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微小RNA-584和微小RNA-146是急性呼吸窘迫综合征的候选生物标志物。

miR-584 and miR-146 are candidate biomarkers for acute respiratory distress syndrome.

作者信息

Zhang Siquan, Hong Yinuo, Liu Huafeng, Wang Qianpeng, Xu Juan, Zhang Yujuan, Zhao Xi, Yao Yan, Zhou Kexing, Ding Xianfeng

机构信息

Intensive Care Unit, XiXi Hospital of Hangzhou, Hangzhou, Zhejiang 310023, P.R. China.

College of Life Sciences and Medicine, Zhejiang Sci-Tech University, Hangzhou, Zhejiang 310018, P.R. China.

出版信息

Exp Ther Med. 2021 May;21(5):445. doi: 10.3892/etm.2021.9873. Epub 2021 Mar 1.

Abstract

MicroRNAs (miRNAs/miRs) have important roles in inflammation and infections, which are common manifestations of acute respiratory distress syndrome (ARDS). The present study aimed to assess whether serum miRNAs are potential diagnostic biomarkers for human ARDS. For this, two sets of serum samples from healthy individuals and patients with ARDS were analysed by high-throughput sequencing to identify differentially expressed genes in ARDS. A total of 679 valid sequences were identified as differentially expressed (P<0.05). Of these, five differentially expressed miRNAs were subjected to reverse transcription-quantitative PCR validation. Finally, two miRNAs (miR-584 and miR-146a) were successfully verified. These two miRNAs were significantly downregulated in the serum of patients with ARDS. Gene Ontology annotations and Kyoto Encyclopedia of Genes and Genomes pathway analysis revealed that their target transcripts were implicated in a broad range of biological processes and various metabolic pathways, including involvement in the regulation of various inflammatory factors. The present study provided a framework for understanding the molecular mechanisms of ARDS and suggested that miR-584 and miR-146a are associated with ARDS and may be potential therapeutic targets.

摘要

微小RNA(miRNA/miR)在炎症和感染中发挥着重要作用,而炎症和感染是急性呼吸窘迫综合征(ARDS)的常见表现。本研究旨在评估血清miRNA是否为人类ARDS的潜在诊断生物标志物。为此,通过高通量测序分析了两组来自健康个体和ARDS患者的血清样本,以鉴定ARDS中差异表达的基因。共鉴定出679个有效序列差异表达(P<0.05)。其中,对5个差异表达的miRNA进行了逆转录定量PCR验证。最后,成功验证了两个miRNA(miR-584和miR-146a)。这两个miRNA在ARDS患者血清中显著下调。基因本体注释和京都基因与基因组百科全书通路分析表明,它们的靶转录本涉及广泛的生物学过程和各种代谢途径,包括参与多种炎症因子的调控。本研究为理解ARDS的分子机制提供了一个框架,并表明miR-584和miR-146a与ARDS相关,可能是潜在的治疗靶点。

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