Lumican as a potential biomarker for diabetic nephropathy.

IF 3 3区 医学 Q1 UROLOGY & NEPHROLOGY Renal Failure Pub Date : 2025-12-01 Epub Date: 2025-04-07 DOI:10.1080/0886022X.2025.2480245
Yuejia Tao, Yipeng Liu, Zunsong Wang, Lijun Tang, Ying Zhang, Shanshan Zheng, Ruixue Wang, Kai Wei, Shunyao Liu
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Abstract

Objective: We employed bioinformatics to identify potential biomarkers for diabetic nephropathy (DN) and investigate the role of the key gene lumican in its molecular processes.

Methods: We analyzed the GSE96804 and GSE30528 DN datasets from the Gene Expression Omnibus (GEO). GO and GSEA-KEGG enrichment analyses were used to identify key biological functions and related pathways. Cytoscape software was used to screen differentially expressed genes (DEGs) to obtain hub genes. The Nephroseq database was used to analyze the effect of hub genes on renal function, and the importance of lumican, a gene potentially related to DN progression, was further examined in clinical samples. GO and KEGG analyses were performed on lumican and its interacting proteins to elucidate their main biological functions and related pathways.

Results: We identified 1139 DEGs. GO enrichment analysis revealed that the DEGs were mainly involved in responses to hexose, cell-cell junctions. GSEA-KEGG enrichment analysis indicated that the DEGs were related to amino acid metabolism, adipokine signaling. Nephroseq database analysis revealed that hub genes were upregulated in the kidney tissues of patients with DN and that their expression was negatively correlated with estimated glomerular filtration rate (eGFR). Lumican was among the top hub genes, and its expression was increased in renal tissues of DN patients as confirmed by immunohistochemistry and immunofluorescence. GO and KEGG enrichment analyses revealed that lumican and its interacting proteins were associated with extracellular matrix organization.

Conclusion: Lumican is a potential biomarker for predicting DN and is closely related to the extracellular matrix. These findings provide novel insights into the clinical diagnosis and treatment of DN.

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Lumican作为糖尿病肾病的潜在生物标志物。
目的:利用生物信息学方法鉴定糖尿病肾病(DN)的潜在生物标志物,并探讨关键基因lumican在其分子过程中的作用。方法:分析来自GEO的GSE96804和GSE30528 DN数据集。GO和GSEA-KEGG富集分析用于鉴定关键的生物学功能和相关途径。使用Cytoscape软件筛选差异表达基因(DEGs),获得中心基因。使用Nephroseq数据库分析hub基因对肾功能的影响,并在临床样本中进一步检查与DN进展可能相关的基因lumican的重要性。对lumican及其相互作用蛋白进行GO和KEGG分析,以阐明其主要生物学功能和相关途径。结果:鉴定出1139个deg。氧化石墨烯富集分析显示,deg主要参与对己糖、细胞-细胞连接的反应。GSEA-KEGG富集分析表明,deg与氨基酸代谢、脂肪因子信号传导有关。Nephroseq数据库分析显示,hub基因在DN患者的肾脏组织中表达上调,其表达与估计的肾小球滤过率(eGFR)呈负相关。Lumican是顶级枢纽基因之一,免疫组化和免疫荧光证实其在DN患者肾组织中的表达升高。GO和KEGG富集分析显示,lumican及其相互作用蛋白与细胞外基质组织有关。结论:Lumican与细胞外基质密切相关,是一种潜在的预测DN的生物标志物。这些发现为DN的临床诊断和治疗提供了新的见解。
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来源期刊
Renal Failure
Renal Failure 医学-泌尿学与肾脏学
CiteScore
3.90
自引率
13.30%
发文量
374
审稿时长
1 months
期刊介绍: Renal Failure primarily concentrates on acute renal injury and its consequence, but also addresses advances in the fields of chronic renal failure, hypertension, and renal transplantation. Bringing together both clinical and experimental aspects of renal failure, this publication presents timely, practical information on pathology and pathophysiology of acute renal failure; nephrotoxicity of drugs and other substances; prevention, treatment, and therapy of renal failure; renal failure in association with transplantation, hypertension, and diabetes mellitus.
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