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Spectrum construction of differentially expressed circular RNAs in patients with leukoaraiosis and function analysis of differentially expressed genes

    作者

    Mi, T;Luo, CJ;Hu, YW;Qu, CQ;Wang, X;Guo, SG;Du, YF

    作者单位

    [Mi, Te] Jining 1 Peoples Hosp, Dept ICU, Jining 272000, Shandong, Peoples R China.;-;[Luo, Changjiang] Shandong Univ, South Branch, Prov Hosp, Dept Neurol, Jinan 250002, Shandong, Peoples R China.;-;[Hu, Yawei] Jining Med Univ, Affiliated Hosp, Dept Neurosurg, Jining 272029, Shandong, Peoples R China.;-;[Qu, Chuanqiang; Wang, Xiang; Guo, Shougang; Du, Yifeng] Shandong Univ, Prov Hosp, Dept Neurol, 324 Jingwuweiqi Rd, Jinan 250021, Shandong, Peoples R China.

    摘要

    Circular RNAs (circRNAs) are class of endogenous RNAs that have a role in the regulation of gene expression. The present study aimed to investigate the diagnostic value and role of circRNA in the pathogenesis of leukoaraiosis (LA). The present study performed Arraystar Human circRNA Array analysis of 6 samples from LA cases and 6 samples from control cases. Differentially expressed (DE) circRNAs between two samples were identified through fold-change (>1.5-fold) screening. Afterwards, based on DE circRNAs, the gene ontology (GO) analysis of upregulated DE genes identified from DE circRNAs demonstrated that DE genes were primarily associated with cellular metabolic processes, membrane-bound organelles and binding. However, none were enriched in the Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway. Downregulated DE genes were enriched in cellular localization, cytoplasm and kinase binding. For the KEGG pathways, the downregulated DE genes were primarily associated with the insulin signaling pathway. The results of the present study indicated that the DE genes from differently expressed circRNAs may have an important role in the pathogenesis of LA and may be a novel targfet for further research.

    关键词

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基本信息

  • 所属机构:

    归属医师: 杜怡峰 郭守刚 王翔 屈传强

    PMID:28677780

    UT:000407461600027

    刊名:MOLECULAR MEDICINE REPORTS

    年,卷(期):2017年16卷3期

    页码:2563-2569

    DOI:10.3892/mmr.2017.6871

    附件: pdf

    收录:   SCIE