Hub microRNAs and genes in the development of atrial fibrillation identified by weighted gene co-expression network analysis

被引:0
作者
Qiang Qu
Jin-Yu Sun
Zhen-Ye Zhang
Yue Su
Shan-Shan Li
Feng Li
Ru-Xing Wang
机构
[1] The Affiliated Wuxi People’s Hospital of Nanjing Medical University,Department of Cardiology
[2] The First Affiliated Hospital of Nanjing Medical University,Department of Cardiology
来源
BMC Medical Genomics | / 14卷
关键词
Atrial fibrillation; Weighted gene co-expression network analysis; Hub microRNAs; Hub genes; Inflammation;
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摘要
Co-expression network may contribute to better understanding molecular interaction patterns underlying cellular processes. To explore microRNAs (miRNAs) expression patterns correlated with AF, we performed weighted gene co-expression network analysis (WGCNA) based on the dataset GSE28954. Thereafter, we predicted target genes using experimentally verified databases (ENOCRI, miRTarBase, and Tarbase), and overlapped genes with differentially expressed genes (DEGs) from GSE79768 were identified as key genes. Integrated analysis of association between hub miRNAs and key genes was conducted to screen hub genes. In general, we identified 3 differentially expressed miRNAs (DEMs) and 320 DEGs, predominantly enriched in inflammation-related functional items. Two significant modules (red and blue) and hub miRNAs (hsa-miR-146b-5p and hsa-miR-378a-5p), which highly correlated with AF-related phenotype, were detected by WGCNA. By overlapping the DEGs and predicted target genes, 38 genes were screened out. Finally, 9 genes (i.e. ATP13A3, BMP2, CXCL1, GABPA, LIF, MAP3K8, NPY1R, S100A12, SLC16A2) located at the core region in the miRNA-gene interaction network were identified as hub genes. In conclusion, our study identified 2 hub miRNAs and 9 hub genes, which may improve the understanding of molecular mechanisms and help to reveal potential therapeutic targets against AF.
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