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pmid:36091596

Integrated Microarray Analysis to Identify Genes and Small-Molecule Drugs Associated with Stroke Progression.

Shasha Cui · Yunfeng Zhao · Menghui Huang · Huan Zhang · Wei Zhao · Zhenhua Chen

Evidence-based complementary and alternative medicine : eCAM · 2022 doi:10.1155/2022/7634509

Paper

complete

Experiment

complete

Data

partial

Analysis

complete

Execution

absent

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
id
pmid:36091596
kind
science-record
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sha256:39f3ab10fbe43d4d53a5114a05aa8997db73cc169b76526d01954598cf7d73ca
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https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json
created_at
2026-11-01T18:15:19Z
updated_at
2026-11-01T22:50:03Z
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paper object · 10 fields
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title
Integrated Microarray Analysis to Identify Genes and Small-Molecule Drugs Associated with Stroke Progression.
doi
10.1155/2022/7634509
pmid
36091596
authors array · 6 items
[0]
Shasha Cui
[1]
Yunfeng Zhao
[2]
Menghui Huang
[3]
Huan Zhang
[4]
Wei Zhao
[5]
Zhenhua Chen
journal
Evidence-based complementary and alternative medicine : eCAM
year
2022
abstract
Several blood biomarkers are now considered increasingly important for stratifying risk, monitoring disease progression, and evaluating the response to therapy in ischemic stroke. The purpose of the present study was to identify the key genes associated with ischemic stroke progression and elucidate the potential therapeutic small molecules. Microarray datasets related to stroke for GSE58294, GSE22255, and GSE16561 were obtained from the Gene Expression Omnibus (GEO) database. Differentially expressed genes (DEGs) were filtered using the Limma package. DAVID was then searched to perform gene ontology (GO) and pathway enrichment analyses. Based on the DEGs, a protein-protein interaction (PPI) network was developed using Cytoscape, and MCODE was applied to conduct module analysis. Finally, to identify the potential drugs for ischemic stroke, the connectivity map (CMap) database was used. Sixty DEGs were identified after analyzing the three datasets. The GO data analysis revealed that the DEGs were significantly associated with biological processes, including positive regulation of programmed cell death, protein localization in organelles, and positive regulation of apoptosis. KEGG analysis showed that the DEGs were particularly enriched in the Fc epsilon RI signaling pathway, MAPK signaling pathway, and Huntington's disease. We selected five DEGs with high connectivity (CYBB, SYK, DUSP1, TNF, and SP1) that significantly predicted stroke progression. In addition, CMap prediction showed ten small molecules that could be used as adjuvants when treating ischemic stroke. The outcomes of the present study indicated that the five genes mentioned above can be considered potential targets for developing new medications that can modify the ischemic stroke process, and mycophenolic acid was the most promising small molecule to treat ischemic stroke.
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After data analysis with the Limma package, the threshold for identifying DEGs was P < 0.05 [17, 18].
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sections[4] "2.2. Identification of DEGs" paragraph 2
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After data analysis with the Limma package, the threshold for identifying DEGs was P < 0.05 [17, 18].
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6883
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Homo sapiens
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Gene expression analysis of peripheral whole blood RNA following ischemic stroke
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2026-11-01T15:39:54Z
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GSM554053
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Homo sapiens
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Blood genomic expression profile for ischemic stroke (IS)
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2026-11-01T15:39:54Z
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The data can be accessed via GEO database. More details can be obtained from the correspondent authors.
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GSM1406061
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GSM1406062
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GSM1406063
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GSM1406065
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GSM1406066
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GSM1406067
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GSM1406068
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92
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null
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570
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Homo sapiens
title
Gene Expression Following Cardioembolic Stroke
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2026-11-01T15:39:54Z
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Integrated Microarray Analysis to Identify Genes and Small-Molecul
[1]
e the potential therapeutic small molecules. Microarray datasets related to stroke for GSE58294, GSE
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Complete file
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The purpose of the present study was to identify the key genes associated with ischemic stroke progression and elucidate the potential therapeutic small molecules. Microarray datasets related to stroke for GSE58294, GSE22255, and GSE16561 were obtained from the Gene Expression Omnibus (GEO) database. Differentially expressed genes (DEGs) were filtered using the Limma package. DAVID was then searched to perform gene ontology (GO) and pathway enrichment analyses. Based on the DEGs, a protein-protein interaction (PPI) network was developed using Cytoscape, and MCODE was applied to conduct module analysis. Finally, to identify the potential drugs for ischemic stroke, the connectivity map (CMap) database was used. Sixty DEGs were identified after analyzing the three datasets. The GO data analysis revealed that the DEGs were significantly associated with biological processes, including positive regulation of programmed cell death, protein localization in organelles, and positive regulation of apoptosis. KEGG analysis showed that the DEGs were particularly enriched in the Fc epsilon RI signaling pathway, MAPK signaling pathway, and Huntington's disease. We selected five DEGs with high connectivity (CYBB, SYK, DUSP1, TNF, and SP1) that significantly predicted stroke progression. In addition, CMap prediction showed ten small molecules that could be used as adjuvants when treating ischemic stroke. 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