已发表论文

识别唾液腺关键基因的生物信息学分析和生物标志物组合诊断干燥综合征(SS)的潜力

 

Authors Chen L, Lu D, Yu K, He S, Liu L, Zhang X, Feng B, Wang X

Received 28 May 2021

Accepted for publication 9 August 2021

Published 25 August 2021 Volume 2021:14 Pages 4143—4153

DOI https://doi.org/10.2147/JIR.S322318

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 2

Editor who approved publication: Dr Monika Sharma

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.
Keywords: Sjogren’s syndrome, bioinformatics analysis, hub genes, validation, diagnostic performance, focus score