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Updated: Jul 29, 2026
Analyses of Proteinuria, Renal Infiltration of Leukocytes, and Renal Deposition of Proteins in Lupus-prone MRL/lpr Mice
Published on: June 8, 2022
Comprehensive Analysis of Ferroptosis Markers in Lupus Nephritis Based on Bioinformatics Analysis and Experimental
Su Zhang1,2, Weitao Hu3, Chunyan Huang4
1The Second Clinical College of Fujian Medical University, Quanzhou, People's Republic of China.
Introduction:
Lupus nephritis (LN) is a common and severe complication of systemic lupus erythematosus (SLE). Ferroptosis is a form of iron-dependent cell death induced by lipid peroxidation. However, its specific role in LN remains unclear.
Methods:
We utilized the GSE32591 obtained from the GEO database to identify differentially expressed genes (DEGs) and conduct enrichment analysis. Differentially expressed ferroptosis-related genes of LN (LNDE-FRGs) were derived by taking the intersection of DEGs and ferroptosis-related genes (FRGs). Three machine learning algorithms were applied to screen candidate key LNDE-FRGs. The expression of the key LNDE-FRGs was validated using external validation cohorts and clinical samples. The diagnostic value of the key LNDE-FRGs was then assessed by receiver operating characteristic curve (ROC) analysis. In addition, we investigated the correlation between the key genes and glomerular filtration rate (GFR), urinary protein and serum creatinine (Scr) in LN patients via the Nephroseq V5 database. Subsequently, we performed immune infiltrating cell analysis of LN kidney tissue using Cibersort. Finally, we validated the expression of the key gene CYBB by clinical samples and in vivo experiments.
Results:
A total of 377 DEGs and 20 LNDE-FRGs were identified. Machine learning algorithms selected four candidate key LNDE-FRGs (CD44, CYBB, TCF4, and PARP12). However, only CYBB exhibited consistent expression trends in both the training and validation cohorts (P < 0.05). Immune infiltration analysis revealed that the expression levels of monocytes and M0 macrophages were significantly higher in the LN group than in the normal control group. In addition, there was a correlation between key genes and GFR, urinary protein and Scr. Finally, the expression level of CYBB was verified in lupus mice.
Conclusion:
CYBB may be a ferroptosis-related biomarker in LN. This may provide new ideas for the clinical treatment and pathogenesis of LN.
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