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成人斯蒂尔病患者循环 microRNA-134 的上调及其作为潜在生物标志物的应用。

Upregulation of circulating microRNA-134 in adult-onset Still's disease and its use as potential biomarker.

机构信息

Department of Medical Research, Taichung Veterans General Hospital, Taichung, Taiwan.

Ph.D. Program in Translational Medicine and Rong Hsing Research Center for Translational Medicine, National Chung Hsing University, Taichung, Taiwan.

出版信息

Sci Rep. 2017 Jun 23;7(1):4214. doi: 10.1038/s41598-017-04086-w.

DOI:10.1038/s41598-017-04086-w
PMID:28646209
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5482864/
Abstract

Adult-onset Still's disease (AOSD) is a multi-systemic inflammatory disorder of unknown etiology. To date, no single diagnostic test is available for AOSD. Herein, we investigated the pathogenic role of microRNAs in AOSD. MicroRNA profiles in plasma from AOSD patients and healthy controls were analyzed by microarray analysis, followed by quantitative reverse transcription PCR validation. The biological functions of microRNAs were evaluated using in vitro cell-based assay. Among the differentially expressed microRNAs, microRNA-134 (miR-134) expression was positively correlated with AOSD activity scores and significantly decreased after effective treatment. An increased miR-134 level is significantly associated with the activation of Toll-like receptor 3 (TLR3). The reporter assay identified IL-18 binding protein (IL-18BP) as the target of miR-134. A negative correlation between miR-134 expression and IL-18BP mRNA levels were detected in peripheral blood cells following TLR3 ligand treatment. Lower plasma IL-18BP levels and higher IL-18 levels were also observed in active AOSD patients who had higher miR-134 expression than inactive patients. Upregulation of circulating miR-134 was associated with elevated IL-18 levels by targeting IL-18BP in AOSD patients and was positively correlated with disease activity, suggesting its involvement in AOSD pathogenesis. MiR-134 may be a novel activity indicator or potential prognostic biomarker in AOSD.

摘要

成人斯蒂尔病(AOSD)是一种病因不明的多系统炎症性疾病。迄今为止,尚无针对 AOSD 的单一诊断测试。在此,我们研究了 microRNAs 在 AOSD 中的致病作用。通过微阵列分析分析 AOSD 患者和健康对照者血浆中的 microRNA 谱,然后通过定量逆转录 PCR 验证。使用体外基于细胞的测定来评估 microRNAs 的生物学功能。在差异表达的 microRNAs 中,microRNA-134(miR-134)表达与 AOSD 活性评分呈正相关,并且在有效治疗后显著降低。miR-134 水平的增加与 Toll 样受体 3(TLR3)的激活显著相关。报告基因测定将白细胞介素 18 结合蛋白(IL-18BP)鉴定为 miR-134 的靶标。在 TLR3 配体处理后,在外周血细胞中检测到 miR-134 表达与 IL-18BP mRNA 水平之间存在负相关。在活性 AOSD 患者中也观察到较低的血浆 IL-18BP 水平和较高的 IL-18 水平,这些患者的 miR-134 表达高于非活性患者。在 AOSD 患者中,循环 miR-134 的上调通过靶向 IL-18BP 与升高的 IL-18 水平相关,并且与疾病活性呈正相关,表明其参与 AOSD 的发病机制。miR-134 可能是 AOSD 中的新型活性指标或潜在的预后生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10dd/5482864/5af0b9971916/41598_2017_4086_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10dd/5482864/950a46ad1cce/41598_2017_4086_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10dd/5482864/2ed29b24f246/41598_2017_4086_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10dd/5482864/cc7f17105763/41598_2017_4086_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10dd/5482864/5af0b9971916/41598_2017_4086_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10dd/5482864/950a46ad1cce/41598_2017_4086_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10dd/5482864/2ed29b24f246/41598_2017_4086_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10dd/5482864/cc7f17105763/41598_2017_4086_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10dd/5482864/5af0b9971916/41598_2017_4086_Fig4_HTML.jpg

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