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  • ISSN 1674-8301
  • CN 32-1810/R
Volume 35 Issue 6
Nov.  2021
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Kai Wang, Zhongming Li, Wenjie Ma, Yan Sun, Xianling Liu, Lijun Qian, Jian Hong, Dasheng Lu, Jing Zhang, Di Xu. Construction of miRNA-mRNA network reveals crucial miRNAs and genes in acute myocardial infarction[J]. The Journal of Biomedical Research, 2021, 35(6): 425-435. DOI: 10.7555/JBR.35.20210088
Citation: Kai Wang, Zhongming Li, Wenjie Ma, Yan Sun, Xianling Liu, Lijun Qian, Jian Hong, Dasheng Lu, Jing Zhang, Di Xu. Construction of miRNA-mRNA network reveals crucial miRNAs and genes in acute myocardial infarction[J]. The Journal of Biomedical Research, 2021, 35(6): 425-435. DOI: 10.7555/JBR.35.20210088
shu

Construction of miRNA-mRNA network reveals crucial miRNAs and genes in acute myocardial infarction

  • 1.

    Department of Cardiology

  • 2.

    Department of Geriatrics, the First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu 210029, China

  • 3.

    Department of Cardiology, the Second Affiliated Hospital of Wannan Medical College, Wuhu, Anhui 241000, China

More Information
  • Corresponding author:

    Di Xu, Department of Geriatrics, the First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, Nanjing, Jiangsu 210029, China. Tel: +86-25-68305071, E-mail: xudi@jsph.org.cn; Jing Zhang, Department of Cardiology, the First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, Nanjing, Jiangsu 210029, China. Tel: +86-25-68303131, E-mail: zj_njmu@163.com

  • Received Date: June 02, 2021
  • Revised Date: August 01, 2021
  • Accepted Date: August 05, 2021
  • Available Online: October 09, 2021
    Graphical Abstract
    • Abstract
  • Acute myocardial infarction (AMI) is a severe cardiovascular disease. This study aimed to identify crucial microRNAs (miRNAs) and mRNAs in AMI by establishing a miRNA-mRNA network. The microarray datasets GSE31568, GSE148153, and GSE66360 were downloaded from the Gene Expression Omnibus (GEO) database. We identified differentially expressed miRNAs (DE-miRNAs) and mRNAs (DE-mRNAs) in AMI samples compared with normal control samples. The consistently changing miRNAs in both GSE31568 and GSE148153 datasets were selected as candidate DE-miRNAs. The interactions between the candidate DE-miRNAs and DE-mRNAs were analyzed, and a miRNA-mRNA network and a protein-protein interaction network were constructed, along with functional enrichment and pathway analyses. A total of 209 DE-miRNAs in the GSE31568 dataset, 857 DE-miRNAs in the GSE148153 dataset, and 351 DE-mRNAs in the GSE66360 dataset were identified. Eighteen candidate DE-miRNAs were selected from both the GSE31568 and GSE148153 datasets. Furthermore, miR-646, miR-127-5p, miR-509-5p, miR-509-3-5p, and miR-767-5p were shown to have a higher degree in the miRNA-mRNA network. THBS-1 as well as FOS was a hub gene in the miRNA-mRNA network and the protein-protein interaction (PPI) network, respectively. CDKN1A was important in both miRNA-mRNA network and PPI network. We established a miRNA-mRNA network in AMI and identified five miRNAs and three genes, which might be used as biomarkers and potential therapeutic targets for patients with AMI.
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