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首页> 外文期刊>Journal of nephrology. >Identification of candidate microRNA biomarkers in diabetic nephropathy: a meta-analysis of profiling studies
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Identification of candidate microRNA biomarkers in diabetic nephropathy: a meta-analysis of profiling studies

机译:患有糖尿病肾病的候选MicroRNA生物标志物的鉴定:剖析谱研究的荟萃分析

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AimsThe aim was to perform a meta-analysis on the miRNA expression profiling studies in diabetic nephropathy (DN) to identify candidate diagnostic biomarkers.MethodsA comprehensive literature search was done in several databases and 53 DN miRNA expression studies were selected. To identify significant DN-miR meta-signatures, two meta-analysis methods were employed: vote-counting strategy and the robust rank aggregation method. The targets of DN-miRs were obtained and a gene set enrichment analysis was carried out to identify the pathways most strongly affected by dysregulation of these miRNAs.ResultsWe identified a significant miRNA meta-signature common to both meta-analysis approaches of three up-regulated (miR-21-5p, miR-146a-5p, miR-10a-5p) and two down-regulated (miR-25-3p and miR-26a-5p) miRNAs. Besides that, subgroup analyses divided and compared the differentially expressed miRNAs according to species (human and animal), types of diabetes (T1DN and T2DN) and tissue types (kidney, blood and urine). Enrichment analysis confirmed that DN-miRs supportively target functionally related genes in signaling and community pathways in DN.ConclusionFive highly significant and consistently dysregulated miRNAs were identified, and future studies should focus on discovering their potential effect on DN and their clinical value as DN biomarkers and therapeutic mediators.
机译:AIMSTHE AIM是对糖尿病肾病(DN)的miRNA表达分析研究进行META分析,以识别候选诊断生物标志物。在几个数据库中完成了综合文学搜索,并选择了53例MIRNA表达研究。为了识别重要的DN-MIR元签名,采用了两种META分析方法:投票计数策略和强大的级别聚集方法。获得DN-MIR的靶标,进行了基因设定的富集分析,以鉴定这些miRNA的失衡最强烈影响的途径。培训术语鉴定了三个上调的荟萃分析方法的显着miRNA元签名(miR-21-5p,miR-146a-5p,miR-10a-5p)和两个下调(miR-25-3p和miR-26a-5p)miRNA。此外,根据物种(人和动物),糖尿病(T1DN和T2DN)和组织类型(肾,血液和尿液),亚组分析除以差异表达的miRNA。富集分析证实,DN-MIRs在DN中的信号传导和社区途径中妥善针对功能相关的基因。确定了高度显着和始终如一的失调的miRNA,未来的研究应专注于发现其对DN的潜在影响及其作为DN生物标志物的临床价值和临床价值。治疗介质。

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