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Exploring MicroRNA Biomarkers for Parkinson's Disease from mRNA Expression Profiles

dc.citation.volume7en_US
dc.citation.woscount0en_US
dc.contributor.authorTaguchi, Y-hen_US
dc.contributor.authorWang, Hsiuyingen_US
dc.contributor.department統計學研究所zh_TW
dc.contributor.departmentInstitute of Statisticsen_US
dc.date.accessioned2019-04-02T06:01:02Z
dc.date.available2019-04-02T06:01:02Z
dc.date.issued2018-12-01en_US
dc.description.abstractParkinson'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.en_US
dc.identifier.doi10.3390/cells7120245en_US
dc.identifier.issn2073-4409en_US
dc.identifier.journalCELLSen_US
dc.identifier.urihttp://dx.doi.org/10.3390/cells7120245en_US
dc.identifier.urihttps://ir.lib.nycu.edu.tw/handle/11536/148700
dc.identifier.wosnumberWOS:000455320700023en_US
dc.language.isoen_USen_US
dc.subjectbiomarkeren_US
dc.subjectgeneen_US
dc.subjectmicroRNAen_US
dc.subjectparkinson's diseaseen_US
dc.titleExploring MicroRNA Biomarkers for Parkinson's Disease from mRNA Expression Profilesen_US
dc.typeArticleen_US

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