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pmid:36536067

Identifying differentially expressed genes and miRNAs in Kawasaki disease by bioinformatics analysis.

Yanliang Cai · Weitao Hu

Scientific reports · 2022 doi:10.1038/s41598-022-26608-x

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complete

Experiment

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Identifying differentially expressed genes and miRNAs in Kawasaki disease by bioinformatics analysis.
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10.1038/s41598-022-26608-x
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36536067
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Yanliang Cai
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Weitao Hu
journal
Scientific reports
year
2022
abstract
Kawasaki disease (KD) is an acute systemic immune vasculitis caused by infection, and its etiology and underlying mechanisms are not completely clear. This study aimed to identify differentially expressed genes (DEGs) with diagnostic and treatment potential for KD using bioinformatics analysis. In this study, three KD datasets (GSE68004, GSE73461, GSE18606) were downloaded from the Gene Expression Omnibus (GEO) database. Identification of DEGs between normal and KD whole blood was performed using the GEO2R online tool. Gene ontology and Kyoto Encyclopedia of Genes and Genomes (KEGG) functional enrichment analysis of DEGs was undertaken with Metascape. Analysis and visualization of protein-protein interaction networks (PPI) were carried out with STRING and Cytoscape. Lastly, miRNA-genes regulatory networks were built by Cytoscape to predict the underlying microRNAs (miRNAs) associated with DEGs. Overall, 269 DEGs were identified, including 230 up-regulated and 39 down-regulated genes. The enrichment functions and pathways of DEGs involve regulation of defense response, inflammatory response, response to bacterium, and T cell differentiation. KEGG analysis indicates that the genes were significantly enriched in Neutrophil extracellular trap formation, TNF signaling pathway, Cytokine-cytokine receptor interaction, and Primary immunodeficiency. After combining the results of the protein-protein interaction (PPI) network and CytoHubba, 9 hub genes were selected, including TLR8, ITGAX, HCK, LILRB2, IL1B, FCGR2A, S100A12, SPI1, and CD8A. Based on the DEGs-miRNAs network construction, 3 miRNAs including mir-126-3p, mir-375 and mir-146a-5p were determined to be potential key miRNAs. To summarize, a total of 269 DEGs, 9 hub genes and 3 miRNAs were identified, which could be considered as KD biomarkers. However, further studies are needed to clarify the biological roles of these genes in KD.
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The adjusted P-values (adj. P) and Benjamini and Hochberg false discovery rate were used to strike a balance between finding statistically significant genes and limiting false positives.
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The adjusted P-values (adj. P) and Benjamini and Hochberg false discovery rate were used to strike a balance between finding statistically significant genes and limiting false positives.
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The datasets generated and/or analyzed during the current study are available in the [GEO] repository, [https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE68004/GSE73461/GSE18606].
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Using GEO2R to analyze three GEO whole-blood microarray datasets, the study identified 269 DEGs, comprising 230 up-regulated and 39 down-regulated genes.
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Overall, 269 DEGs were identified, including 230 up-regulated and 39 down-regulated genes.
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Using GEO2R to analyze three GEO whole-blood microarray datasets, the study identified 269 DEGs, comprising 230 up-regulated and 39 down-regulated genes.
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sample_count
459
group_sizes
null
group_sizes_basis
null
platform
10558
taxon
Homo sapiens
title
Diagnosis of Kawasaki Disease in children using host RNA expression [Discovery_Dataset]
resolution_checked_at
2026-11-01T18:46:34Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
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[3]
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[4]
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[5]
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analysis object · 4 fields
state
partial
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[0] object · 10 fields
id
method-1
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network_analysis
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label
Network / pathway analysis
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build_graph
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protein-protein interaction
[1] object · 10 fields
id
method-2
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null
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null
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Benjamini and Hochberg false discovery rate
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evidence object · 3 fields
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1
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The adjusted P-values (adj. P) and Benjamini and Hochberg false discovery rate were used to strike a balance between finding statistically significant genes and limiting false positives.
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gaps array · 1 item
[0]
method.reader_named_unmapped
capability object · 3 fields
state
complete
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[0] object · 6 fields
capability_id
capability:computational_analysis
label
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[0]
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[1]
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[4]
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[5]
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[6]
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[7]
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[8]
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candidate
Automated Assays Laravel application and simulated adapters
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complete
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R1
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nothing:replicable_now
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pathway_enrich
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basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: ppi_network.
capability object · 4 fields
tier
R1
capability_id
capability:computational_analysis
availability_state
owned
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
tier
R1
reachable
true
accessions array · 3 items
[0]
GSE68004
[1]
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[2]
GSE18606
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[0]
GSE68004
[1]
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[2]
GSE18606
statements array · 1 item
[0]
The datasets generated and/or analyzed during the current study are available in the [GEO] repository, [https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE68004/GSE73461/GSE18606].
basis
The paper names GSE68004, GSE73461, GSE18606 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
can_run object · 3 fields
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run_analysis
must_build object · 5 fields
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[0]
data:geo:GSE18606
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review object · 5 fields
state
partial
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kind
extraction_review
reader object · 5 fields
model
MiniMax-M3.1-Flash
provider
minimax
provider_family
minimax
read_at
2026-11-01T18:20:15Z
independence
single_reader
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method
verbatim
availability
verbatim
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5
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9997
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1286
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128
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[0] object · 4 fields
id
extraction
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complete
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MiniMax-M3.1-Flash
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minimax
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[1]
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absent
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not_run
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null
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pmid:36536067
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paper
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pmid:36536067
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source:pmid:36536067
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manuscript
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PMID 36536067 full text
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data:geo:GSE18606
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dataset
label
GEO GSE18606
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[0] object · 4 fields
id
activity-reading-sci-2026-11-01
type
classification
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pmid:36536067
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paper
label
pmid:36536067
[1] object · 3 fields
id
source:pmid:36536067
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manuscript
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PMID 36536067 full text
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data:geo:GSE18606
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dataset
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GEO GSE18606
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agent:corpus-assay-engine
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activity-read-36536067
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extraction
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agent:minimax-reader
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agent:corpus-assay-engine
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agent:corpus-assay-engine
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software
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Corpus assay engine
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agent:minimax-reader
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MiniMax literature reader
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343fb30756ba6ec3
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pmid:36536067
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sha256:6ab9532795c4ebe5ef23340bd2782560de23101bb06c73c025ce8e92dcf4f6bc
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null
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asset:data:geo:GSE18606 licence not read
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[2]
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[3]
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[4]
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[5]
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[6]
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[7]
method.reader_named_unmapped
[8]
review.human_critique
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[10]
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analysis
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network_analysis
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dsl_catalogue
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:36536067", "kind": "science-record", "revision": 3, "content_hash": "sha256:ff3a25999c91bfa0ecc3b624c7fee771451dba53140f36a117f1acd6ef7feb44", "created_at": "2026-11-01T19:01:03Z", "updated_at": "2026-11-01T22:08:22Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identifying differentially expressed genes and miRNAs in Kawasaki disease by bioinformatics analysis.", "doi": "10.1038/s41598-022-26608-x", "pmid": "36536067", "authors": ["Yanliang Cai", "Weitao Hu"], "journal": "Scientific reports", "year": 2022, "abstract": "Kawasaki disease (KD) is an acute systemic immune vasculitis caused by infection, and its etiology and underlying mechanisms are not completely clear. This study aimed to identify differentially expressed genes (DEGs) with diagnostic and treatment potential for KD using bioinformatics analysis. In this study, three KD datasets (GSE68004, GSE73461, GSE18606) were downloaded from the Gene Expression Omnibus (GEO) database. Identification of DEGs between normal and KD whole blood was performed using the GEO2R online tool. Gene ontology and Kyoto Encyclopedia of Genes and Genomes (KEGG) functional enrichment analysis of DEGs was undertaken with Metascape. Analysis and visualization of protein-protein interaction networks (PPI) were carried out with STRING and Cytoscape. Lastly, miRNA-genes regulatory networks were built by Cytoscape to predict the underlying microRNAs (miRNAs) associated with DEGs. Overall, 269 DEGs were identified, including 230 up-regulated and 39 down-regulated genes. The enrichment functions and pathways of DEGs involve regulation of defense response, inflammatory response, response to bacterium, and T cell differentiation. KEGG analysis indicates that the genes were significantly enriched in Neutrophil extracellular trap formation, TNF signaling pathway, Cytokine-cytokine receptor interaction, and Primary immunodeficiency. After combining the results of the protein-protein interaction (PPI) network and CytoHubba, 9 hub genes were selected, including TLR8, ITGAX, HCK, LILRB2, IL1B, FCGR2A, S100A12, SPI1, and CD8A. Based on the DEGs-miRNAs network construction, 3 miRNAs including mir-126-3p, mir-375 and mir-146a-5p were determined to be potential key miRNAs. To summarize, a total of 269 DEGs, 9 hub genes and 3 miRNAs were identified, which could be considered as KD biomarkers. However, further studies are needed to clarify the biological roles of these genes in KD.", "claims": [{"id": "claim-method", "statement": "The adjusted P-values (adj. P) and Benjamini and Hochberg false discovery rate were used to strike a balance between finding statistically significant genes and limiting false positives.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:36536067", "locator": "sections[4] \"DEGs identification\" paragraph 2", "quote": "The adjusted P-values (adj. 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