hsa-miR-520d-3p and hsa-miR-449a are Candidate MicroRNA Regulators in Multiple Sclerosis.

IF 1.5 Q2 MEDICINE, GENERAL & INTERNAL
Nafiseh Karimi, Majid Motovali Bashi, Mostafa Ghaderi-Zefrehei, Bluma J Lesch
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引用次数: 0

Abstract

Background: An incapacitating chronic inflammatory neurodegenerative illness, known as multiple sclerosis (MS), is characterized by lymphocyte infiltration into the central nervous system. We aimed to identify specific miRNAs whose altered expression correlates with MS diagnosis and therapy selection, which could be biomarkers for these aspects of the disease.

Methods: The GSE21079 dataset was obtained for this study using Geoquery version 2.50.5 from the Gene Expression Omnibus database. The miRNAs exhibiting the highest variance were selected, and a miRNA-miRNA interaction network was constructed through a Bayesian network utilizing the bnlearn R package (version 4.7.1). The adjacency matrix generated from the learned network was subsequently analyzed in the Cytoscape environment. For the workbench lab, whole blood samples were collected from the MS Research Center and Al-Zahra Hospital in Isfahan, Iran, between June 2019 and October 2019. RNA extraction was conducted in the laboratory at Isfahan University. Real-time PCR (RT-PCR) was employed to validate the expression changes of the candidate mirRNAs (hsa-miR-520d-3p, hsa-miR-449a). The results were analyzed using REST 2009 software.

Results: The Notch1 signaling pathway was targeted by hsa-miR-520d-3p and hsa-miR-449a in MS patients, which led to downregulation of critical genes, such as LIM and SH3 protein 1 (LASP1), Tubulin Alpha1c (TUBA1C), and S100 calcium binding protein A6 (S100A6). Furthermore, the results from RT-PCR among 50 whole blood samples, comprising 30 cases of MS and 20 control cases, indicated that the expression levels of miRNA in patients with MS exhibited a statistically significant difference compared to those in healthy individuals, with values of 0.324 for hsa-miR-520d-3p and 0.075 for hsa-miR-449a. These values correspond to a downregulation of 3.1-fold and 13.3-fold, respectively.

Conclusion: The findings indicate that MS patients have lower expression levels of hsa-miR-520d-3p and hsa-miR-449a.

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hsa-miR-520d-3p和hsa-miR-449a是多发性硬化症的候选MicroRNA调节因子。
背景:多发性硬化症(MS)是一种慢性炎症性神经退行性疾病,以淋巴细胞浸润中枢神经系统为特征。我们的目的是鉴定特异性mirna,其表达改变与MS诊断和治疗选择相关,这可能是该疾病这些方面的生物标志物。方法:使用Gene Expression Omnibus数据库中的Geoquery version 2.50.5获取GSE21079数据集。选择方差最大的mirna,利用bnlearn R软件包(版本4.7.1)通过贝叶斯网络构建miRNA-miRNA相互作用网络。随后在Cytoscape环境中分析由学习到的网络生成的邻接矩阵。工作台实验室在2019年6月至2019年10月期间从伊朗伊斯法罕的MS研究中心和Al-Zahra医院收集了全血样本。RNA提取在伊斯法罕大学的实验室进行。采用Real-time PCR (RT-PCR)验证候选mirRNAs (hsa-miR-520d-3p, hsa-miR-449a)的表达变化。使用REST 2009软件对结果进行分析。结果:MS患者Notch1信号通路被hsa-miR-520d-3p和hsa-miR-449a靶向,导致LIM和SH3蛋白1 (LASP1)、微管蛋白Alpha1c (TUBA1C)、S100钙结合蛋白A6 (S100A6)等关键基因下调。此外,对30例MS患者和20例对照患者的50份全血样本进行RT-PCR分析结果显示,MS患者的miRNA表达水平与健康人群相比,差异有统计学意义,hsa-miR-520d-3p的表达值为0.324,hsa-miR-449a的表达值为0.075。这些值分别对应于下调3.1倍和13.3倍。结论:研究结果提示MS患者hsa-miR-520d-3p和hsa-miR-449a表达水平较低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Iranian Journal of Medical Sciences
Iranian Journal of Medical Sciences MEDICINE, GENERAL & INTERNAL-
CiteScore
3.20
自引率
0.00%
发文量
84
审稿时长
12 weeks
期刊介绍: The Iranian Journal of Medical Sciences (IJMS) is an international quarterly biomedical publication, which is sponsored by Shiraz University of Medical Sciences. The IJMS intends to provide a scientific medium of com­muni­cation for researchers throughout the globe. The journal welcomes original clinical articles as well as clinically oriented basic science re­search experiences on prevalent diseases in the region and analysis of various regional problems.
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