Zhang Huan, Li Tao, Wu Guanji, Ma Feng
Department of Cardiovascular Medicine, Xi'an Central Hospital, Xi'an, Shaanxi 710003, P.R. China.
Exp Ther Med. 2014 May;7(5):1151-1154. doi: 10.3892/etm.2014.1610. Epub 2014 Mar 7.
Coronary artery disease (CAD) is the most common type of cardiovascular disease and leading cause of mortality worldwide. Microarray technology for gene expression analysis has facilitated the identification of the molecular mechanism that underlies the pathogenesis of CAD. Previous studies have primarily used variance or regression analysis, without considering array specific factors. Thus, the aim of the present study was to investigate the mechanism of CAD using partial least squares (PLS)-based analysis, which was integrated with the Monte Carlo technique. Microarray analysis was performed with a data set of 110 CAD patients and 111 controls obtained from the Gene Expression Omnibus database. A total of 390 dysregulated genes were acquired. Significantly increased representations of dysregulated genes in Gene Ontology items, including transforming growth factor β-activated receptor activity and acyl-CoA oxidase activity, were identified. Network analysis revealed three hub genes with a degree of >10, including ESR1, ITGA4 and ARRB2. The results of the present study provide novel information on the gene expression signatures of CAD patients and offer further theoretical support for future therapeutic study.
冠状动脉疾病(CAD)是最常见的心血管疾病类型,也是全球范围内的主要死因。用于基因表达分析的微阵列技术有助于识别CAD发病机制背后的分子机制。先前的研究主要使用方差或回归分析,而未考虑阵列特定因素。因此,本研究的目的是使用基于偏最小二乘法(PLS)并结合蒙特卡罗技术的分析方法来研究CAD的机制。对从基因表达综合数据库获得的110例CAD患者和111例对照的数据集进行了微阵列分析。共获得390个失调基因。在基因本体项目中,包括转化生长因子β激活受体活性和酰基辅酶A氧化酶活性,失调基因的代表性显著增加。网络分析揭示了三个度大于10的枢纽基因,包括ESR1、ITGA4和ARRB2。本研究结果提供了关于CAD患者基因表达特征的新信息,并为未来的治疗研究提供了进一步的理论支持。