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

被引:7
|
作者
Qu, Qiang [1 ,2 ]
Sun, Jin-Yu [1 ,2 ]
Zhang, Zhen-Ye [1 ]
Su, Yue [1 ,2 ]
Li, Shan-Shan [1 ]
Li, Feng [1 ]
Wang, Ru-Xing [1 ]
机构
[1] Nanjing Med Univ, Dept Cardiol, Affiliated Wuxi Peoples Hosp, 299 Qingyang Rd, Wuxi 214023, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Dept Cardiol, Affiliated Hosp 1, Nanjing 210029, Peoples R China
基金
中国国家自然科学基金;
关键词
Atrial fibrillation; Weighted gene co-expression network analysis; Hub microRNAs; Hub genes; Inflammation; EXPRESSION PROFILES; CLIP-SEQ; INFLAMMATION; MIRNA; ACTIVATION; PROTEINS; STARBASE; MODULES; TOOL;
D O I
10.1186/s12920-021-01124-5
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
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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页数:12
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