4.6 Article

Potentially Functional microRNA-mRNA Regulatory Networks in Intestinal Ischemia-Reperfusion Injury: A Bioinformatics Analysis

期刊

JOURNAL OF INFLAMMATION RESEARCH
卷 14, 期 -, 页码 4817-4825

出版社

DOVE MEDICAL PRESS LTD
DOI: 10.2147/JIR.S328732

关键词

intestinal ischemia-reperfusion injury; microRNA; prognostic marker; bioinformatics

资金

  1. National Natural Science Foundation of China [81801943]
  2. Science and Technology Commission of Shanghai Municipality [18411970200]
  3. Research Grant for Public Health Key Discipline of Shanghai Municipality, China [No.GWV-10.1-XK26]

向作者/读者索取更多资源

In this study, a regulatory network between miRNA and mRNA in intestinal ischemia-reperfusion injury was demonstrated. Key mRNAs and their potential functions were explored through functional analysis, providing new insights for prognostic markers and therapeutic targets in clinical practice for patients with this condition.
Background: Intestinal ischemia-reperfusion (II/R) injury is a common clinical complication associated with high mortality, for which microRNA (miRNA) drives potentially its pathophysiological progression. MiRNAs regulate different messenger RNAs (mRNAs). However, the regulatory network between miRNAs and mRNAs in intestinal ischemiareperfusion injury is elusive Methods: We analyzed the different expression of mRNAs and miRNAs in intestinal tissues from patients from three groups (arterial group (group A), venous group (group V), control group (group C)). Common differentially expressed (Co-DE) miRNAs and differentially expressed mRNAs were acquired via concerned analyses among the three groups. Co-DE mRNAs were shared parts of target mRNAs and differentially expression mRNAs. Cytoscape was employed to construct the regulatory network between miRNAs and mRNAs. Gene Ontology (GO) analysis and the Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway depicted the functions and potential pathway associated with Co-DE mRNAs. Using the STRING and Cytoscape, we found critical mRNAs in the protein-protein interaction (PPI) network Results: The miRNA-mRNA network comprised 8 Co-DE miRNAs and 140 Co-DE mRNAs. Of note, 140 Co-DE mRNAs were targets of these 8 miRNAs, and their roles were established through the functional exploration via GO analysis and KEGG analysis. PPI network and Cytoscape revealed COL1A2, THY1, IL10, MMP2, SERPINH1, COL3A1, COL14A1, and P4HA1 as the top 8 key mRNAs. Conclusion: This study has demonstrated a miRNA-mRNA regulatory network in intestinal ischemia-reperfusion injury, and explored the key mRNAs and their potential functions. These findings could provide new insight into prognostic markers and therapeutic targets for patients with intestinal ischemia-reperfusion injury in clinical practice.

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