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对包括下一代测序技术在内的多发性硬化症中 microRNA 谱的综合分析。

Comprehensive analysis of microRNA profiles in multiple sclerosis including next-generation sequencing.

机构信息

Department of Human Genetics, Saarland University, Germany.

出版信息

Mult Scler. 2014 Mar;20(3):295-303. doi: 10.1177/1352458513496343. Epub 2013 Jul 8.

Abstract

BACKGROUND

MicroRNAs (miRNAs) are short, noncoding RNAs with gene regulatory functions whose expression profiles may serve as disease biomarkers.

OBJECTIVE

The objective of this study was to perform a comprehensive analysis of miRNA expression profiles in blood of patients with a clinically isolated syndrome (CIS) or relapsing-remitting multiple sclerosis (RRMS) including next-generation sequencing (NGS).

METHODS

miRNA expression was analyzed in whole blood samples from treatment-naïve patients with CIS (n = 25) or RRMS (n = 25) and 50 healthy controls by NGS, microarray analysis, and quantitative real-time polymerase chain reaction (qRT-PCR).

RESULTS

In patients with CIS/RRMS, NGS and microarray analysis identified 38 and eight significantly deregulated miRNAs, respectively. Three of these miRNAs were found to be significantly up- (hsa-miR-16-2-3p) or downregulated (hsa-miR-20a-5p, hsa-miR-7-1-3p) by both methods. Another five of the miRNAs significantly deregulated in the NGS screen showed the same direction of regulation in the microarray analysis. qRT-PCR confirmed the direction of regulation for all eight and was significant for three miRNAs.

CONCLUSIONS

This study identifies a set of miRNAs deregulated in CIS/RRMS and reconfirms the previously reported underexpression of hsa-miR-20a-5p in MS. hsa-miR-20a-5p and the other validated miRNAs may represent promising candidates for future evaluation as biomarkers for MS and could be of relevance in the pathophysiology of this disease.

摘要

背景

MicroRNAs (miRNAs) 是具有基因调控功能的短非编码 RNA,其表达谱可能作为疾病的生物标志物。

目的

本研究旨在通过下一代测序 (NGS) 对临床孤立综合征 (CIS) 或复发缓解型多发性硬化症 (RRMS) 患者的血液中的 miRNA 表达谱进行全面分析。

方法

通过 NGS、微阵列分析和定量实时聚合酶链反应 (qRT-PCR) 分析了未经治疗的 CIS(n=25)或 RRMS(n=25)患者和 50 名健康对照者全血样本中的 miRNA 表达。

结果

在 CIS/RRMS 患者中,NGS 和微阵列分析分别鉴定出 38 个和 8 个显著失调的 miRNA。其中 3 个 miRNA 被两种方法发现均显著上调(hsa-miR-16-2-3p)或下调(hsa-miR-20a-5p、hsa-miR-7-1-3p)。在 NGS 筛选中显著失调的另外 5 个 miRNA 在微阵列分析中也表现出相同的调控方向。qRT-PCR 证实了所有 8 个 miRNA 的调控方向,其中 3 个 miRNA 的结果具有统计学意义。

结论

本研究鉴定了一组在 CIS/RRMS 中失调的 miRNAs,并再次证实了 hsa-miR-20a-5p 在 MS 中表达下调的先前报道。hsa-miR-20a-5p 和其他验证的 miRNA 可能是作为 MS 生物标志物的有前途的候选者,并且在该疾病的病理生理学中可能具有相关性。

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