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pmid:32696819

Identification of potential molecular mechanisms and small molecule drugs in myocardial ischemia/reperfusion injury.

Tao Jiang · Yingcun Liu · Biao Chen · Liangyi Si

Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2020 doi:10.1590/1414-431x20209717

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:32696819
kind
science-record
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sha256:56dacbddaee7062d1a150d6aa392b36fbc1555685a3dc0d0e74571b6f620dd66
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https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json
created_at
2026-11-01T15:41:06Z
updated_at
2026-11-01T22:01:56Z
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paper object · 10 fields
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title
Identification of potential molecular mechanisms and small molecule drugs in myocardial ischemia/reperfusion injury.
doi
10.1590/1414-431x20209717
pmid
32696819
authors array · 4 items
[0]
Tao Jiang
[1]
Yingcun Liu
[2]
Biao Chen
[3]
Liangyi Si
journal
Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica
year
2020
abstract
Myocardial ischemia/reperfusion (MI/R) injury is a complex phenomenon that causes severe damage to the myocardium. However, the potential molecular mechanisms of MI/R injury have not been fully clarified. We identified potential molecular mechanisms and therapeutic targets in MI/R injury through analysis of Gene Expression Omnibus (GEO) database. Differentially expressed genes (DEGs) were found between MI/R injury and normal samples, and overlapping DEGs were found between GSE61592 and GSE67308. Gene Ontology (GO) and pathway analysis were performed for overlapping DEGs by Database for Annotation, Visualization and Integration Discovery (DAVID). Then, a network of protein-protein interaction (PPI) was constructed through the Search Tool for the Retrieval of Interacting Genes (STRING) database. Potential microRNAs (miRNAs) and therapeutic small molecules were screened out using microRNA.org database and the Comparative Toxicogenomics database (CTD), respectively. Finally, we identified 21 overlapping DEGs related to MI/R injury. These DEGs were significantly enriched in IL-17 signaling pathway, cytosolic DNA-sensing pathway, chemokine signaling, and cytokine-cytokine receptor interaction pathway. According to the degree in the PPI network, CCL2, LCN2, HP, CCL7, HMOX1, CCL4, and S100A8 were found to be hub genes. Furthermore, we identified potential miRNAs (miR-24-3p, miR-26b-5p, miR-2861, miR-217, miR-4251, and miR-124-3p) and therapeutic small molecules like ozone, troglitazone, rosiglitazone, and n-3 polyunsaturated fatty acids for MI/R injury. These results identified hub genes and potential small molecule drugs, which could contribute to the understanding of molecular mechanisms and treatment for MI/R injury.
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After data preprocessing, the fold change (FC) of gene expression and the false discovery rate (FDR) was calculated between MI/R and normal samples. DEGs were identified with a |log FC| ≥2 and an FDR <0.05.
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sections[4] "Identification of overlapping DEGs and enrichment analysis" paragraph 2
quote
After data preprocessing, the fold change (FC) of gene expression and the false discovery rate (FDR) was calculated between MI/R and normal samples. DEGs were identified with a |log FC| ≥2 and an FDR <0.05.
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The GSE61592 and GSE67308 datasets were downloaded from the GEO database (http://www.ncbi.nlm.nih.gov/geo/). The GSE61592 dataset included three normal heart samples and three MI/R injury samples. The MI/R injury samples of two datasets were obtained from mice subjected to I/R involving left anterior descending coronary artery occlusion followed by reperfusion.
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sections[3] "Datasets and data preprocessing" paragraph 2
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The GSE61592 and GSE67308 datasets were downloaded from the GEO database (http://www.ncbi.nlm.nih.gov/geo/).
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sections[3] "Datasets and data preprocessing" paragraph 2
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The GSE61592 dataset included three normal heart samples and three MI/R injury samples.
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sections[3] "Datasets and data preprocessing" paragraph 2
quote
The MI/R injury samples of two datasets were obtained from mice subjected to I/R involving left anterior descending coronary artery occlusion followed by reperfusion.
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The GSE61592 and GSE67308 datasets were downloaded from the GEO database (http://www.ncbi.nlm.nih.gov/geo/). The GSE61592 dataset included three normal heart samples and three MI/R injury samples. The MI/R injury samples of two datasets were obtained from mice subjected to I/R involving left anterior descending coronary artery occlusion followed by reperfusion.
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The GSE61592 and GSE67308 datasets were downloaded from the GEO database (http://www.ncbi.nlm.nih.gov/geo/). The GSE61592 dataset included three normal heart samples and three MI/R injury samples. The MI/R injury samples of two datasets were obtained from mice subjected to I/R involving left anterior descending coronary artery occlusion followed by reperfusion.
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title
IGF-1 degradation by mast cell chymase promotes delayed cell death in post-ischemic hearts
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The GSE61592 and GSE67308 datasets were downloaded from the GEO database (http://www.ncbi.nlm.nih.gov/geo/). The GSE61592 dataset included three normal heart samples and three MI/R injury samples. The MI/R injury samples of two datasets were obtained from mice subjected to I/R involving left anterior descending coronary artery occlusion followed by reperfusion.
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Hif2a-cardiomyocyte deficient mice response to myocardial ischemia and reperfusion
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identifier_resolution_only_no_download_no_licence_read
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GO functional annotation and pathway enrichment analysis in overlapping DEGs
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Table 1
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Kyoto Encyclopedia of Genes and Genomes pathway enrichment analysis of overlapping DEGs.
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[0] array · 4 items
[0]
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FDR
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[0]
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[3]
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[2] array · 4 items
[0]
Chemokine signaling pathway
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0.0112
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3
[3]
CCL2, CCL4, CCL7
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Cytokine-cytokine receptor interaction
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3
[3]
CCL2, CCL4, CCL7
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Cytosolic DNA-sensing pathway
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section[9]/table-wrap[1]#t01
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Construction of PPI network and identification of hub genes
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Table 2
caption
Protein-protein interaction network degree of identified hub genes.
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Up/down
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7.911
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Up
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Up
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HP
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3.833
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CCL7
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3.611
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Up
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HMOX1
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Up
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CCL4
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3.120
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3.018
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Up
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section[10]/table-wrap[1]#t02
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Potential microRNAs of overlapping DEGs.
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11
section_title
Potential miRNAs and small molecules associated with MI/R injury
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Table 3
caption
Potential microRNAs of overlapping DEGs.
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[0] array · 4 items
[0]
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Gene count
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Target genes
[1] array · 4 items
[0]
miR-24-3p
[1]
1.93E-02
[2]
4
[3]
S100A8, CCL2, CCL4, HMOX1
[2] array · 4 items
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miR-26b-5p
[1]
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[2]
5
[3]
CCL2, CCL7, PLAC8, HMOX1, CH25H
[3] array · 4 items
[0]
miR-2861
[1]
2.91E-02
[2]
3
[3]
AIF1, ANGPTL4, LCN2
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[0]
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[1]
3.60E-02
[2]
4
[3]
CLEC4D, CYP1B1, CCL4, HMOX1
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[1]
3.61E-02
[2]
4
[3]
CLEC4D, CCL7, PLAC8, LCN2
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[0]
miR-124-3p
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3.85E-02
[2]
4
[3]
CYP1B1, CCL2, ANGPTL4, HMOX1
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section[11]/table-wrap[1]#t03
[6] object · 16 fields
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Top 20 potential small molecules of the overlapping DEGs.
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PMC7372942
section_index
11
section_title
Potential miRNAs and small molecules associated with MI/R injury
row_count
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table object · 8 fields
label
Table 4
caption
Top 20 potential small molecules of the overlapping DEGs.
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[0] array · 4 items
[0]
Molecule in CTD
[1]
FDR
[2]
Gene count
[3]
Target gene
[1] array · 4 items
[0]
Quartz
[1]
4.99E-10
[2]
7
[3]
S100A9, HP, CCL2, CCL7, HMOX1, LCN2, CH25H
[2] array · 4 items
[0]
Pregnenolone carbonitrile
[1]
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[2]
13
[3]
CLEC4D, S100A8, AIF1, S100A9, HP, CYP1B1, CCL2, IL33, G0S2, ANGPTL4, HMOX1, LCN2, CH25H
[3] array · 4 items
[0]
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[2]
12
[3]
S100A8, S100A9, CYP1B1, CCL2, CCL4, IL33, CCL7, G0S2, ANGPTL4, HMOX1, LCN2, CH25H
[4] array · 4 items
[0]
Muraglitazar
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9
[3]
AIF1, CCL2, CCL4, IL33, CCL7, G0S2, ANGPTL4, LCN2, CH25H
[5] array · 4 items
[0]
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[2]
7
[3]
S100A8, AIF1, S100A9, HP, CYP1B1, HMOX1, LCN2
[6] array · 4 items
[0]
Dimethylnitrosamine
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10
[3]
AIF1, S100A9, HP, CCL2, IL33, CCL7, PLAC8, G0S2, HMOX1, LCN2
[7] array · 4 items
[0]
Doxorubicin
[1]
5.77E-08
[2]
12
[3]
S100A8, AIF1, S100A9, CYP1B1, CCL2, CCL4, CCL7, PLAC8, G0S2, HMOX1, LCN2, CH25H
[8] array · 4 items
[0]
Troglitazone
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7.00E-08
[2]
11
[3]
HP, CYP1B1, CCL2, CCL4, IL33, CCL7, G0S2, ANGPTL4, HMOX1, LCN2, CH25H
[9] array · 4 items
[0]
Naphthalene
[1]
8.36E-08
[2]
8
[3]
S100A8, S100A9, CYP1B1, CCL2, CCL7, ANGPTL4, HMOX1, CH25H
[10] array · 4 items
[0]
Isoproterenol
[1]
1.26E-07
[2]
10
[3]
CLEC4D, S100A8, AIF1, S100A9, CYP1B1, CCL2, CCL7, HMOX1, LCN2, CH25H
[11] array · 4 items
[0]
Cobalt
[1]
2.36E-07
[2]
7
[3]
CYP1B1, CCL2, CCL4, CCL7, G0S2, ANGPTL4, HMOX1
[12] array · 4 items
[0]
Rosiglitazone
[1]
2.92E-07
[2]
11
[3]
AIF1, HP, CYP1B1, CCL2, CCL4, CCL7, G0S2, ANGPTL4, HMOX1, LCN2, CH25H
[13] array · 4 items
[0]
Tesaglitazar
[1]
3.13E-07
[2]
8
[3]
AIF1, CCL2, CCL4, IL33, G0S2, ANGPTL4, HMOX1, CH25H
[14] array · 4 items
[0]
1-Naphthylisothiocyanate
[1]
6.76E-07
[2]
9
[3]
S100A8, AIF1, S100A9, CCL2, IL33, PLAC8, G0S2, HMOX1, LCN2
[15] array · 4 items
[0]
CI 1044
[1]
6.76E-07
[2]
5
[3]
S100A8, S100A9, CYP1B1, HMOX1, LCN2
[16] array · 4 items
[0]
Trimethyltin
[1]
6.76E-07
[2]
5
[3]
AIF1, CCL2, CCL4, HMOX1, LCN2
[17] array · 4 items
[0]
Chloroprene
[1]
1.22E-06
[2]
10
[3]
S100A8, AIF1, S100A9, CYP1B1, IL33, PLAC8, G0S2, ANGPTL4, HMOX1, CH25H
[18] array · 4 items
[0]
Trinitrobenzenesulfonic acid
[1]
1.69E-06
[2]
7
[3]
S100A8, S100A9, CCL2, CCL4, CCL7, HMOX1, LCN2
[19] array · 4 items
[0]
n-3 Polyunsaturated fatty acids
[1]
2.09E-06
[2]
5
[3]
HP, CYP1B1, CCL2, CCL7, HMOX1
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section[11]/table-wrap[2]#t04
gaps array · 4 items
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asset:data:geo:GSE61592 not downloaded
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[2]
asset:data:geo:GSE67308 not downloaded
[3]
asset:data:geo:GSE67308 licence not read
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quote
After data preprocessing, the fold change (FC) of gene expression and the false discovery rate (FDR) was calculated between MI/R and normal samples. DEGs were identified with a |log FC| ≥2 and an FDR <0.05.
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capability object · 4 fields
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capability:computational_analysis
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basis
The computational analysis is owned. The physical bench the paper used is not, so a physical validation cannot be run here.
data object · 6 fields
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statements array · 1 item
[0]
The GSE61592 and GSE67308 datasets were downloaded from the GEO database (http://www.ncbi.nlm.nih.gov/geo/). The GSE61592 dataset included three normal heart samples and three MI/R injury samples. The MI/R injury samples of two datasets were obtained from mice subjected to I/R involving left anterior descending coronary artery occlusion followed by reperfusion.
basis
The paper names GSE61592, GSE67308 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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asset:table:pmid:32696819:3
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MiniMax-M3.1-Flash
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independence
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:32696819", "kind": "science-record", "revision": 6, "content_hash": "sha256:56dacbddaee7062d1a150d6aa392b36fbc1555685a3dc0d0e74571b6f620dd66", "created_at": "2026-11-01T15:41:06Z", "updated_at": "2026-11-01T22:01:56Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification of potential molecular mechanisms and small molecule drugs in myocardial ischemia/reperfusion injury.", "doi": "10.1590/1414-431x20209717", "pmid": "32696819", "authors": ["Tao Jiang", "Yingcun Liu", "Biao Chen", "Liangyi Si"], "journal": "Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica", "year": 2020, "abstract": "Myocardial ischemia/reperfusion (MI/R) injury is a complex phenomenon that causes severe damage to the myocardium. However, the potential molecular mechanisms of MI/R injury have not been fully clarified. We identified potential molecular mechanisms and therapeutic targets in MI/R injury through analysis of Gene Expression Omnibus (GEO) database. Differentially expressed genes (DEGs) were found between MI/R injury and normal samples, and overlapping DEGs were found between GSE61592 and GSE67308. Gene Ontology (GO) and pathway analysis were performed for overlapping DEGs by Database for Annotation, Visualization and Integration Discovery (DAVID). Then, a network of protein-protein interaction (PPI) was constructed through the Search Tool for the Retrieval of Interacting Genes (STRING) database. Potential microRNAs (miRNAs) and therapeutic small molecules were screened out using microRNA.org database and the Comparative Toxicogenomics database (CTD), respectively. Finally, we identified 21 overlapping DEGs related to MI/R injury. These DEGs were significantly enriched in IL-17 signaling pathway, cytosolic DNA-sensing pathway, chemokine signaling, and cytokine-cytokine receptor interaction pathway. According to the degree in the PPI network, CCL2, LCN2, HP, CCL7, HMOX1, CCL4, and S100A8 were found to be hub genes. Furthermore, we identified potential miRNAs (miR-24-3p, miR-26b-5p, miR-2861, miR-217, miR-4251, and miR-124-3p) and therapeutic small molecules like ozone, troglitazone, rosiglitazone, and n-3 polyunsaturated fatty acids for MI/R injury. These results identified hub genes and potential small molecule drugs, which could contribute to the understanding of molecular mechanisms and treatment for MI/R injury.", "claims": [{"id": "claim-method", "statement": "After data preprocessing, the fold change (FC) of gene expression and the false discovery rate (FDR) was calculated between MI/R and normal samples. 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count", "Target genes"], ["miR-24-3p", "1.93E-02", "4", "S100A8, CCL2, CCL4, HMOX1"], ["miR-26b-5p", "1.93E-02", "5", "CCL2, CCL7, PLAC8, HMOX1, CH25H"], ["miR-2861", "2.91E-02", "3", "AIF1, ANGPTL4, LCN2"], ["miR-217", "3.60E-02", "4", "CLEC4D, CYP1B1, CCL4, HMOX1"], ["miR-4251", "3.61E-02", "4", "CLEC4D, CCL7, PLAC8, LCN2"], ["miR-124-3p", "3.85E-02", "4", "CYP1B1, CCL2, ANGPTL4, HMOX1"]], "row_count": 7, "column_count": 4, "numeric_cells": 20, "header_rows": 1, "locator": "section[11]/table-wrap[1]#t03"}}, {"id": "asset:table:pmid:32696819:4", "role": "table", "format": "jats-table", "media_type": "application/vnd.jats.table+json", "uri": null, "sha256": "sha256:5a18c8ab4d88cf53939355650afcd553d7cffb8c5109c2f345707a574bc4e3a6", "bytes": 2056, "access": "open", "state": "verified", "reader": "read_table", "reader_status": "available", "identifier": "section[11]/table-wrap[2]#t04", "version": null, "note": "Top 20 potential small molecules of the overlapping DEGs.", "structure": {"pmcid": "PMC7372942", "section_index": 11, "section_title": "Potential miRNAs and small molecules associated with MI/R injury", "row_count": 20, "column_count": 4}, "table": {"label": "Table 4", "caption": "Top 20 potential small molecules of the overlapping DEGs.", "rows": [["Molecule in CTD", "FDR", "Gene count", "Target gene"], ["Quartz", "4.99E-10", "7", "S100A9, HP, CCL2, CCL7, HMOX1, LCN2, CH25H"], ["Pregnenolone carbonitrile", "4.99E-10", "13", "CLEC4D, S100A8, AIF1, S100A9, HP, CYP1B1, CCL2, IL33, G0S2, ANGPTL4, HMOX1, LCN2, CH25H"], ["Ozone", "2.40E-09", "12", "S100A8, S100A9, CYP1B1, CCL2, CCL4, IL33, CCL7, G0S2, ANGPTL4, HMOX1, LCN2, CH25H"], ["Muraglitazar", "5.64E-09", "9", "AIF1, CCL2, CCL4, IL33, CCL7, G0S2, ANGPTL4, LCN2, CH25H"], ["Hexachlorobenzene", "2.78E-08", "7", "S100A8, AIF1, S100A9, HP, CYP1B1, HMOX1, LCN2"], ["Dimethylnitrosamine", "4.03E-08", "10", "AIF1, S100A9, HP, CCL2, IL33, CCL7, PLAC8, G0S2, HMOX1, LCN2"], ["Doxorubicin", "5.77E-08", "12", "S100A8, AIF1, S100A9, CYP1B1, CCL2, CCL4, CCL7, PLAC8, G0S2, HMOX1, LCN2, CH25H"], ["Troglitazone", "7.00E-08", "11", "HP, CYP1B1, CCL2, CCL4, IL33, CCL7, G0S2, ANGPTL4, HMOX1, LCN2, CH25H"], ["Naphthalene", "8.36E-08", "8", "S100A8, S100A9, CYP1B1, CCL2, CCL7, ANGPTL4, HMOX1, CH25H"], ["Isoproterenol", "1.26E-07", "10", "CLEC4D, S100A8, AIF1, S100A9, CYP1B1, CCL2, CCL7, HMOX1, LCN2, CH25H"], ["Cobalt", "2.36E-07", "7", "CYP1B1, CCL2, CCL4, CCL7, G0S2, ANGPTL4, HMOX1"], ["Rosiglitazone", "2.92E-07", "11", "AIF1, HP, CYP1B1, CCL2, CCL4, CCL7, G0S2, ANGPTL4, HMOX1, LCN2, CH25H"], ["Tesaglitazar", "3.13E-07", "8", "AIF1, CCL2, CCL4, IL33, G0S2, ANGPTL4, HMOX1, CH25H"], ["1-Naphthylisothiocyanate", "6.76E-07", "9", "S100A8, AIF1, S100A9, CCL2, IL33, PLAC8, G0S2, HMOX1, LCN2"], ["CI 1044", "6.76E-07", "5", "S100A8, S100A9, CYP1B1, HMOX1, LCN2"], ["Trimethyltin", "6.76E-07", "5", "AIF1, CCL2, CCL4, HMOX1, LCN2"], ["Chloroprene", "1.22E-06", "10", "S100A8, AIF1, S100A9, CYP1B1, IL33, PLAC8, G0S2, 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