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首页|期刊导航|癌变·畸变·突变|基于网络毒理学和分子对接探讨双酚S、双酚E和双酚AF诱导神经毒性的协同作用机制

基于网络毒理学和分子对接探讨双酚S、双酚E和双酚AF诱导神经毒性的协同作用机制

曾品利 王忠 罗贵明 王志秋 李灏 黄琰 卜迁

癌变·畸变·突变2026,Vol.38Issue(3):205-211,7.
癌变·畸变·突变2026,Vol.38Issue(3):205-211,7.DOI:10.3969/j.issn.1004-616x.2026.03.005

基于网络毒理学和分子对接探讨双酚S、双酚E和双酚AF诱导神经毒性的协同作用机制

Synergistic neurotoxicity of bisphenol S,bisphenol E and bisphenol AF revealed by network toxicology and molecular docking

曾品利 1王忠 1罗贵明 1王志秋 1李灏 1黄琰 1卜迁1

作者信息

  • 1. 四川大学华西公共卫生学院/华西第四医院卫生毒理与病理学系,四川 成都 610041
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摘要

Abstract

OBJECTIVE:To investigate synergistic mechanisms through which bisphenol analogues—bisphenol S(BPS),bisphenol E(BPE),and bisphenol AF(BPAF)—induced neurotoxicity,and to provide a scientific foundation for evaluating their health risks.METHODS:Target genes for BPS,BPE,and BPAF were retrieved from four databases,including ChEMBL.Venn diagram analysis was performed to identify common targets,followed by intersection with neurotoxicity-related targets from the GeneCards database.Functional enrichment analysis of these intersected targets was conducted using the DAVID database,with results visualized in R.A protein-protein interaction(PPI)network was constructed using STRING,and network analysis was performed via Cytoscape.The CytoHubba plugin was used to calculate maximum cluster centrality(MCC)values,and the top 10 targets ranked by both degree centrality and MCC were selected as core targets.The 3D structures of BPS,BPE,and BPAF were obtained from the PubChem database,while the crystal structures of core target proteins were retrieved from PDB.Molecular docking was performed using the CB-Dock2 and visualized in PyMOL.RESULTS:The common targets of neurotoxicity induced by BPS,BPE,and BPAF were significantly enriched in pathways such as MAPK.Core targets included ALB,TNF,CASP3,ESR1,IGF1,EGFR,MMP9,and SRC.All three bisphenols exhibited strong binding affinities(Vina scores<-6 kcal/mol),with BPAF showing greater affinity than BPS and BPE.CONCLUSION:BPS,BPE,and BPAF induced neuroinflammation and apoptosis through synergistic regulation of multiple pathways,including MAPK,thereby leading to neurotoxicity.Among them,BPAF demonstrated stronger effects,highlighting its increased neurotoxic risk.

关键词

双酚S/双酚E/双酚AF/神经毒性/网络毒理学

Key words

bisphenol S/bisphenol E/bisphenol AF/neurotoxicity/network toxicology

分类

医药卫生

引用本文复制引用

曾品利,王忠,罗贵明,王志秋,李灏,黄琰,卜迁..基于网络毒理学和分子对接探讨双酚S、双酚E和双酚AF诱导神经毒性的协同作用机制[J].癌变·畸变·突变,2026,38(3):205-211,7.

基金项目

四川省自然科学基金面上项目(2024NSFSC0707) (2024NSFSC0707)

癌变·畸变·突变

1004-616X

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