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通过靶向NF-кb/TNF-α途径中的TNFSF4和SP1研究miR-106a、miR-125b和miR-330与多发性硬化症患者的相关性:一项病例对照研究

Study of The Correlation between miR-106a, miR-125b, and miR-330 on Multiple Sclerosis Patients by Targeting TNFSF4 and SP1 in NF-кb/TNF-α Pathway: A Case-Control Study.

作者信息

Hadi Nasrin, Seifati Seyed Morteza, Nateghi Behnaz, Ravaghi Parisa, Khosravian Farinaz, Namazi Faezeh, Fotouhi Firouzabad Maryam, Shaygannejad Vahid, Salehi Mansoor

机构信息

Medical Biotechnology Research Center, Ashkezar Branch, Islamic Azad University, Ashkezar, Yazd, Iran.

Medical Genetics Research Center of Genome, Isfahan University of Medical Sciences, Isfahan, Iran.

出版信息

Cell J. 2022 Jul 27;24(7):403-409. doi: 10.22074/cellj.2022.7835.

Abstract

OBJECTIVE

Multiple sclerosis (MS) is a complex multifactorial neuro-inflammatory disorder. This complexity arises from the evidence suggesting that MS is developed by interacting with environmental and genetic factors. This study aimed to evaluate the miR-106a, miR-125b, and miR330- expression levels in relapsing-remitting multiple sclerosis (RRMS) patients. The miRNAs' impact on TNFSF4 and Sp1 genes through the NF-кB/TNF-α signaling pathway was analyzed by measuring the expression levels in case and controls.

MATERIALS AND METHODS

In this in silico-experimental study, we evaluated the association of miR-106a, miR- 125b, and miR330- with TNFSF4 and SP1 gene expression levels in 60 RRMS patients and 30 healthy controls by real-time polymerase chain reaction (PCR).

RESULTS

The expression levels of miR-330, miR-106a, and miR125-b in blood samples of RRMS patients were predominantly reduced. The expression of TNFSF4 in patients demonstrated a significant enhancement, in contrast to the diminishing Sp1 gene expression level in controls.

CONCLUSION

Our findings indicated an association between miR-106a and miR-330 and miR125-b expression and RRMS in our study population. Our data suggested that the miR106-a, miR125-b, and mir330- expression are correlated with TNFSF4 and Sp1 gene expression levels.

摘要

目的

多发性硬化症(MS)是一种复杂的多因素神经炎症性疾病。这种复杂性源于有证据表明MS是通过与环境和遗传因素相互作用而发展形成的。本研究旨在评估复发缓解型多发性硬化症(RRMS)患者中miR-106a、miR-125b和miR330的表达水平。通过测量病例组和对照组的表达水平,分析了这些微小RNA通过NF-кB/TNF-α信号通路对TNFSF4和Sp1基因的影响。

材料与方法

在这项计算机模拟实验研究中,我们通过实时聚合酶链反应(PCR)评估了60例RRMS患者和30例健康对照中miR-106a、miR-125b和miR330与TNFSF4和SP1基因表达水平的相关性。

结果

RRMS患者血样中miR-330、miR-106a和miR125-b的表达水平大多降低。患者中TNFSF4的表达显著增强,而对照组中Sp1基因表达水平则降低。

结论

我们的研究结果表明,在我们的研究人群中,miR-106a、miR-330和miR125-b的表达与RRMS之间存在关联。我们的数据表明,miR106-a、miR125-b和mir330的表达与TNFSF4和Sp1基因表达水平相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/407e/9428476/3d3a422e031d/Cell-J-24-403-g01.jpg

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