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pmid:31545397

Screening and identification of biomarkers for systemic sclerosis via microarray technology.

Chen Xu · Ling-Bing Meng · Yu-Chen Duan · Yong-Jing Cheng · Chun-Mei Zhang · Xing Zhou · Ci-Bo Huang

International journal of molecular medicine · 2019 doi:10.3892/ijmm.2019.4332

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complete

Experiment

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Data

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Analysis

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:31545397
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title
Screening and identification of biomarkers for systemic sclerosis via microarray technology.
doi
10.3892/ijmm.2019.4332
pmid
31545397
authors array · 7 items
[0]
Chen Xu
[1]
Ling-Bing Meng
[2]
Yu-Chen Duan
[3]
Yong-Jing Cheng
[4]
Chun-Mei Zhang
[5]
Xing Zhou
[6]
Ci-Bo Huang
journal
International journal of molecular medicine
year
2019
abstract
Systemic sclerosis (SSc) is a complex autoimmune disease. The pathogenesis of SSc is currently unclear, although like other rheumatic diseases its pathogenesis is complicated. However, the ongoing development of bioinformatics technology has enabled new approaches to research this disease using microarray technology to screen and identify differentially expressed genes (DEGs) in the skin of patients with SSc compared with individuals with healthy skin. Publicly available data were downloaded from the Gene Expression Omnibus (GEO) database and intra‑group data repeatability tests were conducted using Pearson's correlation test and principal component analysis. DEGs were identified using an online tool, GEO2R. Functional annotation of DEGs was performed using Gene Ontology (GO) and the Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis. Finally, the construction and analysis of the protein‑protein interaction (PPI) network and identification and analysis of hub genes was carried out. A total of 106 DEGs were detected by the screening of SSc and healthy skin samples. A total of 10 genes [interleukin‑6, bone morphogenetic protein 4, calumenin (CALU), clusterin, cysteine rich angiogenic inducer 61, serine protease 23, secretogranin II, suppressor of cytokine signaling 3, Toll‑like receptor 4 (TLR4), tenascin C] were identified as hub genes with degrees ≥10, and which could sensitively and specifically predict SSc based on receiver operator characteristic curve analysis. GO and KEGG analysis showed that variations in hub genes were mainly enriched in positive regulation of nitric oxide biosynthetic processes, negative regulation of apoptotic processes, extracellular regions, extracellular spaces, cytokine activity, chemo‑attractant activity, and the phosphoinositide 3 kinase‑protein kinase B signaling pathway. In summary, bioinformatics techniques proved useful for the screening and identification of biomarkers of disease. A total of 106 DEGs and 10 hub genes were linked to SSc, in particular the TLR4 and CALU genes.
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The limma (Linear Models for Microarray Analysis) R package, which could perform the paired-samples T test, has emerged as one of the most widely used statistical tests for identifying differentially expressed genes (17).
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The limma (Linear Models for Microarray Analysis) R package, which could perform the paired-samples T test, has emerged as one of the most widely used statistical tests for identifying differentially expressed genes (17).
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sections[20] "Availability of data and materials" paragraph 2
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The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
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Systemic sclerosis skin disease trajectory during mycophenolate mofetil treatment
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lineage object · 4 fields
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gaps array · 9 items
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asset:data:geo:GSE76885 licence not read
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evidence array · 2 items
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ion of biomarkers for systemic sclerosis via microarray technology.
[1]
ew approaches to research this disease using microarray technology to screen and identify differenti
order_basis
paper_text_order:25
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assay:1
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role
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required_operations array · 3 items
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fdr_bh
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source_hashes object · 1 field
dsl_catalogue
f2132e96ae6c7a4e
evidence array · 1 item
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The limma (Linear Models for Microarray Analysis) R package, which could perform the paired-samples T test, has emerged as one of the most widely used statistical tests for identifying differentially expressed genes (17).
order_basis
consumes_earlier_output
id
assay:2
Complete file
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However, the ongoing development of bioinformatics technology has enabled new approaches to research this disease using microarray technology to screen and identify differentially expressed genes (DEGs) in the skin of patients with SSc compared with individuals with healthy skin. Publicly available data were downloaded from the Gene Expression Omnibus (GEO) database and intra‑group data repeatability tests were conducted using Pearson's correlation test and principal component analysis. DEGs were identified using an online tool, GEO2R. Functional annotation of DEGs was performed using Gene Ontology (GO) and the Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis. Finally, the construction and analysis of the protein‑protein interaction (PPI) network and identification and analysis of hub genes was carried out. A total of 106 DEGs were detected by the screening of SSc and healthy skin samples. 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