Mao Zhanglin, Wu Fen, Shan Yunfeng
Department of Vascular Surgery, Yiwu Central Hospital, Yiwu, Zhejing, China, Yiwu Department of Hepatobiliary Surgery, Yiwu Central Hospital, Yiwu, Zhejiang, China.
Medicine (Baltimore). 2018 Mar;97(13):e9832. doi: 10.1097/MD.0000000000009832.
This study was aimed to explore the crucial genes and microRNAs (miRNAs) associated with the carotid atherosclerosis (CA).Two public datasets GSE28829 and GSE43292 were obtained from Gene Expression Omnibus databases to analyze the differentially expressed genes (DEGs) between primary and advanced atherosclerotic plaque tissues. The Gene Ontology (GO) terms, pathways, and protein-protein interactions (PPIs) of these DEGs were analyzed. miRNAs and transcription factor (TF) were predicted.A total of 112 upregulated and 179 downregulated intersection DEGs were identified between 2 datasets. In the PPI network, HSP90AB1 (degree = 19), RAP1A (degree = 14), and integrin subunit beta 1 (ITGB1) had higher degrees. A total of 23 miRNAs were predicted, such as miR-126, miR-155, miR-19A, and miR-19B. Four TFs were associated with upregulated DEGs, while 10 TFs were identified to be associated with downregulated genes.Our study suggests the important roles of HSP90AB1, RAP1A, and integrins proteins of ITGB1, ITGA11, ITGA9, and ITGB2 in the progression of CA plaque. Additionally, miR-126, miR-155, miR-19B, and miR-19A may be considered as biomarkers of CA.
本研究旨在探索与颈动脉粥样硬化(CA)相关的关键基因和微小RNA(miRNA)。从基因表达综合数据库中获取了两个公共数据集GSE28829和GSE43292,以分析原发性和晚期动脉粥样硬化斑块组织之间的差异表达基因(DEG)。对这些DEG的基因本体(GO)术语、信号通路和蛋白质-蛋白质相互作用(PPI)进行了分析。预测了miRNA和转录因子(TF)。在两个数据集中共鉴定出112个上调和179个下调的交集DEG。在PPI网络中,热休克蛋白90α家族类B成员1(HSP90AB1,度 = 19)、Ras相关蛋白1A(RAP1A,度 = 14)和整合素β1亚基(ITGB1)的度较高。共预测了23个miRNA,如miR-126、miR-155、miR-19A和miR-19B。4个TF与上调的DEG相关,而10个TF被确定与下调基因相关。我们的研究表明,HSP90AB1、RAP1A以及ITGB1、ITGA11、ITGA9和ITGB2的整合素蛋白在CA斑块进展中具有重要作用。此外,miR-126、miR-155、miR-19B和miR-19A可被视为CA的生物标志物。