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pmid:40487403
Identification of biomarkers and potential drug targets in DFU based on fundamental experiments and multi-omics joint analysis.
Xudong Xin · Haidong Zhou · Song Huang · Wenzhao Zhang · Jiahou Xu · Wei Wang · Jihua Wei · Liqing Li
Frontiers in pharmacology · 2025 doi:10.3389/fphar.2025.1561179
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Experiment
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Data
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Analysis
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Complete file
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The single-cell data were subjected to processing, annotation, differential gene expression analysis, and staining. The transcriptome sequencing data were analyzed using weighted gene co-expression network analysis (WGCNA), followed by assessment of immune infiltration. By integrating transcriptomic data and differentially expressed genes identified through WGCNA, co-expressed differentially expressed genes were obtained, and a protein-protein interaction (PPI) network was constructed followed by enrichment analysis. Core genes were screened using four machine learning models (Random Forest, Lasso, XGBoost, and SVM). Drug prediction was performed to identify potential therapeutic agents, and molecular docking simulations were conducted to assess the binding interactions between the macromolecular proteins encoded by the core genes and quercetin. A rat model of diabetic foot ulcer (DFU) was established and randomly divided into three groups: control, model, and treatment groups. Tissue samples were collected at 3, 7, and 14 days post-intervention for RT-qPCR, hematoxylin and eosin (H&E) staining, Masson's trichrome staining, and immunofluorescence staining to evaluate the therapeutic effects of quercetin via modulation of the core genes on DFU.\nResults: The analysis identified 275 differentially co-expressed genes that are extensively involved in the IL-17 signaling pathway, metabolic pathways, the PI3K/Akt signaling pathway, Staphylococcus aureus infection, complement and coagulation cascades, among others. From these, four core genes (CIB2, SAMHD1, DPYSL2, IFI44) were selected using machine learning techniques. Immune infiltration analysis demonstrated a strong correlation between SAMHD1, IFI44, DPYSL2, and macrophages. Molecular docking studies revealed that quercetin exhibits a lower binding energy with the target protein binding site, forming a stable structure. Single-cell analysis indicated that SAMHD1 is predominantly expressed in macrophages, whereas DPYSL2 is expressed not only in macrophages but also significantly in vascular endothelial cells and other cell types. This suggests that SAMHD1 and DPYSL2 may exert their effects by modulating these cells, as corroborated by basic experimental findings. The improvement in wound tissue morphology observed in the treatment group was more favorable compared to the model group. In comparison to the acute group, the gene expression profile in the model group aligned with bioinformatics predictions. Furthermore, the alterations in core gene expression following quercetin treatment were statistically significant.\nConclusion: Quercetin may enhance the healing of diabetic foot ulcers by modulating macrophage activity through the regulation of SAMHD1 and DPYSL2, thereby contributing to the recovery process.", "claims": [{"id": "claim-method", "statement": "Statistical analyses were conducted using SPSS version 26.0 to represent measurement data and to compare multiple samples through one-way analysis of variance (ANOVA). Based on the results of the homogeneity of variance test, the Least Significant Difference (LSD) method was employed when variances were equal, while the Tamhane’s T2 method was utilized in cases of unequal variances. 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A rat model of diabetic foot ulcer (DFU) was estab", "nvironment, 30 SPF-grade Sprague-Dawley male rats were randomly allocated into three groups: an acu", "stablish a rat model of type 1 diabetes, the rats were fasted for 12 h with unrestricted access to", "to water. On the day of model induction, the rats were weighed, and blood samples were collected fr"], "order_basis": "paper_text_order:1336", "id": "assay:1"}, {"role": "data_generation", "definition_id": "qpcr", "definition_version": "99e1195c7d6f", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"assay_lexicon": "99e1195c7d6f"}, "confidence": 0.99, "evidence": ["d at 3, 7, and 14 days post-intervention for RT-qPCR, hematoxylin and eosin (H&E) staining, Masso", "t 3, 7, and 14 days post-intervention for RT-qPCR, hematoxylin and eosin (H&E) staining, Masso", "AMHD1 were subsequently quantified using the RT-qPCR method. A fluorescent quantitative PCR instr", "odel. 2.2.2.6 Real-time quantitative PCR (RT qPCR) method Total RNA was extracted from tissue"], "order_basis": "paper_text_order:1542", "id": "assay:2"}, {"role": "data_generation", "definition_id": "ihc", "definition_version": "99e1195c7d6f", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"assay_lexicon": "99e1195c7d6f"}, "confidence": 0.93, "evidence": [") staining, Masson's trichrome staining, and immunofluorescence staining to evaluate the therapeutic effects"], "order_basis": "paper_text_order:1622", "id": "assay:3"}, {"role": "analysis", "definition_id": "group_comparison", "definition_version": "f2132e96ae6c7a4e", "definition_digest": null, "required_operations": ["group_summary", "welch_t", "bootstrap_mean_difference", "group_comparison_anova"], "support_state": "supported", "source_hashes": {"dsl_catalogue": "f2132e96ae6c7a4e"}, "confidence": 1.0, "evidence": ["Statistical analyses were conducted using SPSS version 26.0 to represent measurement data and to compare multiple samples through one-way analysis of variance (ANOVA). 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