Sun Ping, Feng Shunkang, Yu Hui, Wang Xiaoxiao, Fang Yiru
Clinical Research Center, Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai 200030, China.
Qingdao Mental Health Center, Qingdao, Shandong Province 266034, China.
IBRO Neurosci Rep. 2024 Jul 21;17:122-130. doi: 10.1016/j.ibneur.2024.07.006. eCollection 2024 Dec.
Bipolar disorder is a mood illness that affects many people. It has a high recurrence frequency and will cause significant damage to the patient's social function. At present, the pathogenesis of BD is not clear. The National Center for Biotechnology Information (NCBI) established and maintained the Gene Expression Omnibus (GEO) database, a gene expression database. For bioinformatics analysis, researchers can obtain expression data from the internet. At present, the samples of the dataset used in the research of BD are mostly from brain tissue, and the data containing blood samples are rarely used. GEO databases (GSE46416, GSE5388, and GSE5389) were used to retrieve public data, and utilizing the online tool GEO2R, differentially expressed genes (DEGs) were retrieved. The common DEGs between the samples of patients with BD and the samples of the normal population were screened by Venn diagrams. Gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses were used to perform functional annotation and pathway enrichment analysis of DEGs. A protein-protein interaction network (PPI) was built to investigate hub genes on this basis. There were 117 up-regulated DEGs and 38 down-regulated DEGs discovered, with two hub genes [SRC, CDKN1A] among the up-regulated DEGs. These two hub genes were also highly enriched in the oxytocin signaling pathway, proteoglycans in cancer and bladder cancer, according to KEGG analysis. The results of the receiver operating characteristic curve (ROC) of SRC and CDKN1A in the three datasets strongly suggested that SRC and CDKN1A were potential diagnostic markers of BD. The results strongly suggest that SRC and CDKN1A are related to the pathogenesis of BD.
双相情感障碍是一种影响许多人的情绪疾病。它具有高复发率,会对患者的社会功能造成重大损害。目前,双相情感障碍的发病机制尚不清楚。美国国立生物技术信息中心(NCBI)建立并维护了基因表达综合数据库(GEO),这是一个基因表达数据库。对于生物信息学分析,研究人员可以从互联网上获取表达数据。目前,双相情感障碍研究中使用的数据集样本大多来自脑组织,含血样的数据很少被使用。利用GEO数据库(GSE46416、GSE5388和GSE5389)检索公共数据,并使用在线工具GEO2R检索差异表达基因(DEG)。通过维恩图筛选双相情感障碍患者样本与正常人群样本之间的共同DEG。使用基因本体论(GO)和京都基因与基因组百科全书(KEGG)分析对DEG进行功能注释和通路富集分析。在此基础上构建蛋白质-蛋白质相互作用网络(PPI)以研究枢纽基因。共发现117个上调的DEG和38个下调的DEG,上调的DEG中有两个枢纽基因[SRC、CDKN1A]。根据KEGG分析,这两个枢纽基因在催产素信号通路、癌症中的蛋白聚糖和膀胱癌中也高度富集。SRC和CDKN1A在三个数据集中的受试者工作特征曲线(ROC)结果强烈表明,SRC和CDKN1A是双相情感障碍的潜在诊断标志物。结果强烈表明,SRC和CDKN1A与双相情感障碍的发病机制有关。