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pmid:41255601
Identification of anoikis-related genes and immune infiltration characteristics in Sjögren's syndrome based on machine learning.
Lei Wang · Ziqi Zhou · Xinpeng Zhou · Ying Liu · Mengjie Wang
Frontiers in medicine · 2025 doi:10.3389/fmed.2025.1661259
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Experiment
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Data
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Complete file
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Although accumulating evidence indicates its involvement in modulating immune responses and contributing to SS progression, the precise role of anoikis in SS remains inadequately understood. This study aimed to explore anoikis-related genes (ARGs) and their molecular mechanisms in SS using public databases.\nMethods: SS datasets (GSE23117, GSE84844 and GSE12795) were retrieved from the GEO database. In total, 924 ARGs were extracted from the GeneCards and Harmonizome databases, followed by differential expression gene (DEGs) analysis and weighted gene co-expression network analysis (WGCNA). Machine learning algorithms were utilized to screen candidate biomarkers, and their diagnostic effectiveness was assessed using receiver operating characteristic (ROC) curve analysis. Concurrently, a mouse model of SS was established and validated through in vivo experiments. Immune cell infiltration in SS tissues was evaluated using CIBERSORT, and correlations between characteristic genes and immune cell profiles were analyzed. Potential drug candidates targeting these genes were identified using the DGIdb database. Subsequently, an lncRNA-miRNA-mRNA network associated with these genes was constructed, and preliminary experimental validation was conducted.\nResults: A total of 35 differentially expressed anoikis-related genes (DEARGs) were identified. GO and KEGG enrichment analyses demonstrated that DEARGs were primarily associated with inflammation, viral infections, and the necroptosis signaling pathway. Machine learning analysis pinpointed 14 feature genes, among seven were associated with cancer (NAT1, BIRC3, EZH2, MAD2L1, ATP2A3, HMGA1, and BST2). Given the unclear roles of SKI and PRDX4 in SS, the study focused specifically on five relevant genes, MAPK3, IL15, S100A9, IFI27, and CXCL10, which were validated by in vivo experiments. Immune cell analysis revealed increased proportions of B cells, T cells, macrophages, and other immune cells in SS tissues. Furthermore, ceRNA and drug-gene interaction networks were established, underscoring the regulatory significance of five key miRNAs (miR-30b-5p, miR-148a-3p, miR-130a, miR-483-5p, and miR-486-3p) in SS. In addition, eight candidate drugs were identified with potential for modulating SS pathogenesis.\nConclusion: This study substantiates the significant involvement of anoikis in SS and suggests that MAPK3, IL15, S100A9, IFI27, and CXCL10 may serve as critical biomarkers in the inflammatory progression of SS. These genes likely mediate their effects by influencing immune cell infiltration, participating in immune regulation, and modulating inflammatory responses. Our findings offer new insights into drug selection and immunotherapeutic strategies for SS.", "claims": [{"id": "claim-method", "statement": "The “limma” package in R facilitated the analysis of DEGs in the GSE23117 and GSE84844 datasets.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:41255601", "locator": "sections[4] \"Identification of differentially expressed genes\" paragraph 2", "quote": "The “limma” package in R facilitated the analysis of DEGs in the GSE23117 and GSE84844 datasets."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The original contributions presented in the study are included in the article/Supplementary material, further inquiries can be directed to the corresponding author/s.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:41255601", "locator": "sections[31] \"Data availability statement\" paragraph 2", "quote": "The original contributions presented in the study are included in the article/Supplementary material, further inquiries can be directed to the corresponding author/s."}], "state": "complete"}, {"id": "claim-target-result", "statement": "Using the limma package with expression data retrieved from GEO, the study identified 559 differentially expressed genes and 35 differentially expressed anoikis-related genes in Sjögren’s syndrome.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:41255601", "locator": "sections[19] \"Differential expression analysis and identification of ARGs in SS\" paragraph 2", "quote": "Using the limma package, 559 DEGs were identified in the SS datasets, including 434 upregulated and 125 downregulated genes (Figure 2C)."}, {"asset": "source:pmid:41255601", "locator": "sections[19] \"Differential expression analysis and identification of ARGs in SS\" paragraph 2", "quote": "Among the 924 ARGs obtained from the GeneCards and Harmonizome databases, 35 DEARGs were obtained through intersection with the identified DEGs (Figures 2D,E)."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "partial", "objective": "Using the limma package with expression data retrieved from GEO, the study identified 559 differentially expressed genes and 35 differentially expressed anoikis-related genes in Sjögren’s syndrome.", "steps": [{"id": "read_published_estimate", "order": 1, "name": "Read the published estimate from the source", "kind": "other", "state": "complete", "blocked_on": null, "description": "The claim, method and evidence span published with the source article.", "duration_hours": null, "parameters": {}, "inputs": ["source:pmid:41255601"], "outputs": ["the published estimate and its evidence"], "instruments": [], "reagents": []}, {"id": "obtain_source_data", "order": 2, "name": "Obtain the source data from the named repository", "kind": "data-preparation", "state": "blocked", "blocked_on": "data:accession_absent", "description": "The GEO series accession resolves and its sample accessions are listed. 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