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Circular RNA expression profile in peripheral blood mononuclear cells from Crohn disease patients

机译:克罗恩病患者外周血单个核细胞中环状RNA表达谱

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Crohn disease (CD) is a multifactorial autoimmune disease which is characterized by chronic and recurrent gastrointestinal tract inflammatory disorder. However, the molecular mechanisms of CD remain unclear. Increasing evidences have demonstrated that circular RNAs (circRNAs) participate in the pathogenesis of a variety of disease and were considered as ideal biomarkers in human disease. This study aimed to investigate circRNA expression profiles and detect new biomarkers in inflammatory bowel disease (IBD). Differentially expression of circRNAs between CD and HCs (health controls) were screened by microarray analysis . Peripheral blood mononuclear cells (PBMCs) from 5 CD patients and 5 HCs were included in the microarray analysis . Then, the differences were validated by quantitative polymerase chain reaction (qPCR) following reverse transcription polymerase chain reaction (RT-PCR) in the patients of CD and sex- and age-matched HCs. The most differential expressed circRNA was further validated in ulcerative colitis (UC) patients. Statistical significance between CD, UC, and HCs was analyzed by Student t test for unpaired samples or one-way analysis of variance (ANOVA). Diagnostic value of each circRNA was assessed by receiver operating characteristic (ROC) curve. We identified 155 up-regulated circRNAs and 229 down-regulated ones by microarray analysis in PBMCs from CD patients compared with HCs. Besides, 4 circRNAs (092520, 102610, 004662, and 103124) were significantly up-regulated validated by RT-PCR and qPCR between CD and HCs. ROC curve analysis suggested important values of circRNAs (092520, 102610, 004662, and 103124) in CD diagnosis, with area under the curve (AUC) as 0.66, 0.78, 0.85, and 0.74, respectively. Then, we further identified that the relative expression levels of circRNA_004662 was upregulated significantly in CD patients compared with UC patients. Herein, the upregulation of the 4 circRNAs (092520, 102610, 004662, or 103124) in PBMCs can be served as potential diagnostic biomarkers of CD, and circRNA_004662 might be a novel candidate for differentiating CD from UC. Moreover, a circRNA–microRNA-mRNA network predicted that circRNA_004662 appeared to be correlated with mammalian target of rapamycin (mTOR) pathway.
机译:克罗恩病(CD)是一种多因素自身免疫性疾病,其特征是慢性和复发性胃肠道炎性疾病。但是,CD的分子机制仍不清楚。越来越多的证据表明,环状RNA(circRNA)参与了多种疾病的发病机制,被认为是人类疾病中的理想生物标记。这项研究旨在调查circRNA表达谱并检测炎性肠病(IBD)中的新生物标志物。通过微阵列分析筛选了CD和HCs之间的circRNA差异表达(健康对照)。微阵列分析包括5位CD患者和5位HCs的外周血单个核细胞(PBMC)。然后,通过CD,性别和年龄匹配的HCs患者的逆转录聚合酶链反应(RT-PCR)之后的定量聚合酶链反应(qPCR)验证了差异。在溃疡性结肠炎(UC)患者中进一步验证了差异最大的circRNA。 CD,UC和HCs之间的统计显着性通过未配对样品的Student t检验或单向方差分析(ANOVA)进行了分析。通过受体工作特征(ROC)曲线评估每种circRNA的诊断价值。通过微阵列分析,我们从CD患者的PBMC与HCs中鉴定出155个上调的circRNA和229个下调的circRNA。此外,通过CD和HC之间的RT-PCR和qPCR验证了4个circRNA(092520、102610、004662和103124)被显着上调。 ROC曲线分析表明circRNA(092520、102610、004662和103124)在CD诊断中具有重要价值,曲线下面积(AUC)分别为0.66、0.78、0.85和0.74。然后,我们进一步确定与UC患者相比,CD患者中circRNA_004662的相对表达水平显着上调。在本文中,PBMC中的4个circRNA(092520、102610、004662或103124)的上调可以作为CD的潜在诊断生物标志物,而circRNA_004662可能是将CD与UC区分的新候选物。此外,circRNA–microRNA-mRNA网络预测circRNA_004662似乎与雷帕霉素(mTOR)途径的哺乳动物靶标相关。

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