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Research of the association between albumin and mitophagy in autosomal dominant polycystic kidney disease based on bioinformatics analysis
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Sen-tao PAN1, 2, Zhi-wei QIU2, Yu CHEN1, 2, Qian XIANG2, Yi-min CUI1, 2
Chinese Journal of Clinical Pharmacology | 2026, 42(1) : 119 - 123
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Chinese Journal of Clinical Pharmacology | 2026, 42(1): 119-123
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Research of the association between albumin and mitophagy in autosomal dominant polycystic kidney disease based on bioinformatics analysis
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Sen-tao PAN1, 2, Zhi-wei QIU2, Yu CHEN1, 2, Qian XIANG2, Yi-min CUI1, 2
Affiliations
  • 1.School of Pharmacy, Wenzhou Medical University, Wenzhou 325035, Zhejiang Province, China
  • 2.Institute of Clinical Pharmacology, Peking University First Hospital, Beijing 100034, China
Published: 2026-01-17 doi: 10.13699/j.cnki.1001-6821.2026.01.019
Outline
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Objective

To investigate the potential mechanisms and related signaling pathways of mitophagy in the occurrence and development of autosomal dominant polycystic kidney disease (ADPKD) using bioinformatics techniques.

Methods

The gene expression omnibus (GEO) dataset GSE7869 was downloaded and processed. Differentially expressed genes (DEGs) were identified using the R limma package. Mitophagy-related genes were retrieved from the GeneCards database and intersected with the DEGs to obtain candidate genes. A protein-protein interaction (PPI) network was constructed using STRING, and core genes were identified in Cytoscape using the maximalclique centrality (MCC) algorithm. Gene set enrichment analysis (GSEA) was conducted based on albumin (ALB) expression levels, and R packages including clusterProfiler, ggplot2 and enrichplot were used to visualize and interpret the enrichment results.

Results

A total of 248 DEGs were obtained, including 61 up-regulated and 187 down-regulated genes. After intersecting with mitophagy-related genes, 38 candidate DEGs were identified. ALB was identified as the core differentially expressed gene through PPI analysis and Cytoscape. GSEA results indicated that the mitophagy-related gene ALB may play a role in ADPKD by regulating pathways such as extracellular matrix (ECM)-receptor interaction and branched-chain amino acid (BCAA) metabolism, as well as biological processes including organic acid and amino acid metabolism and organization of collagen fibrils.

Conclusions

ALB expression levels were significantly associated with pathways including ECM-receptor interaction and branched-chain amino acid metabolism, as well as with biological processes such as organic acid and amino acid metabolism and organization of collagen fibrils. These findings suggest that ALB may be involved in the pathogenesis of ADPKD.

mitophagy  /  autosomal dominant polycystic kidney disease  /  bioinformatics  /  mechanism
Sen-tao PAN, Zhi-wei QIU, Yu CHEN, Qian XIANG, Yi-min CUI. Research of the association between albumin and mitophagy in autosomal dominant polycystic kidney disease based on bioinformatics analysis[J]. Chinese Journal of Clinical Pharmacology, 2026 , 42 (1) : 119 -123 . DOI: 10.13699/j.cnki.1001-6821.2026.01.019
Year 2026 volume 42 Issue 1
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Article Info
doi: 10.13699/j.cnki.1001-6821.2026.01.019
  • Receive Date:2025-10-20
  • Online Date:2026-08-06
  • Published:2026-01-17
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History
  • Received:2025-10-20
Funding
Affiliations
    1.School of Pharmacy, Wenzhou Medical University, Wenzhou 325035, Zhejiang Province, China
    2.Institute of Clinical Pharmacology, Peking University First Hospital, Beijing 100034, China
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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