多发性硬化症患者p50相关COX-2外基因RNA和NF-Kappa B相互作用长链非编码RNA的表达分析

Zeinab Shirvani-Farsani , Mina Rezaei , Zahra Abedi Kichi , Mehrdad Behmanesh , Shirin Farivar
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引用次数: 0

摘要

炎性长链非编码RNA (lncRNAs)包括PACER (p50相关的COX-2外基因RNA)和NKILA (NF-Kappa B相互作用的长链非编码RNA),最近在多发性硬化症(MS)患者的免疫和炎症途径中成为必不可少的调节因子,可能具有诊断、预后和治疗靶点的价值。在本研究中,我们旨在评估PACER、NKILA lncRNAs、CTCF (ccctc结合因子)和NF-κB在MS患者和对照组外周血单个核细胞中的表达。我们利用实时荧光定量PCR检测了39例MS患者和37例健康对照中PACER、CTCF、NKILA和NF-kB的表达水平。研究结果显示,MS患者中PACER lncRNA和CTCF的表达水平较对照组明显下降,而NKILA lncRNA和NF-κB的表达水平未见明显下降,可能参与了MS的发病机制。值得注意的是,PACER和CTCF的ROC曲线下面积分别高达0.80和0.68。基于这些观察,PACER和CTCF在区分MS患者和健康对照者的疾病状态方面具有最好的效率。CTCF低表达水平与PACER lncRNA、NF-KB表达水平以及病程、年龄、EDSS等因素相关。总之,这些结果表明PACER lncRNA和CTCF可能与MS风险相关。然而,需要进一步的功能研究来确认这些基因在MS病因中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Expression analysis of p50-associated COX-2 extragenic RNA and NF-Kappa B Interacting long non-coding RNA in multiple sclerosis patients

Inflammatory long non-coding RNAs (lncRNAs) including PACER (p50-associated COX-2 extragenic RNA) and NKILA (NF-Kappa B Interacting long non-coding RNA) and have recently emerged as essential regulators in immune and inflammation pathways in patients with multiple sclerosis (MS), which have possible worthiness as diagnostic, prognostic, and therapeutic targets. In the current study, we aimed to evaluate the expressions of PACER, NKILA lncRNAs, CTCF (CCCTC-binding factor), and NF-κB in the PBMC (peripheral blood mononuclear cells) from MS patients and control subjects. We detected the expression levels of PACER, CTCF, NKILA, and NF-kB using real-time PCR in 39 MS patients and 37 healthy controls. The findings show that the expression levels of PACER lncRNA and CTCF, but not NKILA lncRNA and NF-κB, have significantly decreased in MS patients compared to the controls, so they are probably involved in MS pathogenesis. Notably, the area under the ROC curve for PACER and CTCF was up to 0.80 and 0.68, respectively. Based on these observations, the PACER and CTCF had been shown to have the best efficiency in the discrimination of disease status between MS patients and healthy controls. A low expression level of CTCF was correlated with PACER lncRNA and NF-KB expression levels as well as some factors including disease duration, age, and EDSS. Altogether, these results demonstrate that PACER lncRNA and CTCF were potentially related to the MS risk. However, further functional investigations are required to confirm the roles of these genes in the etiology of MS.

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