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The correlation of long non-coding RNA NEAT1 and its targets microRNA (miR)-21, miR-124, and miR-125a with disease risk, severity, and inflammation of allergic rhinitis

机译:长期非编码RNA Neat1及其靶标microRNA(miR)-21,miR-124和miR-125a具有疾病风险,严重程度和过敏性鼻炎炎症的相关性的相关性

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ABSTRACT:The present study aimed to investigate the correlation of long non-coding RNA nuclear-enriched abundant transcript 1 (lncRNA NEAT1) with microRNA (miR)-21, miR-124, and miR-125a, and their associations with disease risk, severity, and inflammatory cytokines of allergic rhinitis (AR).Totally 70 AR patients and 70 non-atopic obstructive snoring patients (as controls) were recruited. Inferior turbinate mucosa samples were collected from all participants for lncRNA NEAT1, its targets (miR-21, miR-124, and miR-125a), interleukin (IL)-4, IL-6, IL-10, and IL-17 detection via reverse transcription quantitative polymerase chain reaction. Disease severity of AR patients was assessed using individual nasal symptom score (INSS) and total nasal symptom score (TNSS).LncRNA NEAT1 was upregulated, while miR-21, miR-124, and miR-125a were downregulated in AR patients compared with controls. Additionally, lncRNA NEAT1, miR-21, and miR-125a displayed good values in differentiating AR patients from controls, while miR-124 could only slightly differentiate AR patients from controls. In AR patients, lncRNA NEAT1 was negatively associated with miR-21 and miR-125a, but not miR-124. However, in controls, no correlation of lncRNA NEAT1 with miR-21, miR-124, or miR-125a was observed. Furthermore, in AR patients, lncRNA NEAT1 was positively, while miR-21 and miR-125a was negatively associated with INSS (rhinorrhea, itching, congestion scores), TNSS and inflammatory cytokines; however, correlation of miR-124 with INSS, TNSS, and inflammatory cytokines was slight.LncRNA NEAT1 and its targets (miR-21 and miR-125a) present close correlations with disease risk, severity, and inflammation of AR, suggesting their potential as biomarkers for AR assessment.Copyright ? 2021 the Author(s). Published by Wolters Kluwer Health, Inc.
机译:摘要:本研究旨在探讨长期非编码RNA核富含丰富转录物1(LNCRNA Neat1)与MicroRNA(miR)-21,miR-124和miR-125a的相关性,以及它们与疾病风险的关联,严重程度和过敏性鼻炎(AR)的炎症细胞因子。招募了70例患者和70例非特应性阻塞性打鼾患者(作为对照)。从所有参与者的LNCRNA Neat1,其靶标(miR-21,miR-124和miR-125a),白细胞介素(IL)-4,IL-6,IL-10和IL-17检测中收集下鼻甲粘膜样品通过逆转录定量聚合酶链反应。使用单个鼻腔症状评分(INSS)评估AR患者的疾病严重程度,并且鼻腔症状评分(TNSS).LNCRNA neat1被上调,而MIR-21,MIR-124和MIR-125A在AR患者中下调,与对照相比,在AR患者中下调。另外,LNCRNA Neat1,miR-21和miR-125a在区分AR患者免受对照的情况下显示出良好的值,而MIR-124只能略微区分AR患者来自对照的患者。在AR患者中,LNCRNA Neat1与miR-21和miR-125a负相关,但不是miR-124。然而,在对照中,观察到与miR-21,miR-124或miR-125a的LNCRNA Neat1的相关性。此外,在AR患者中,LNCRNA Neat1是正面的,而miR-21和miR-125a与INSS(鼻子,瘙痒,充血分数),TNS和炎症细胞因子负相关;然而,MiR-124与INSS,TNSS和炎性细胞因子的相关性是轻微的.LNACRNA Neat1及其靶标(miR-21和miR-125a)与AR的疾病风险,严重程度和炎症存在密切相关,表明其潜力AR评估的生物标志物。 2021提交人。由Wolters Kluwer Health,Inc。出版

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