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The Expression of miRNA-146a in Peripheral Blood Mononuclear Cells of Patients with Myasthenia Gravis and Its Bioinformatics Analysis

机译:MiRNA-146A在肌肌肌无力患者外周血单核细胞中的表达及其生物信息学分析

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摘要

The study is to investigate the expression of miRNA-146a in PBMC of myasthenia Gravis (MG), and to explore the molecular regulatory network of miRNA-146a in the pathogenesis of MG by bioinformatics. 108 patients with MG were selected as the experimental group (MG group), and 50 healthy subjects were selected as the control group. The relative expression of miRNA-146a in PBMC was detected by RT-PCR. The cross-target gene of miRNA-146a was predicted by TargetScan and CoMeTa database. miRNA-146a target gene GO enrichment and KEGG Pathway enrichment analysis was performed using the DAVID database. Our results shows that the expression level of miRNA-146a in peripheral blood of MG patients was significantly higher than that of the control group, the difference was statistically significant (P < 0.05), and the nucleotide sequence was highly conserved. The potential target genes of miRNA-146a include 88 kinds; GO analysis showed that miRNA-146a target gene function is mainly enriched in cell proliferation regulation, neuronal differentiation, etc. KEGG Pathway analysis shows that miRNA-146a is mainly enriched in Toll-like receptor signaling pathway, neurotransmitter regulatory signaling pathways, EB signaling pathways and other signaling pathways. In conclusion, the expression of miRNA-146a in PBMC of MG patients is up-regulated and participates in the pathogenesis of MG by acting on multiple signaling pathways.
机译:该研究是探讨MiRNA-146A在肌肌肌肌肌肌肌炎(MG)中的表达,并探讨通过生物信息学的MG发病机制中miRNA-146a的分子调节网络。 108例Mg患者被选为实验组(Mg组),选择50个健康受试者作为对照组。通过RT-PCR检测miRNA-146a在PBMC中的相对表达。 MiRNA-146a的交叉靶基因被TargetScan和Cometa数据库预测。使用David数据库进行MiRNA-146A靶基因致富集和Kegg途径浓缩分析。我们的研究结果表明,MG患者外周血中miRNA-146a的表达水平明显高于对照组,差异有统计学意义(P <0.05),核苷酸序列高度保守。 miRNA-146a的潜在靶基因包括88种; GO分析表明,MiRNA-146A靶基因函数主要富集细胞增殖调节,神经元分化等。Kegg途径分析表明,MiRNA-146a主要富集在收费的受体信号通路,神经递质调节信号通路,EB信号传导途径,EB信号传导途径。和其他信令途径。总之,Mg患者PBMC中miRNA-146a的表达被上调,并通过作用于多信号传导途径参与MG的发病机制。

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