis(GSE28829,GSE100927)were downloaded from the gene expression om-nibus(GEO)database.Co-expressed genes in GSE84402 and GSE28829 datasets were analyzed using the R software weighted gene co-expression networkanalysis(WGCNA)package,and it differentially expressed genes(differential gene express,DEGs)in GSE25097 and GSE100927 datasets were identified using the"Limma"package.Co-expressed genes in WGCNA and differential genes were identified using Venny and(gene ontology)GO enrichment analysis and(genome encyclopedia)KEGG analysis were per-formed using the"clusterProfiler"package.The co-expressed genes of WGCNA and differential genes were verified by qPCR,immunohistochemistry(IHC)and immunofluorescence(IF).Results A total of 227 co-expressed genes were identified by WGCNA analysis,and 5 co-expressed genes were identified by differential gene expression analysis.HIF1A,CASP8,LEF1,BCAT1 and LPL were identified as co-ex-pressed genes in HCC and AS,and KEGG analysis showed that the genes were mainly enriched in the cell cycle and MAPK signaling pathway.qPCR,IHC and IF were all shown to be in HCC and AS,and the ex-pression of co-expressed genes were higher than that in control tissues in the lesion tissues(P<0.05).Conclusion Bioinformatics screened 5 co-expressed genes of HIF1A,CASP8,LEF1,BCAT1 and LPL,which may be potential biological markers for HCC and AS,as well as the MAPK signaling pathway and cell cycle pathway plays key roles in the development of hepatocellular carcinoma and atherosclerosis.

hepatocellular carcinoma(HCC)atherosclerosis(AS)bioinformaticsgene expression omnibus

马玉玉、张丽、王炫峥、乃菲沙·买买提、米叶沙尔·安尼娃尔、马秀敏

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新疆医科大学 第三临床医学院/附属肿瘤医院, 乌鲁木齐 830011

新疆医科大学 第一附属医院检验科, 乌鲁木齐 830011

肝细胞癌 动脉粥样硬化 生物信息学 基因表达数据库

新疆维吾尔自治区产学合作协同育人项目

2024

新疆医科大学学报
新疆医科大学

新疆医科大学学报

CSTPCD
影响因子:0.76
ISSN:1009-5551
年,卷(期):2024.47(3)
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