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Exploration the mechanism of ATF3 participating in cell senescence of hypertensive nephropathy based on bioinformatics analysis
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Yu CHEN1, 2, Zhi-wei QIU2, Xin LUO1, 2, Jia-jia WANG2, 3, Qian XIANG1, 2
Chinese Journal of Clinical Pharmacology | 2025, 41(8) : 1175 - 1179
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Chinese Journal of Clinical Pharmacology | 2025, 41(8): 1175-1179
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Exploration the mechanism of ATF3 participating in cell senescence of hypertensive nephropathy based on bioinformatics analysis
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Yu CHEN1, 2, Zhi-wei QIU2, Xin LUO1, 2, Jia-jia WANG2, 3, Qian XIANG1, 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
  • 3.School of Pharmacy, Xuzhou Medical University, Xuzhou 221004, Jiangsu Province, China
Published: 2025-04-28 doi: 10.13699/j.cnki.1001-6821.2025.08.022
Outline
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Objective

To study the possible mechanism and related signaling pathway of cell senescence in hypertensive nephropathy with the help of bioinformatics.

Methods

The microarray data GSE37455 was downloaded from the gene expression database, and the data was merged with R software to remove the batch effect, so as to obtain differentially expressed genes. Cell aging genes were obtained from the CellAge database, and differential genes related to cell aging were obtained through R package “ggVennDiagram”. Gene interaction network string database was imported to obtain protein protein interaction (PPI) network map, and Cytoscape3.8.0 software was used to mine core differential genes. The function and pathway of core differential genes were analyzed by gene ontology (GO), Kyoto encyclopedia of genes and genomes (KEGG) and gene set enrichment analysis (GSEA).

Results

A total of 41 differential genes were obtained, including 32 up-regulated genes and 9 down-regulated genes. Four differential genes related to cell senescence were obtained after intersection. The core differential gene-activated transcription factor 3(ATF3) was obtained by PPI analysis and Cytoscape treatment. GSEA analysis showed that cell senescence might play a role in hypertensive nephropathy through the thermogenesis of mitochondrial uncoupling protein 1 and the signal transduction of type Ⅰ interferon response (TYPE-Ⅰ-IFN).

Conclusion

Cellular senescence may play a role in hypertensive nephropathy through pathways such as mitochondrial uncoupling protein-1 thermogenesis and TYPE-Ⅰ-IFN signaling, which provides a therapeutic target for the study of hypertensive nephropathy.

hypertensive nephropathy  /  cellular senescence  /  differentially expressed genes  /  bioinformatics  /  mechanism of action
Yu CHEN, Zhi-wei QIU, Xin LUO, Jia-jia WANG, Qian XIANG. Exploration the mechanism of ATF3 participating in cell senescence of hypertensive nephropathy based on bioinformatics analysis[J]. Chinese Journal of Clinical Pharmacology, 2025 , 41 (8) : 1175 -1179 . DOI: 10.13699/j.cnki.1001-6821.2025.08.022
Year 2025 volume 41 Issue 8
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Article Info
doi: 10.13699/j.cnki.1001-6821.2025.08.022
  • Receive Date:2024-11-09
  • Online Date:2026-08-05
  • Published:2025-04-28
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  • Received:2024-11-09
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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
    3.School of Pharmacy, Xuzhou Medical University, Xuzhou 221004, Jiangsu Province, 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
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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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