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Identification of Biomarkers Associated With Alzheimer's Disease by Bioinformatics Analysis

机译:通过生物信息学分析鉴定与阿尔茨海默氏病相关的生物标志物

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Background: This study aimed to explore the biomarkers of Alzheimer's disease (AD). Methods: The microarray data of GSE16759 were from the expression profile samples of 4 parietal lobe tissues from patients with AD and 4 ones from age-matched control participants. The differentially expressed micro RNAs (miRNAs) and genes (DEGs) underwent hierarchical clustering and function analysis followed by target genes prediction. Finally, DEGs were mapped to the target genes to construct miRNA-regulated networks. Results: A total of 427 DEGs were obtained and clustered into 5 functions. After DEGs were mapped to the predicted target genes, 313 regulatory pairs were established. The target genes SEC22 vesicle trafficking protein homolog B (SEC22B) and SEC63 homolog (SEC63) regulated by miRNA-206, RAB10, member RAS oncogene family (RAB10) regulated by miRNA-655, and fms-related tyrosine kinase 1 (FLT1) regulated by miRNA-30e-3p and miRNA-369-3p were involved in the biological processes of protein transport and regulation of cell motion. Conclusion: The target genes SEC22B, RAB10, and FLT1 may be potential biomarkers of AD.
机译:背景:本研究旨在探讨阿尔茨海默氏病(AD)的生物标志物。方法:GSE16759的微阵列数据来自AD患者的4个顶叶组织和年龄匹配的对照参与者的4个顶叶组织的表达谱样本。差异表达的微RNA(miRNA)和基因(DEG)经过分级聚类和功能分析,然后进行目标基因预测。最后,将DEGs定位到靶基因上以构建miRNA调控的网络。结果:共获得427个DEG,并将其分为5个功能。将DEGs定位到预测的目标基因后,建立了313个调节对。靶基因SEC22囊泡运输蛋白同源物B(SEC22B)和SEC63同源物(SEC63)受miRNA-206,RAB10,miRNA-655调控的RAS癌基因家族成员(RAB10)和fms相关酪氨酸激酶1(FLT1)调控miRNA-30e-3p和miRNA-369-3p的作用与蛋白质转运和细胞运动调节的生物学过程有关。结论:目标基因SEC22B,RAB10和FLT1可能是AD的潜在生物标志物。

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