Novosadova Eva, Chabronova Alzbeta, Kolek Vitezslav, Petrek Martin, Navratilova Zdenka
Laboratory of Immunogenomics, Department of Pathological Physiology, Faculty of Medicine and Dentistry, Palacky University, Olomouc, Czech Republic.
Department of Respiratory Medicine and TBC, Palacky University, Olomouc, Czech Republic.
Mediators Inflamm. 2016;2016:1246129. doi: 10.1155/2016/1246129. Epub 2016 Dec 5.
. Pulmonary sarcoidosis is associated with dysregulated expression of intracellular miRNAs. There is however only little information on extracellular miRNAs and their association with the disease course in sarcoidosis. We therefore assessed serum miRNAs in sarcoidosis classified according to the presence of Löfgren's syndrome (LS) as a hallmark of good prognosis in contrast to more advanced disease course. . RT-PCR was used to assess 35 miRNAs in 13 healthy controls and 24 sarcoidosis patients (12 with X-ray (CXR) stage ≤ 1 and LS and 12 with insidious onset and CXR stage ≥ 3). . Compared to controls, we consistently observed dysregulated expressions of miR-146, miR-16, miR-425-5p, and miR-93-5p in both sarcoidosis groups irrespective of disease course. Specifically, patients without LS had dysregulated expressions of miR-150-5p, miR-1, and miR-212 compared to controls. Patients with LS had dysregulated expressions of miR-21-5p and miR-340-5p compared to controls. Bioinformatics predicted consistently "Pathways in cancer" to be modulated by both altered profiles in patients with/without LS. Three miRNAs (miR-21-5p, miR-340-5p, and miR-212-3p) differed between our patients with LS and those without LS; their cumulative effect may modulate "TGF- signalling pathway." . Further study should focus on possible applications of serum miRNAs for diagnostics follow-up and for prognosis.
肺结节病与细胞内微小RNA(miRNA)表达失调有关。然而,关于细胞外miRNA及其与结节病病程的关联,目前所知甚少。因此,我们评估了根据 Löfgren 综合征(LS)的存在进行分类的结节病患者血清中的miRNA,LS是预后良好的标志,与病程更进展的情况形成对比。采用逆转录-聚合酶链反应(RT-PCR)评估了13名健康对照者和24名结节病患者(12名X线(CXR)分期≤1且有LS的患者以及12名隐匿起病且CXR分期≥3的患者)中的35种miRNA。与对照组相比,我们在两个结节病组中均持续观察到miR-146、miR-16、miR-425-5p和miR-93-5p的表达失调,无论病程如何。具体而言,与对照组相比,无LS的患者miR-150-5p、miR-1和miR-212表达失调。与对照组相比,有LS的患者miR-21-5p和miR-340-5p表达失调。生物信息学预测“癌症通路”在有/无LS的患者中均受改变谱的调节。我们有LS和无LS的患者之间有三种miRNA(miR-21-5p、miR-340-5p和miR-212-3p)存在差异;它们的累积效应可能调节“转化生长因子(TGF)信号通路”。进一步的研究应聚焦于血清miRNA在诊断随访和预后方面的可能应用。