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pmid:40162084

Analysis and Validation of Mitophagy-Related Genes in Diabetic Foot Ulcers.

Shaoyihan Fang · Huijuan Zhang · Wenjian Liu · Shuangyan Li · Zhenzhen Chen · Jingjie Min · Chengyu Dai · Jingwen An · Hongxiao Zhang · Dewu Liu

Journal of inflammation research · 2025 doi:10.2147/JIR.S504001

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:40162084
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science-record
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sha256:cdce0a65cfa024c17730cebd998c1535b90f064eb7075d94d9d7032e3f2bf679
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https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json
created_at
2026-11-01T20:30:21Z
updated_at
2026-11-01T22:56:18Z
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paper object · 10 fields
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complete
title
Analysis and Validation of Mitophagy-Related Genes in Diabetic Foot Ulcers.
doi
10.2147/JIR.S504001
pmid
40162084
authors array · 10 items
[0]
Shaoyihan Fang
[1]
Huijuan Zhang
[2]
Wenjian Liu
[3]
Shuangyan Li
[4]
Zhenzhen Chen
[5]
Jingjie Min
[6]
Chengyu Dai
[7]
Jingwen An
[8]
Hongxiao Zhang
[9]
Dewu Liu
journal
Journal of inflammation research
year
2025
abstract
Purpose: This study aimed to identify hub genes associated with mitophagy involved in the pathogenesis and progression of diabetic foot ulcer (DFU), and to characterize their immune cell infiltration features and single-cell expression profiles. Methods: DFU-related datasets (GSE80178, GSE68183) were retrieved from the GEO database. Subsequently, differentially expressed genes (DEGs) were identified via limma analysis, followed by gene set enrichment analysis (GSEA) to assess gene function enrichment. Identified DEGs were intersected with mitophagy-related genes. Machine learning (ML) algorithms were further employed to identify hub genes. Additionally, immune cell infiltration was examined via the CIBERSORT algorithm, and the correlation between the identified genes and immune infiltration was investigated. Finally, hub genes identified were validated via the single-cell RNA sequencing dataset GSE165816, and further validated using RT-PCR and Western blot (WB) assays. Results: Two hub genes, ANO6 and ALDH2, were identified and found to be significantly downregulated in the skin tissues of patients with DFU. Receiver operating characteristic (ROC) analysis demonstrated robust diagnostic potential (ANO6, AUC = 0.833, ALDH2, AUC = 0.806). Immune cell infiltration analysis demonstrated notable differences between the DFU and normal groups in naïve B cells, monocytes, resting mast cells, γδT cells, and regulatory T cells (Tregs). The findings were further validated through single-cell RNA sequencing (scRNA-seq) analysis and experimental studies, which confirmed the downregulation of ANO6 and ALDH2 in DFU tissues. Conclusion: Two mitophagy-related hub genes, ANO6 and ALDH2, were identified and validated as being significantly downregulated in DFU. Both genes demonstrated diagnostic potential and showed an association with immune cell infiltration. These findings suggest that mitophagy dysfunction may contribute to the pathophysiology of DFU, potentially through the dysregulation of inflammatory pathways and immune responses. While the results provide valuable insights into DFU and its management, further studies with larger cohorts and deeper exploration of mechanistic links to inflammation are necessary to translate these findings into therapeutic strategies.
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Two ML methods were employed to screen for hub genes in this study.
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sections[5] "Identification of Hub Genes" paragraph 2
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Two ML methods were employed to screen for hub genes in this study.
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RNA sequencing data were acquired from DFU and normal tissue samples (GSE80178, GSE68183) sourced from human subjects. The GSE80178 dataset comprised 3 normal tissue samples and 9 DFU tissue samples, whereas GSE68183 contained 3 normal skin tissue samples and 3 DFU tissue samples.
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sections[3] "Microarray Data Collection" paragraph 2
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RNA sequencing data were acquired from DFU and normal tissue samples (GSE80178, GSE68183) sourced from human subjects. The GSE80178 dataset comprised 3 normal tissue samples and 9 DFU tissue samples, whereas GSE68183 contained 3 normal skin tissue samples and 3 DFU tissue samples.
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Two mitophagy-related hub genes, ANO6 and ALDH2, were identified and validated as being significantly downregulated in DFU.
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Two mitophagy-related hub genes, ANO6 and ALDH2, were identified and validated as being significantly downregulated in DFU.
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Two mitophagy-related hub genes, ANO6 and ALDH2, were identified and validated as being significantly downregulated in DFU.
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Single Cell Transcriptomic Landscape of Diabetic Foot Ulcers
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Comparative genomic, microRNA, and tissue analyses reveal subtle differences between non-diabetic and diabetic foot skin [gene expression]
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Genomic Profiling of Diabetic Foot Ulcers Identifies miR-15b-5p as a Major Regulator that Leads to Suboptimal Inflammatory Response and Diminished DNA Repair Mechanisms
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hub genes identified were validated via the single-cell RNA sequencing dataset GSE165816, and further validated usi
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alidated through single-cell RNA sequencing (scRNA-seq) analysis and experimental studies, which co
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[0]
Two ML methods were employed to screen for hub genes in this study.
order_basis
consumes_earlier_output
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assay:4
Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:40162084", "kind": "science-record", "revision": 4, "content_hash": "sha256:cdce0a65cfa024c17730cebd998c1535b90f064eb7075d94d9d7032e3f2bf679", "created_at": "2026-11-01T20:30:21Z", "updated_at": "2026-11-01T22:56:18Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Analysis and Validation of Mitophagy-Related Genes in Diabetic Foot Ulcers.", "doi": "10.2147/JIR.S504001", "pmid": "40162084", "authors": ["Shaoyihan Fang", "Huijuan Zhang", "Wenjian Liu", "Shuangyan Li", "Zhenzhen Chen", "Jingjie Min", "Chengyu Dai", "Jingwen An", "Hongxiao Zhang", "Dewu Liu"], "journal": "Journal of inflammation research", "year": 2025, "abstract": "Purpose: This study aimed to identify hub genes associated with mitophagy involved in the pathogenesis and progression of diabetic foot ulcer (DFU), and to characterize their immune cell infiltration features and single-cell expression profiles.\nMethods: DFU-related datasets (GSE80178, GSE68183) were retrieved from the GEO database. Subsequently, differentially expressed genes (DEGs) were identified via limma analysis, followed by gene set enrichment analysis (GSEA) to assess gene function enrichment. Identified DEGs were intersected with mitophagy-related genes. Machine learning (ML) algorithms were further employed to identify hub genes. Additionally, immune cell infiltration was examined via the CIBERSORT algorithm, and the correlation between the identified genes and immune infiltration was investigated. Finally, hub genes identified were validated via the single-cell RNA sequencing dataset GSE165816, and further validated using RT-PCR and Western blot (WB) assays.\nResults: Two hub genes, ANO6 and ALDH2, were identified and found to be significantly downregulated in the skin tissues of patients with DFU. Receiver operating characteristic (ROC) analysis demonstrated robust diagnostic potential (ANO6, AUC = 0.833, ALDH2, AUC = 0.806). Immune cell infiltration analysis demonstrated notable differences between the DFU and normal groups in naïve B cells, monocytes, resting mast cells, γδT cells, and regulatory T cells (Tregs). The findings were further validated through single-cell RNA sequencing (scRNA-seq) analysis and experimental studies, which confirmed the downregulation of ANO6 and ALDH2 in DFU tissues.\nConclusion: Two mitophagy-related hub genes, ANO6 and ALDH2, were identified and validated as being significantly downregulated in DFU. Both genes demonstrated diagnostic potential and showed an association with immune cell infiltration. These findings suggest that mitophagy dysfunction may contribute to the pathophysiology of DFU, potentially through the dysregulation of inflammatory pathways and immune responses. While the results provide valuable insights into DFU and its management, further studies with larger cohorts and deeper exploration of mechanistic links to inflammation are necessary to translate these findings into therapeutic strategies.", "claims": [{"id": "claim-method", "statement": "Two ML methods were employed to screen for hub genes in this study.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:40162084", "locator": "sections[5] \"Identification of Hub Genes\" paragraph 2", "quote": "Two ML methods were employed to screen for hub genes in this study."}], "state": "complete"}, {"id": "claim-data-access", "statement": "RNA sequencing data were acquired from DFU and normal tissue samples (GSE80178, GSE68183) sourced from human subjects. 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This lane did not download the dataset or read its licence.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE165816"], "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:machine_learning_random_forest", "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:GSE165816"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": ["step:run_analysis blocked on method:machine_learning_random_forest"]}, "data": {"state": "partial", "assets": [{"id": "source:pmid:40162084", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.2147/JIR.S504001", "sha256": "sha256:55655903182fcb186f2614905570fc24bf939b81c7dfe20abbe3ec678fc38742", "bytes": 42655, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.2147/JIR.S504001", "version": null, "note": "Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.", "structure": {"pmcid": "PMC11954483", "source": "europe_pmc_fulltext", "coverage": "whole_body", "text_hash_scope": "rendered_section_body"}}, {"id": "data:geo:GSE165816", "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=GSE165816", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE165816", "version": null, "note": "RNA sequencing data were acquired from DFU and normal tissue samples (GSE80178, GSE68183) sourced from human subjects. 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