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pmid:39028999

Integrative analysis of gene and microRNA expression profiles reveals candidate biomarkers and regulatory networks in psoriasis.

Lu Chen · Xiaochen Wang · Chang Liu · Xiaoqing Chen · Peng Li · Wenhong Qiu · Kaiwen Guo

Medicine · 2024 doi:10.1097/MD.0000000000039002

Paper

complete

Experiment

complete

Data

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Analysis

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Execution

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:39028999
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science-record
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2026-11-01T20:29:06Z
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2026-11-01T22:54:44Z
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paper object · 10 fields
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title
Integrative analysis of gene and microRNA expression profiles reveals candidate biomarkers and regulatory networks in psoriasis.
doi
10.1097/MD.0000000000039002
pmid
39028999
authors array · 7 items
[0]
Lu Chen
[1]
Xiaochen Wang
[2]
Chang Liu
[3]
Xiaoqing Chen
[4]
Peng Li
[5]
Wenhong Qiu
[6]
Kaiwen Guo
journal
Medicine
year
2024
abstract
Psoriasis (PS) is a chronic inflammatory skin disease with a long course and tendency to recur, the pathogenesis of which is not fully understood. This article aims to identify the key differentially expressed genes (DEGs) and microRNA (miRNAs) of PS, construct the core miRNA-mRNA regulatory network, and investigate the underlying molecular mechanism through integrated bioinformatics approaches. Two gene expression profile datasets and 2 miRNA expression profile datasets were downloaded from the gene expression omnibus (GEO) database and analyzed by GEO2R. Intersection DEGs and intersection differentially expressed miRNAs (DEMs) were each screened. The Metascape database and R software were used to perform enrichment analysis of intersecting DEGs and study their functions. Target genes of DEMs were predicted from the online database miRNet. The protein-protein interaction files of the overlapping target genes were obtained from string and the miRNA-mRNA network was constructed by Cytoscape software. In addition, the online web tool CIBERSORT was used to analyze the immune infiltration of dataset GSE166388, and the relative abundance of 22 immune cells in the diseased and normal control tissues was calculated and assessed. Finally, quantitative reverse transcription polymerase chain reaction (qRT-PCR) was used to verify the relative expression of the screened miRNAs and mRNAs to assess the applicability of DEMs and DEGs as biomarkers in PS. A total of 205 mating DEGs and 6 mating DEMs were screened. 103 dysregulated crossover genes from 205 crossover DEGs and 7878 miRNA target genes were identified. The miRNA-mRNA regulatory network was constructed and the top 10 elements were obtained from CytoHubba, including hsa-miR-146a-5p, hsa-miR-17-5p, hsa-miR-106a-5p, hsa-miR-18a-5p, CDK1, CCNA2, CCNB1, MAD2L1, RRM2, and CCNB2. QRT-PCR revealed significant differences in miRNA and gene expression between inflammatory and normal states. In this study, the miRNA-mRNA core regulator pairs hsa-miR-146a-5p, hsa-miR-17-5p, hsa-miR-106a-5p, hsa-miR-18a-5p, CDK1, CCNA2, CCNB1, MAD2L1, RRM2, and CCNB2 may be involved in the course of PS. This study provides new insights to discover new potential targets and biomarkers to further investigate the molecular mechanism of PS.
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GEO2R (http://www.ncbi.nlm.nih.gov/geo/geo2r/) is an online, interactive tool based on the Limma package to identify DEGs by comparing samples from the GEO series.
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sections[4] "2.2. Identification of DEGs and DEMs" paragraph 2
quote
GEO2R (http://www.ncbi.nlm.nih.gov/geo/geo2r/) is an online, interactive tool based on the Limma package to identify DEGs by comparing samples from the GEO series.
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sections[24] "fn-group" paragraph 1
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The datasets generated during and/or analyzed during the current study are publicly available.
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The analysis identified 205 overlapping differentially expressed genes and 6 overlapping differentially expressed miRNAs in psoriasis datasets.
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sections[13] "3.1. Identification of DEGs in PS" paragraph 2
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A total of 547 DEGs (366 upregulated and 181 downregulated mRNAs) and 2232 DEGs (1108 upregulated and 1124 downregulated mRNAs) were screened from the GSE166388 and GSE153007 data sets, respectively.
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sections[13] "3.1. Identification of DEGs in PS" paragraph 2
quote
In addition, the online bioinformatics tool VENNY 2.1.0 was used to obtain 205 slice DEGs, including 159 upregulated mRNAs and 46 downregulated mRNAs (Fig. 1E).
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sections[15] "3.3. Identification of DEMs in PS" paragraph 2
quote
Furthermore, after using the online bioinformatics tool VENNY 2.1.0 to obtain the intersection, 6 DEMs were selected from the 2 datasets that were both upregulated (Fig. 5E, Table 2).
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The analysis identified 205 overlapping differentially expressed genes and 6 overlapping differentially expressed miRNAs in psoriasis datasets.
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zed HaCaT cells (Procell, Wuhan, China) were cultured in a complete medium supplemented with 10% FBS
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Complete file
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This article aims to identify the key differentially expressed genes (DEGs) and microRNA (miRNAs) of PS, construct the core miRNA-mRNA regulatory network, and investigate the underlying molecular mechanism through integrated bioinformatics approaches. Two gene expression profile datasets and 2 miRNA expression profile datasets were downloaded from the gene expression omnibus (GEO) database and analyzed by GEO2R. Intersection DEGs and intersection differentially expressed miRNAs (DEMs) were each screened. The Metascape database and R software were used to perform enrichment analysis of intersecting DEGs and study their functions. Target genes of DEMs were predicted from the online database miRNet. The protein-protein interaction files of the overlapping target genes were obtained from string and the miRNA-mRNA network was constructed by Cytoscape software. In addition, the online web tool CIBERSORT was used to analyze the immune infiltration of dataset GSE166388, and the relative abundance of 22 immune cells in the diseased and normal control tissues was calculated and assessed. Finally, quantitative reverse transcription polymerase chain reaction (qRT-PCR) was used to verify the relative expression of the screened miRNAs and mRNAs to assess the applicability of DEMs and DEGs as biomarkers in PS. A total of 205 mating DEGs and 6 mating DEMs were screened. 103 dysregulated crossover genes from 205 crossover DEGs and 7878 miRNA target genes were identified. The miRNA-mRNA regulatory network was constructed and the top 10 elements were obtained from CytoHubba, including hsa-miR-146a-5p, hsa-miR-17-5p, hsa-miR-106a-5p, hsa-miR-18a-5p, CDK1, CCNA2, CCNB1, MAD2L1, RRM2, and CCNB2. QRT-PCR revealed significant differences in miRNA and gene expression between inflammatory and normal states. In this study, the miRNA-mRNA core regulator pairs hsa-miR-146a-5p, hsa-miR-17-5p, hsa-miR-106a-5p, hsa-miR-18a-5p, CDK1, CCNA2, CCNB1, MAD2L1, RRM2, and CCNB2 may be involved in the course of PS. This study provides new insights to discover new potential targets and biomarkers to further investigate the molecular mechanism of PS.", "claims": [{"id": "claim-method", "statement": "GEO2R (http://www.ncbi.nlm.nih.gov/geo/geo2r/) is an online, interactive tool based on the Limma package to identify DEGs by comparing samples from the GEO series.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:39028999", "locator": "sections[4] \"2.2. 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