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Analysis of serum microRNA expression in male workers with occupational noise-induced hearing loss

机译:职业噪声引起的听力损失男性工人血清microRNA表达的分析

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摘要

Occupational noise-induced hearing loss (ONIHL) is a prevalent occupational disorder that impairs auditory function in workers exposed to prolonged noise. However, serum microRNA expression in ONIHL subjects has not yet been studied. We aimed to compare the serum microRNA expression profiles in male workers of ONIHL subjects and controls. MicroRNA microarray analysis revealed that four serum microRNAs were differentially expressed between controls (n=3) and ONIHL subjects (n=3). Among these microRNAs, three were upregulated (hsa-miR-3162-5p, hsa-miR-4484, hsa-miR-1229-5p) and one was downregulated (hsa-miR-4652-3p) in the ONIHL group (fold change >1.5 and Pbon value <0.05). Real time quantitative PCR was conducted for validation of the microRNA expression. Significantly increased serum levels of miR-1229-5p were found in ONIHL subjects compared to controls (n=10 for each group; P<0.05). A total of 659 (27.0%) genes were predicted as the target genes of miR-1229-5p. These genes were involved in various pathways, such as mitogen-activated protein kinase (MAPK) signaling pathway. Overexpression of miR-1229-5p dramatically inhibited the luciferase activity of 3′ UTR segment of MAPK1 (P<0.01). Compared to the negative control, HEK293T cells expressing miR-1229-5p mimics showed a significant decline in mRNA levels of MAPK1 (P<0.05). This preliminary study indicated that serum miR-1229-5p was significantly elevated in ONIHL subjects. Increased miR-1229-5p may participate in the pathogenesis of ONIHL through repressing MAPK1 signaling.
机译:职业噪声诱发的听力损失(ONIHL)是一种普遍的职业病,会损害长时间噪声的工人的听觉功能。但是,尚未研究ONIHL受试者的血清microRNA表达。我们的目的是比较ONIHL受试者和对照组中男性工人的血清microRNA表达谱。 MicroRNA微阵列分析显示,四个血清microRNA在对照(n = 3)和ONIHL受试者(n = 3)之间差异表达。在这些microRNA中,ONIHL组中有3个上调的基因(hsa-miR-3162-5p,hsa-miR-4484,hsa-miR-1229-5p)和一个下调的(hsa-miR-4652-3p)(倍数变化) > 1.5且Pbon值<0.05)。进行实时定量PCR以验证microRNA表达。与对照组相比,ONIHL受试者的miR-1229-5p血清水平显着升高(每组n = 10; P <0.05)。预测共有659个(27.0%)基因作为miR-1229-5p的靶基因。这些基因参与了各种途径,例如有丝分裂原激活的蛋白激酶(MAPK)信号传导途径。 miR-1229-5p的过表达显着抑制MAPK1 3'UTR区段的荧光素酶活性(P <0.01)。与阴性对照相比,表达miR-1229-5p模拟物的HEK293T细胞的MAPK1 mRNA水平显着下降(P <0.05)。这项初步研究表明,ONIHL受试者的血清miR-1229-5p显着升高。增加的miR-1229-5p可能通过抑制MAPK1信号传导参与ONIHL的发病机制。

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