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pmid:39697326

Integrative analysis of PANoptosis-related genes in diabetic retinopathy: machine learning identification and experimental validation.

Han Chen · Enguang Chen · Ting Cao · Feifan Feng · Min Lin · Xuan Wang · Yu Xu

Frontiers in immunology · 2024 doi:10.3389/fimmu.2024.1486251

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pmid:39697326
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title
Integrative analysis of PANoptosis-related genes in diabetic retinopathy: machine learning identification and experimental validation.
doi
10.3389/fimmu.2024.1486251
pmid
39697326
authors array · 7 items
[0]
Han Chen
[1]
Enguang Chen
[2]
Ting Cao
[3]
Feifan Feng
[4]
Min Lin
[5]
Xuan Wang
[6]
Yu Xu
journal
Frontiers in immunology
year
2024
abstract
Background: Diabetic retinopathy (DR) is a major complication of diabetes, leading to severe vision impairment. Understanding the molecular mechanisms, particularly PANoptosis, underlying DR is crucial for identifying potential biomarkers and therapeutic targets. This study aims to identify differentially expressed PANoptosis-related genes (DE-PRGs) in DR, offering insights into the disease's pathogenesis and potential diagnostic tools. Methods: DR datasets were obtained from the Gene Expression Omnibus (GEO) database, while PANoptosis-related genes were sourced from the GeneCards database. Differentially expressed genes (DEGs) were identified using the DESeq2 package, followed by functional enrichment analysis through DAVID and Metascape tools. Three machine learning algorithms-LASSO regression, Random Forest, and SVM-RFE-were employed to identify hub genes. A diagnostic nomogram was constructed and its performance assessed via ROC analysis. The CIBERSORT algorithm analyzed immune cell infiltration. Hub genes were validated through RT-qPCR, Western blotting, immunohistochemistry, and publicly available datasets. Additionally, the impact of FASN and PLSCR3 knockdown on HUVECs behavior was validated through in vitro experiments. Results: Differential expression analysis identified 1,418 DEGs in the GSE221521 dataset, with 39 overlapping DE-PRGs (29 upregulated, 10 downregulated). Functional enrichment indicated that DE-PRGs are involved in apoptosis, signal transduction, and inflammatory responses, with key pathways such as MAPK and TNF signaling. Machine learning algorithms identified six PANoptosis-related hub genes (BEX2, CASP2, CD36, FASN, OSMR, and PLSCR3) as potential biomarkers. A diagnostic nomogram based on these hub genes showed high diagnostic accuracy. Immune cell infiltration analysis revealed significant differences in immune cell patterns between control and DR groups, especially in Activated CD4 Memory T Cells and Monocytes. Validation confirmed the diagnostic efficiency and expression patterns of the PANoptosis-related hub genes, supported by in vitro and the GSE60436 dataset analysis. Furthermore, experiments demonstrated that knocking down FASN and PLSCR3 impacted HUVECs behavior. Conclusion: This study provides valuable insights into the molecular mechanisms of DR, particularly highlighting PANoptosis-related pathways, and identifies potential biomarkers and therapeutic targets for the disease.
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sections[4] "Identification of differentially expressed PANoptosis-related genes" paragraph 2
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For the GSE221521 dataset, the DESeq2 package was used to normalize raw read counts and identify DEGs by comparing DR samples with healthy controls (14).
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The original contributions presented in the study are included in the article/ Supplementary Material . Further inquiries can be directed to the corresponding author.
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Differential expression analysis identified 1,418 DEGs in the GSE221521 dataset, with 39 overlapping DE-PRGs (29 upregulated, 10 downregulated).
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Differential expression analysis identified 1,418 DEGs in the GSE221521 dataset, with 39 overlapping DE-PRGs (29 upregulated, 10 downregulated).
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Differential expression analysis identified 1,418 DEGs in the GSE221521 dataset, with 39 overlapping DE-PRGs (29 upregulated, 10 downregulated).
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filtration. Hub genes were validated through RT-qPCR, Western blotting, immunohistochemistry, and
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tration. Hub genes were validated through RT-qPCR, Western blotting, immunohistochemistry, and
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n. Hub genes were validated through RT-qPCR, Western blotting, immunohistochemistry, and publicly availabl
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validated through RT-qPCR, Western blotting, immunohistochemistry, and publicly available datasets. Additional
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Additionally, the impact of FASN and PLSCR3 knockdown on HUVECs behavior was validated through in
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hment indicated that DE-PRGs are involved in apoptosis, signal transduction, and inflammatory respo
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_SIGNALING”. Additionally, we observed that “APOPTOSIS” was significantly positively correlated wit
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Cat. CRL-1730) were purchased from ATCC and cultured in endothelial cell medium supplemented with 10
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For the GSE221521 dataset, the DESeq2 package was used to normalize raw read counts and identify DEGs by comparing DR samples with healthy controls (14).
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:39697326", "kind": "science-record", "revision": 4, "content_hash": "sha256:dc6fe7e1977d928d2cf076bbaffe27736a87d48997d51aeb8d6240e268ea68ed", "created_at": "2026-11-01T20:29:59Z", "updated_at": "2026-11-01T22:55:50Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Integrative analysis of PANoptosis-related genes in diabetic retinopathy: machine learning identification and experimental validation.", "doi": "10.3389/fimmu.2024.1486251", "pmid": "39697326", "authors": ["Han Chen", "Enguang Chen", "Ting Cao", "Feifan Feng", "Min Lin", "Xuan Wang", "Yu Xu"], "journal": "Frontiers in immunology", "year": 2024, "abstract": "Background: Diabetic retinopathy (DR) is a major complication of diabetes, leading to severe vision impairment. Understanding the molecular mechanisms, particularly PANoptosis, underlying DR is crucial for identifying potential biomarkers and therapeutic targets. This study aims to identify differentially expressed PANoptosis-related genes (DE-PRGs) in DR, offering insights into the disease's pathogenesis and potential diagnostic tools.\nMethods: DR datasets were obtained from the Gene Expression Omnibus (GEO) database, while PANoptosis-related genes were sourced from the GeneCards database. Differentially expressed genes (DEGs) were identified using the DESeq2 package, followed by functional enrichment analysis through DAVID and Metascape tools. Three machine learning algorithms-LASSO regression, Random Forest, and SVM-RFE-were employed to identify hub genes. A diagnostic nomogram was constructed and its performance assessed via ROC analysis. The CIBERSORT algorithm analyzed immune cell infiltration. Hub genes were validated through RT-qPCR, Western blotting, immunohistochemistry, and publicly available datasets. Additionally, the impact of FASN and PLSCR3 knockdown on HUVECs behavior was validated through in vitro experiments.\nResults: Differential expression analysis identified 1,418 DEGs in the GSE221521 dataset, with 39 overlapping DE-PRGs (29 upregulated, 10 downregulated). Functional enrichment indicated that DE-PRGs are involved in apoptosis, signal transduction, and inflammatory responses, with key pathways such as MAPK and TNF signaling. Machine learning algorithms identified six PANoptosis-related hub genes (BEX2, CASP2, CD36, FASN, OSMR, and PLSCR3) as potential biomarkers. A diagnostic nomogram based on these hub genes showed high diagnostic accuracy. Immune cell infiltration analysis revealed significant differences in immune cell patterns between control and DR groups, especially in Activated CD4 Memory T Cells and Monocytes. Validation confirmed the diagnostic efficiency and expression patterns of the PANoptosis-related hub genes, supported by in vitro and the GSE60436 dataset analysis. Furthermore, experiments demonstrated that knocking down FASN and PLSCR3 impacted HUVECs behavior.\nConclusion: This study provides valuable insights into the molecular mechanisms of DR, particularly highlighting PANoptosis-related pathways, and identifies potential biomarkers and therapeutic targets for the disease.", "claims": [{"id": "claim-method", "statement": "For the GSE221521 dataset, the DESeq2 package was used to normalize raw read counts and identify DEGs by comparing DR samples with healthy controls (14).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:39697326", "locator": "sections[4] \"Identification of differentially expressed PANoptosis-related genes\" paragraph 2", "quote": "For the GSE221521 dataset, the DESeq2 package was used to normalize raw read counts and identify DEGs by comparing DR samples with healthy controls (14)."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The original contributions presented in the study are included in the article/ Supplementary Material . 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This lane did not download the dataset or read its licence.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE221521"], "outputs": ["the source data with its repository provenance"], "instruments": [], "reagents": []}, {"id": "run_analysis", "order": 3, "name": "Run the published analysis", "kind": "analysis", "state": "complete", "blocked_on": null, "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:GSE221521"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:39697326", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.3389/fimmu.2024.1486251", "sha256": "sha256:79b30f537bb1511252fc0b5b64bb29b637205ea9a6ea26633c5ba21724241784", "bytes": 41249, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.3389/fimmu.2024.1486251", "version": null, "note": "Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.", "structure": {"pmcid": "PMC11652367", "source": "europe_pmc_fulltext", "coverage": "whole_body_without_references", "text_hash_scope": "rendered_section_body"}}, {"id": "data:geo:GSE221521", "role": "raw", "format": "geo-series", "media_type": "application/vnd.ncbi.geo-series+json", "uri": "https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE221521", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE221521", "version": null, "note": "The original contributions presented in the study are included in the article/ Supplementary Material . 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Hub genes were validated through RT-qPCR, Western blotting, immunohistochemistry, and", "tration. Hub genes were validated through RT-qPCR, Western blotting, immunohistochemistry, and"], "order_basis": "paper_text_order:1139", "id": "assay:1"}, {"role": "data_generation", "definition_id": "western_blot", "definition_version": "99e1195c7d6f", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"assay_lexicon": "99e1195c7d6f"}, "confidence": 0.93, "evidence": ["n. 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Additional"], "order_basis": "paper_text_order:1166", "id": "assay:3"}, {"role": "data_generation", "definition_id": "transfection", "definition_version": "99e1195c7d6f", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"assay_lexicon": "99e1195c7d6f"}, "confidence": 0.85, "evidence": ["Additionally, the impact of FASN and PLSCR3 knockdown on HUVECs behavior was validated through in"], "order_basis": "paper_text_order:1266", "id": "assay:4"}, {"role": "data_generation", "definition_id": "apoptosis_assay", "definition_version": "99e1195c7d6f", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"assay_lexicon": "99e1195c7d6f"}, "confidence": 0.93, "evidence": ["hment indicated that DE-PRGs are involved in apoptosis, signal transduction, and inflammatory respo", "_SIGNALING”. Additionally, we observed that “APOPTOSIS” was significantly positively correlated wit"], "order_basis": "paper_text_order:1553", "id": "assay:5"}, {"role": "data_generation", "definition_id": "cell_culture", "definition_version": "99e1195c7d6f", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"assay_lexicon": "99e1195c7d6f"}, "confidence": 0.99, "evidence": ["Cat. CRL-1730) were purchased from ATCC and cultured in endothelial cell medium supplemented with 10", "Cat. CRL-1730) were purchased from ATCC and cultured in endothelial cell medium supplemented with"], "order_basis": "paper_text_order:3072", "id": "assay:6"}, {"role": "analysis", "definition_id": "differential_expression", "definition_version": "f2132e96ae6c7a4e", "definition_digest": null, "required_operations": ["normalise_counts", "differential_expression_fit", "fdr_bh"], "support_state": "supported", "source_hashes": {"dsl_catalogue": "f2132e96ae6c7a4e"}, "confidence": 1.0, "evidence": ["For the GSE221521 dataset, the DESeq2 package was used to normalize raw read counts and identify DEGs by comparing DR samples with healthy controls (14)."], "order_basis": "consumes_earlier_output", "id": "assay:7"}]}