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Identification of immune-related diagnostic markers in primary Sjögren's syndrome based on bioinformatics analysis.

作者信息

Zeng Qingle, Wen Jing, Zheng Leting, Zeng Wen, Chen Shuyuan, Zhao Cheng

机构信息

Department of Rheumatology and Immunology, the First Affiliated Hospital of Guangxi Medical University, Nanning, China.

出版信息

Ann Transl Med. 2022 Apr;10(8):487. doi: 10.21037/atm-22-1494.


DOI:10.21037/atm-22-1494
PMID:35571446
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9096389/
Abstract

BACKGROUND: Primary Sjögren's syndrome (pSS) is a relatively common diffuse connective tissue disease that often invades exocrine glands, such as the lacrimal and salivary glands, and manifests as dry eyes and dry mouth. At present, the molecular mechanism of pSS is not clear. This study was designed to explore the internal mechanism of pSS from the gene level and screen out the immune-related diagnostic markers of pSS. METHODS: The gene expression profiles GSE84844, GSE7451, and GSE40611 were downloaded from the Gene Expression Omnibus (GEO) database. The differentially expressed genes (DEGs) were identified with R software. Then, the DEGs were intersected with the immune genes obtained from the ImmPort database to acquire differentially expressed immune-related genes (DEIRGs), and functional enrichment analyses were performed. The DEIRGs were screened through the least absolute shrinkage and selection operator (LASSO) logistic regression algorithm to obtain the optimal immune-related genes (IRGs). Expression levels of the optimal IRGs were verified by quantitative reverse transcription-polymerase chain reaction (qRT-PCR) to obtain the key genes. Next, gene chips GSE7451 and GSE40611, from other tissues, were selected as the training sets to verify the sensitivity and specificity of the diagnosis of the key genes by receiver operating characteristic (ROC) analysis. RESULTS: A total of 54 DEIRGs were obtained. The functional enrichment analysis results showed that they play an important role in immune and inflammatory responses. Nine optimal IRGs were screened from the DEIRGs by the LASSO logistic regression algorithm. After qRT-PCR verification, eight out of nine optimal IRGs (, and ) were significantly highly expressed in pSS patients and were defined as key genes. ROC analysis identified that and had high sensitivity and specificity. Finally, the lack of previous research on and in pSS suggests that these IRGs may be regarded as new gateways to explore the diagnosis and pathogenesis of pSS. CONCLUSIONS: The key DEIRGs play a decisive role during the occurrence and development of pSS.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58d3/9096389/038387ffcb6a/atm-10-08-487-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58d3/9096389/47cec3739463/atm-10-08-487-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58d3/9096389/c5e5db9d1bbb/atm-10-08-487-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58d3/9096389/b4c94e3b12ab/atm-10-08-487-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58d3/9096389/928de9e6007e/atm-10-08-487-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58d3/9096389/5b57c8cdea73/atm-10-08-487-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58d3/9096389/d052a8e5f459/atm-10-08-487-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58d3/9096389/038387ffcb6a/atm-10-08-487-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58d3/9096389/47cec3739463/atm-10-08-487-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58d3/9096389/c5e5db9d1bbb/atm-10-08-487-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58d3/9096389/b4c94e3b12ab/atm-10-08-487-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58d3/9096389/928de9e6007e/atm-10-08-487-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58d3/9096389/5b57c8cdea73/atm-10-08-487-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58d3/9096389/d052a8e5f459/atm-10-08-487-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58d3/9096389/038387ffcb6a/atm-10-08-487-f7.jpg

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引用本文的文献

[1]
Expression of interleukin-18 in primary Sjögren syndrome and its potential mechanisms with disease: A systematic review and meta-analysis.

Medicine (Baltimore). 2025-3-21

[2]
Identification and verification of inflammatory biomarkers for primary Sjögren's syndrome.

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[3]
Associations between TNFSF13B polymorphisms and primary Sjögren's syndrome susceptibility in primary Sjögren's syndrome patients: A meta-analysis.

Immun Inflamm Dis. 2023-12

[4]
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Med Oral Patol Oral Cir Bucal. 2024-3-1

[5]
PSMC6 induces immune cell infiltration and inflammatory response to aggravate primary Sjögren's syndrome.

J Hum Genet. 2023-4

本文引用的文献

[1]
Integrated Bioinformatics and Validation Reveal Potential Biomarkers Associated With Progression of Primary Sjögren's Syndrome.

Front Immunol. 2021

[2]
A new molecular classification to drive precision treatment strategies in primary Sjögren's syndrome.

Nat Commun. 2021-6-10

[3]
Identification of key immune-related genes and immune infiltration in atrial fibrillation with valvular heart disease based on bioinformatics analysis.

J Thorac Dis. 2021-3

[4]
Activation of Toll-Like Receptor 7 Signaling Pathway in Primary Sjögren's Syndrome-Associated Thrombocytopenia.

Front Immunol. 2021

[5]
Montelukast alleviates inflammation in experimental autoimmune encephalomyelitis by altering Th17 differentiation in a mouse model.

Immunology. 2021-6

[6]
The Jak/STAT pathway: A focus on pain in rheumatoid arthritis.

Semin Arthritis Rheum. 2021-2

[7]
Transcriptome Sequencing Reveals Potential Roles of in Primary Sjögren's Syndrome.

Front Cell Dev Biol. 2020-12-4

[8]
LncRNA and mRNA expression profile of peripheral blood mononuclear cells in primary Sjögren's syndrome patients.

Sci Rep. 2020-11-12

[9]
Identification of a Prognostic Model Based on Immune-Related Genes of Lung Squamous Cell Carcinoma.

Front Oncol. 2020-9-2

[10]
Identification of hub genes in colon cancer via bioinformatics analysis.

J Int Med Res. 2020-9

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