Taguchi Y-H, Wang Hsiuying
Department of Physics, Chuo University, 1-13-27 Kasuga, Bunky-ku, Tokyo 112-8551, Japan.
Institute of Statistics, National Chiao Tung University, Hsinchu 30010, Taiwan.
Cells. 2018 Dec 5;7(12):245. doi: 10.3390/cells7120245.
Parkinson's disease (PD) is a chronic, progressive neurodegenerative disease characterized by both motor and nonmotor features. The diagnose of PD is based on a review of patients' signs and symptoms, and neurological and physical examinations. So far, no tests have been devised that can conclusively diagnose PD. In this study, we explore both microRNA and gene biomarkers for PD. Microarray gene expression profiles for PD patients and healthy control are analyzed using a principal component analysis (PCA)-based unsupervised feature extraction (FE). 244 genes are selected to be potential gene biomarkers for PD. In addition, we implement these genes into Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways, and find that the 15 microRNAs (miRNAs), hsa-miR-92a-3p, 16-5p, 615-3p, 877-3p, 100-5p, 320a, 877-5p, 23a-3p, 484, 23b-3p, 15a-5p, 324-3p, 19b-3p, 7b-5p and 505-3p, significantly target these 244 genes. These miRNAs are shown to be significantly related to PD. This reveals that both selected genes and miRNAs are potential biomarkers for PD.
帕金森病(PD)是一种慢性进行性神经退行性疾病,具有运动和非运动特征。PD的诊断基于对患者体征和症状的评估以及神经学和体格检查。到目前为止,尚未设计出能够确诊PD的检测方法。在本研究中,我们探索了PD的微小RNA和基因生物标志物。使用基于主成分分析(PCA)的无监督特征提取(FE)分析PD患者和健康对照的微阵列基因表达谱。选择244个基因作为PD的潜在基因生物标志物。此外,我们将这些基因应用于京都基因与基因组百科全书(KEGG)通路,发现15种微小RNA(miRNA),即hsa-miR-92a-3p、16-5p、615-3p、877-3p、100-5p、320a、877-5p、23a-3p、484、23b-3p、15a-5p、324-3p、19b-3p、7b-5p和505-3p,显著靶向这些244个基因。这些miRNA显示与PD显著相关。这表明所选的基因和miRNA都是PD的潜在生物标志物。