Jia Yujie, Nie Kun, Li Jing, Liang Xinyue, Zhang Xuezhu
Institute of Acupuncture and Moxibustion, First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin 300193, P.R. China.
Personnel Department, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, P.R. China.
Mol Med Rep. 2016 Nov;14(5):4844-4848. doi: 10.3892/mmr.2016.5828. Epub 2016 Oct 12.
In order to investigate the pathogenic targets and associated biological process of Alzheimer's disease in the present study, mRNA expression profiles (GSE28146) and microRNA (miRNA) expression profiles (GSE16759) were downloaded from the Gene Expression Omnibus database. In GSE28146, eight control samples, and Alzheimer's disease samples comprising seven incipient, eight moderate, seven severe Alzheimer's disease samples, were included. The Affy package in R was used for background correction and normalization of the raw microarray data. The differentially expressed genes (DEGs) and differentially expressed miRNAs were identified using the Limma package. In addition, mRNAs were clustered using weighted gene correlation network analysis, and modules found to be significantly associated with the stages of Alzheimer's disease were screened out. The Database for Annotation, Visualization, and Integrated Discovery was used to perform Gene Ontology and Kyoto Encyclopedia of Genes and Genomes pathway analyses. The target genes of the differentially expressed miRNAs were identified using the miRWalk database. Compared with the control samples, 175,59 genes and 90 DEGs were identified in the incipient, moderate and severe Alzheimer's disease samples, respectively. A module, which contained 1,592 genes was found to be closely associated with the stage of Alzheimer's disease and biological processes. In addition, pathways associated with Alzheimer's disease and other neurological diseases were found to be enriched in those genes. A total of 139 overlapped genes were identified between those genes and the DEGs in the three groups. From the miRNA expression profiles, 189 miRNAs were found differentially expressed in the samples from patients with Alzheimer's disease and 1,647 target genes were obtained. In addition, five overlapped genes were identified between those 1,647 target genes and the 139 genes, and these genes may be important pathogenic targets for Alzheimer's disease. Through bioinformatics analysis, potential therapeutic targets and associated biological processes were identified, which may assist in understanding and treatment of Alzheimer's disease.
为了在本研究中探究阿尔茨海默病的致病靶点及相关生物学过程,从基因表达综合数据库下载了mRNA表达谱(GSE28146)和微小RNA(miRNA)表达谱(GSE16759)。在GSE28146中,包含8个对照样本以及阿尔茨海默病样本,其中阿尔茨海默病样本包括7个早期、8个中期、7个晚期阿尔茨海默病样本。使用R语言中的Affy包对原始微阵列数据进行背景校正和标准化。使用Limma包鉴定差异表达基因(DEG)和差异表达miRNA。此外,使用加权基因共表达网络分析对mRNA进行聚类,并筛选出与阿尔茨海默病阶段显著相关的模块。使用注释、可视化和综合发现数据库进行基因本体论和京都基因与基因组百科全书通路分析。使用miRWalk数据库鉴定差异表达miRNA的靶基因。与对照样本相比,在早期、中期和晚期阿尔茨海默病样本中分别鉴定出17559个基因和90个DEG。发现一个包含1592个基因的模块与阿尔茨海默病阶段和生物学过程密切相关。此外,发现与阿尔茨海默病和其他神经疾病相关的通路在这些基因中富集。在这些基因与三组中的DEG之间共鉴定出139个重叠基因。从miRNA表达谱中,发现189个miRNA在阿尔茨海默病患者样本中差异表达,并获得1647个靶基因。此外,在这1647个靶基因与139个基因之间鉴定出5个重叠基因,这些基因可能是阿尔茨海默病重要的致病靶点。通过生物信息学分析,鉴定出潜在的治疗靶点及相关生物学过程,这可能有助于阿尔茨海默病的理解和治疗。