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pmid:34475773

Bioinformatics Analysis for Identification of Key Genes in Salivary Gland and the Potential of a Combination of Biomarkers for the Diagnosis of SS.

Liying Chen · Dingqi Lu · Kai Yu · Shiya He · Liu Liu · Xvfeng Zhang · Bo Feng · Xinchang Wang

Journal of inflammation research · 2021 doi:10.2147/JIR.S322318

Paper

complete

Experiment

partial

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:34475773
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science-record
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https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json
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2026-11-01T15:41:50Z
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2026-11-01T22:04:38Z
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paper object · 10 fields
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title
Bioinformatics Analysis for Identification of Key Genes in Salivary Gland and the Potential of a Combination of Biomarkers for the Diagnosis of SS.
doi
10.2147/JIR.S322318
pmid
34475773
authors array · 8 items
[0]
Liying Chen
[1]
Dingqi Lu
[2]
Kai Yu
[3]
Shiya He
[4]
Liu Liu
[5]
Xvfeng Zhang
[6]
Bo Feng
[7]
Xinchang Wang
journal
Journal of inflammation research
year
2021
abstract
PURPOSE: Sjögren's syndrome (SS) is a systemic autoimmune disease mainly characterized by dysfunction of exocrine glands. Studies on diagnosis models specific for SS patients are very limited. We aimed to use gene expression datasets from salivary glands to identify aberrant differentially expressed genes (DEGs) and pathways by bioinformatics and validate candidate genes by clinical minor labial gland biopsy (MSGB) samples, and finally build a combined gene quantitative diagnosis model of SS. PATIENTS AND METHODS: Original datasets GSE23117, GSE7451, and GSE127952 were obtained from the Gene Expression Omnibus database (GEO) and integrated and analyzed for differentially expressed genes in SS salivary glands. ClueGO and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analyses of upregulated and downregulated DEGs were performed, and protein-protein interaction (PPI) networks were constructed using the STRING and Cytoscape database. H&E staining and immunohistochemistry were used to validate the expression levels of four hub genes in salivary glands. Finally, a receiver operating characteristic (ROC) curve of the combined diagnosis of four hub genes was analyzed in SS patients and non-SS patients in order to explore the diagnostic efficacy of these genes compared with conventional FS in SS. RESULTS: Fifty-three upregulated genes and fifteen downregulated genes were identified. We analyzed the expression and function of four hub genes via H&E, immunohistochemistry, and ROC analysis. We then evaluated and verified the diagnosis value of four hub genes, STAT1, MNDA, IL10RA, and CCR1 in MSGB of SS and non-SS. A combined diagnosis model of four indicators was established to identify patients' discrete data on the foci size (AUC=0.915). CONCLUSION: The expression of STAT1, MNDA, and IL10RA may be potential biological indicators for SS diagnosis. Compared with FS, a combined diagnosis model of quantitative gene expression could potentially contribute to improving the sensitivity and specificity of MSGB of SS.
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Wilcoxon Mann–Whitney U two-sample rank sum test was used to analyze the statistical significance between two groups.
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The salivary gland gene expression profiles of GSE23117 (n = 4 control, n = 11 SS), GSE7451 (n = 10 control, n = 10 SS), and GSE127952 (n = 6 control, n = 8 SS) were obtained from NCBI-GEO (https://www.ncbi.nlm.nih.gov/), which together included 20 healthy controls and 29 SS patients.
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sections[3] "Microarray Datasets and the Identification of Differentially Expressed Genes (DEGs)" paragraph 2
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The salivary gland gene expression profiles of GSE23117 (n = 4 control, n = 11 SS), GSE7451 (n = 10 control, n = 10 SS), and GSE127952 (n = 6 control, n = 8 SS) were obtained from NCBI-GEO (https://www.ncbi.nlm.nih.gov/), which together included 20 healthy controls and 29 SS patients.
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Primary Sjogren's syndrome and control whole saliva
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Validation of Hub Genes and Evaluation of Their Efficacy Using Hematoxylin and Eosin (H&E) and Immunohistochemistry
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The salivary gland gene expression profiles of GSE23117 (n = 4 control, n = 11 SS), GSE7451 (n = 10 control, n = 10 SS), and GSE127952 (n = 6 control, n = 8 SS) were obtained from NCBI-GEO (https://www.ncbi.nlm.nih.gov/), which together included 20 healthy controls and 29 SS patients.
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sion and function of four hub genes via H&E, immunohistochemistry, and ROC analysis. We then evaluated and ver
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evidence array · 1 item
[0]
Wilcoxon Mann–Whitney U two-sample rank sum test was used to analyze the statistical significance between two groups.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:34475773", "kind": "science-record", "revision": 8, "content_hash": "sha256:d0737e5259ecf7f744ef59b01978327d5c98cd90aab58baf83d12198b336422c", "created_at": "2026-11-01T15:41:50Z", "updated_at": "2026-11-01T22:04:38Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Bioinformatics Analysis for Identification of Key Genes in Salivary Gland and the Potential of a Combination of Biomarkers for the Diagnosis of SS.", "doi": "10.2147/JIR.S322318", "pmid": "34475773", "authors": ["Liying Chen", "Dingqi Lu", "Kai Yu", "Shiya He", "Liu Liu", "Xvfeng Zhang", "Bo Feng", "Xinchang Wang"], "journal": "Journal of inflammation research", "year": 2021, "abstract": "PURPOSE: Sjögren's syndrome (SS) is a systemic autoimmune disease mainly characterized by dysfunction of exocrine glands. Studies on diagnosis models specific for SS patients are very limited. We aimed to use gene expression datasets from salivary glands to identify aberrant differentially expressed genes (DEGs) and pathways by bioinformatics and validate candidate genes by clinical minor labial gland biopsy (MSGB) samples, and finally build a combined gene quantitative diagnosis model of SS.\nPATIENTS AND METHODS: Original datasets GSE23117, GSE7451, and GSE127952 were obtained from the Gene Expression Omnibus database (GEO) and integrated and analyzed for differentially expressed genes in SS salivary glands. ClueGO and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analyses of upregulated and downregulated DEGs were performed, and protein-protein interaction (PPI) networks were constructed using the STRING and Cytoscape database. H&E staining and immunohistochemistry were used to validate the expression levels of four hub genes in salivary glands. Finally, a receiver operating characteristic (ROC) curve of the combined diagnosis of four hub genes was analyzed in SS patients and non-SS patients in order to explore the diagnostic efficacy of these genes compared with conventional FS in SS.\nRESULTS: Fifty-three upregulated genes and fifteen downregulated genes were identified. We analyzed the expression and function of four hub genes via H&E, immunohistochemistry, and ROC analysis. We then evaluated and verified the diagnosis value of four hub genes, STAT1, MNDA, IL10RA, and CCR1 in MSGB of SS and non-SS. A combined diagnosis model of four indicators was established to identify patients' discrete data on the foci size (AUC=0.915).\nCONCLUSION: The expression of STAT1, MNDA, and IL10RA may be potential biological indicators for SS diagnosis. 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This lane did not download the dataset or read its licence.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE127952"], "outputs": ["the source data with its repository provenance"], "instruments": [], "reagents": []}, {"id": "run_analysis", "order": 3, "name": "Run the published analysis", "kind": "analysis", "state": "blocked", "blocked_on": "method:group_comparison_wilcoxon", "description": "Apply the paper's statistical method to the resolved series and compare the result with the published target.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE127952"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": ["step:run_analysis blocked on method:group_comparison_wilcoxon"]}, "data": {"state": "partial", "assets": [{"id": "source:pmid:34475773", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": 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control, n = 11 SS), GSE7451 (n = 10 control, n = 10 SS), and GSE127952 (n = 6 control, n = 8 SS) were obtained from NCBI-GEO (https://www.ncbi.nlm.nih.gov/), which together included 20 healthy controls and 29 SS patients.", "structure": {"repository": "GEO", "access_route": "GEO accession URL", "access_statement_verbatim": "The salivary gland gene expression profiles of GSE23117 (n = 4 control, n = 11 SS), GSE7451 (n = 10 control, n = 10 SS), and GSE127952 (n = 6 control, n = 8 SS) were obtained from NCBI-GEO (https://www.ncbi.nlm.nih.gov/), which together included 20 healthy controls and 29 SS patients.", "access_statement_kind": "repository_route_statement", "sample_accessions": ["GSM3657186", "GSM3657187", "GSM3657188", "GSM3657189", "GSM3657190", "GSM3657191", "GSM3657192", "GSM3657193", "GSM3657194", "GSM3657195", "GSM3657196", "GSM3657197", "GSM3657198", "GSM3657199"], "sample_count": 14, "group_sizes": null, "group_sizes_basis": null, "platform": "20995", "taxon": "Homo 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