Fig 1.
Flow chart of this study.
Fig 2.
Screening differentially expressed genes (DEGs) and senescence related DEGs in diabetic foot ulcer (DFU).
(A)The principal component analysis (PCA) displaying a distinct profile between GSE134431 and GSE199939. (B) The volcano plot showing upregulated (Red) and downregulated (Blue) DEGs. (C) Clustering analysis and heatmap of the DEGs between DFU and control groups.
Fig 3.
GO and KEGG Enrichment Analysis of DFU.
(A-C) The bubble plots of the GO enrichment of DEGs, including biological process, cellular component, and molecular function. (D) The Sankey diagram showing the KEGG enrichment analysis of DEGs.
Fig 4.
Identification of gene modules associated with DFU using WGCNA.
(A) The selection of optimal soft thresholding power. (B) Gene dendrogram and modules. Gene modules associated with DFU were shown in different colors under the gene dendrogram. (C) The correlation heatmap representing the relationship between different gene modules and status of DFU. (D-E) Scatter plots showing the correlation between module membership (MM) and gene significance (GS) in the red and brown modules. WGCNA, weighted gene co-expression network analysis.
Fig 5.
Construction of RF, SVM, KNN, NNET, LASSO and DT machine models.
(A) Intersection of the differentially expressed genes and immune-related genes. (B) The cumulative residual distribution of the six models. (C) Residual Boxplots of the six machine learning models, where the red dots indicate the root mean square of the residuals. (D) ROC analysis of six machine learning models with fivefold cross-validation in the test set. (E) The important features in RF, SVM, KNN, NNET, LASSO and DT.
Fig 6.
Validation analysis of machine learning of seven feature genes.
(A) Intersection of the three machine learning outcomes. (B) Gene expression boxplots for 7 feature genes. (C) ROC curve of 7 feature genes (The left is the training set and the right is the test set). (D) The diagnostic nomogram based on 7 feature genes. (E) Calibration curve to evaluate the accuracy of the nomogram(The left is the training set and the right is the test set). (F)ROC of the validation Gene Expression Omnibus (GEO) data set(The left is the training set and the right is the test set).(G) Decision curve of feature genes nomogram (The left is the training set and the right is the test set).
Fig 7.
Expression profiles of hub genes in single cells.
(A) Cellular subtypes of Diabetic foot ulcer. (B), (C) Scatter plots and bubble plot of the expression of the 7 hub genes.
Fig 8.
Single gene GSEA of characteristic genes.
GO and KEGG enrichment analysis using GSEA for the gene PI3 and S100A8, including enriched in high expression group and low expression group.
Fig 9.
Immune cell infiltration analysis.
(A) The stacked bar plot representing the different immune cell proportions in each sample. (B) The heatmap showing the correlation between different immune cells. Red represented a positive correlation, while blue represented a negative correlation. (C) The boxplot depicting the comparison of 22 types of immune cells between DCM and control groups.
Fig 10.
The ranking of drugs in the CMap database and the drug molecular structure.
(A) Ranking and scoring of drugs in the CMap database. (B) The molecular structure of drugs.
Fig 11.
(A) Binding energy results of molecular docking. (B) Presentation of molecular docking results.
Fig 12.
The molecular dynamics (MD) simulation of the PLA2G2A and naftopidil complex, PLA2G2A and PP-30 complex and FGFR3 and AZD-8055 complex.
(A) The RMSD plot of the PLA2G2A and naftopidil complex, PLA2G2A and PP-30 complex and FGFR3 and AZD-8055 complex. (B) The Rg plot of the PLA2G2A and naftopidil complex, PLA2G2A and PP-30 complex and FGFR3 and AZD-8055 complex. (C) The RMSF plot of the PLA2G2A and naftopidil complex, PLA2G2A and PP-30 complex and FGFR3 and AZD-8055 complex. (D) The number of hydrogen bonds in the PLA2G2A and naftopidil complex, PLA2G2A and PP-30 complex and FGFR3 and AZD-8055 complex.