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The potential mechanism of platelet factor 4 in Alzheimer’s disease explored by bioinformatics analysis
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Jing NIU1, 2, Long-tu LI1, Jia-jia WANG1, 2, Qian Xiang1, 2, Zhi-yan LIU1
Chinese Journal of Clinical Pharmacology | 2025, 41(17) : 2521 - 2525
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Chinese Journal of Clinical Pharmacology | 2025, 41(17): 2521-2525
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The potential mechanism of platelet factor 4 in Alzheimer’s disease explored by bioinformatics analysis
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Jing NIU1, 2, Long-tu LI1, Jia-jia WANG1, 2, Qian Xiang1, 2, Zhi-yan LIU1
Affiliations
  • 1.Institute of Clinical Pharmacology, Peking University First Hospital, Beijing 100034, China
  • 2.School of Pharmacy, Xuzhou Medical University, Xuzhou 221004, Jiangsu Province, China
Published: 2025-09-17 doi: 10.13699/j.cnki.1001-6821.2025.17.021
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Objective

To explore the potential role of platelet factor 4 (PF4) in Alzheimer’s disease (AD) by network pharmacology and bioinformatics analysis.

Methods

PubChem and SwissTargetPrediction databases were used to collect PF4 related targets, GeneCards and DisGeNET databases were used to collect AD targets; the protein-protein interaction (PPI) network was constructed by using STRING database to obtain the protein-protein interaction of common genes. Gene ontology (GO) function and Kyoto encyclopedia of genes and genomes (KEGG) pathway enrichment analysis of common targets were performed using DAVID database. The VascularSingleCells database was used to query the expression of PF4 in mouse cerebrovascular-related cells, and the AlzData database was used to analyze the verification of PF4 in the data set of known AD patients.

Results

A total of 102 PF4-related targets, 2 403 AD targets and 51 common targets were obtained. Enrichment analysis showed that the common argets were mainly involved in cancer pathways, neutrophil extracellular trap formation, Interleukin-17 (IL-17) signaling pathway, platelet activation and relaxin signaling pathway. Analysis of cerebrovascular single cell data showed that PF4 was only expressed in microglia. The results of HPA database analysis showed that PF4 was mainly expressed in the cerebral cortex, and a small part was expressed in the amygdala.

Conclusion

PF4 may interfere with AD by improving neuronal viability, oxidative stress and reducing inflammatory response through neutrophil extracellular trapping network formation, IL-17 signaling and other pathways.

platelet factor 4  /  Alzheimer’s disease  /  network pharmacology  /  biographical analysis
Jing NIU, Long-tu LI, Jia-jia WANG, Qian Xiang, Zhi-yan LIU. The potential mechanism of platelet factor 4 in Alzheimer’s disease explored by bioinformatics analysis[J]. Chinese Journal of Clinical Pharmacology, 2025 , 41 (17) : 2521 -2525 . DOI: 10.13699/j.cnki.1001-6821.2025.17.021
Year 2025 volume 41 Issue 17
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doi: 10.13699/j.cnki.1001-6821.2025.17.021
  • Receive Date:2024-06-03
  • Online Date:2026-08-05
  • Published:2025-09-17
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  • Received:2024-06-03
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Affiliations
    1.Institute of Clinical Pharmacology, Peking University First Hospital, Beijing 100034, China
    2.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
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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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