Lu Yingjie, Meng Xiangwei, Wang Lifeng, Wang Xiaoyun
Department of Cardiology, The Fourth Clinical Hospital of Harbin Medical University, Harbin, Heilongjiang 150001, P.R. China.
Department of Radiology, The Fourth Clinical Hospital of Harbin Medical University, Harbin, Heilongjiang 150001, P.R. China.
Exp Ther Med. 2018 Feb;15(2):1376-1384. doi: 10.3892/etm.2017.5573. Epub 2017 Nov 27.
It has been demonstrated that long non-coding RNAs (lncRNAs) are important in the gene regulatory network and their dysregulated expression has been implicated in cardiovascular disease. However, little is known regarding lncRNA expression patterns and their function in the progression of acute coronary syndromes (ACSs). In the present study, the expression profiles of lncRNAs from 52 patients with ACS were analyzed by re-annotating existing microarray data. The lncRNA expression profiles in the two distinct clinical entities of ACS, myocardial infarction (MI) and unstable angina (UA), were examined. Out of the 2,332 lncRNAs assessed, it was identified that 18 lncRNAs were upregulated and 35 lncRNAs were downregulated in patients with MI compared to those with UA. Furthermore, the expression profiles of patients with ACS were compared at different time points and significantly altered lncRNA expression was observed during the progression of ACS. A total of 7 candidate lncRNA biomarkers were identified and an lncRNA-based classifier was developed to predict MI risk based on the expression data of the 7 lncRNAs using random forest and support vector machine strategies. This achieved a classification accuracy of 90.38% with a sensitivity of 100% and a specificity of 68.75%. Additionally, functional analysis suggested that these 7 lncRNAs may be involved in known MI-associated biological processes and pathways.
已有研究表明,长链非编码RNA(lncRNA)在基因调控网络中具有重要作用,其表达失调与心血管疾病有关。然而,关于lncRNA在急性冠状动脉综合征(ACS)进展中的表达模式及其功能,我们知之甚少。在本研究中,通过重新注释现有的微阵列数据,分析了52例ACS患者lncRNA的表达谱。研究了ACS的两种不同临床类型,即心肌梗死(MI)和不稳定型心绞痛(UA)中的lncRNA表达谱。在评估的2332个lncRNA中,发现与UA患者相比,MI患者中有18个lncRNA上调,35个lncRNA下调。此外,对ACS患者在不同时间点的表达谱进行了比较,发现在ACS进展过程中lncRNA表达发生了显著变化。共鉴定出7个候选lncRNA生物标志物,并开发了一种基于lncRNA的分类器,使用随机森林和支持向量机策略,根据这7个lncRNA的表达数据预测MI风险。其分类准确率达到90.38%,敏感性为100%,特异性为68.75%。此外,功能分析表明,这7个lncRNA可能参与已知的与MI相关的生物学过程和通路。