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作 者:杨明丽[1] 黄哲[2] 王倩[1] 陈欢欢[1] 马赛男[1] 吴荣[1] 蔡炜嵩[1] YANG Mingli;HUANG Zhe;WANG Qian;CHEN Huanhuan;MA Sainan;WU Rong;CAI Weisong(The 2nd Department of Oncology,Shengjing Hospital,China Medical University,Shenyang 110022,China;Department of General Surgery,Shengjing Hospital,China Medical University,Shenyang 110015,China)
机构地区:[1]中国医科大学附属盛京医院第二肿瘤内科,沈阳110022 [2]中国医科大学附属盛京医院普通外科,沈阳110015
出 处:《中国医科大学学报》2020年第2期134-138,共5页Journal of China Medical University
基 金:辽宁省自然科学基金(20170541001)
摘 要:目的通过生物信息学的方法分析胰腺癌发生的潜在机制。方法利用GEOquery分析差异基因表达,利用clusterProfiler进行富集分析。利用STRING数据库进行蛋白相互作用分析。通过TCGA数据库对核心基因进行预后分析。结果通过差异分析得到277个差异基因。通过富集分析发现,低表达基因主要和胆固醇代谢过程、酒精代谢过程以及消化有关,高表达基因主要和消化系统过程有关。蛋白相互作用分析后找到胰腺癌发生的10个核心基因(ALB、EGF、FN1、COL1A1、COL3A1、ITGA2、COL17A1、CEL、PRSS1和TOP2A)。经过TCGA数据库预后分析发现3个基因(COL17A1、ITGA2、TOP2A)和预后相关。结论发现了10个胰腺癌发病风险相关的核心基因和3个预后相关基因。这些核心基因可能可以作为胰腺癌发病预测的靶标。Objective To analyze the mechanisms underlying pancreatic cancer using bioinformatics methods.Methods GEOquery was used to analyze differential gene expression,and clusterProfiler was used for enrichment analysis.Protein interaction analysis was performed using the STRING database.Prognostic analysis of core genes was performed using TCGA database.Results Based on the differential analysis,277 differentially expressed genes were identified.The enrichment analysis revealed that the low-expression genes were mainly involved in cholesterol metabolism,alcohol metabolism,and digestion,and high-expression genes were mainly related to digestive system processes.Protein interaction analysis identified 10 core genes related to pancreatic cancer(ALB,EGF,FN1,COL1A1,COL3A1,ITGA2,COL17A1,CEL,PRSS1,and TOP2A).After prognostic analysis of TCGA database was performed,three genes(COL17A1,ITGA2,and TOP2A supplemented with specific gene names)were found to be associated with prognosis.Conclusion Ten core genes associated with the risk of pancreatic cancer and three genes related to prognosis were identified.These core genes may serve as targets for the prediction of pancreatic cancer incidence.
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