Evidence map›Paper›PMID 41742320›Full record

ArticleBMC pharmacology & toxicology2026

Investigating the mechanisms by which bisphenol A affects osteoarthritis through a novel network toxicology framework and experimental validation.

Qiwang He, Shanlang Li, Yining Chen, Yue Liu, Yang Li, Shuqi Min, Shenlong Yi, Feng Li, Xiaohong Zhou

Abstract read
In one paragraph

Article in BMC pharmacology & toxicology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Qiwang He *Hubei University of Chinese Medicine, Wuhan, 430061, China.
Shanlang Li *Key Laboratory of Clinical Cohort Research on Bone and Joint Degenerative Diseases of Guangxi, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, 533000, China.
Yining Chen *Fujian University of Traditional Chinese Medicine, Fuzhou, 350108, China.
Yue LiuGeneral Hospital of Western Theater Command, Chengdu, 610083, China.
Yang LiHubei University of Chinese Medicine, Wuhan, 430061, China.
Shuqi MinChangzhou Hospital of Traditional Chinese Medicine, Affiliated Hospital of Nanjing University of Chinese Medicine, Changzhou, 213000, China.
Shenlong YiHubei University of Chinese Medicine, Wuhan, 430061, China.
Feng LiHubei University of Chinese Medicine, Wuhan, 430061, China.
Xiaohong ZhouHubei University of Chinese Medicine, Wuhan, 430061, China. 1686090116@qq.com.

Funding

National Natural Science Foundation of China (82405573Postgraduate Research & Practice Innovation Program of Jiangsu Province SJCX24_1026Young and Middle-aged Backbone Talents Project of Youjiang Medical University for Nationalities Affiliated Hospital Y202210310
6 · The paper itself

Abstract

backgroundIn this study, we adopted network toxicology approaches to explore the potential risk effects of bisphenol A (BPA) on osteoarthritis (OA) processes.

methodsTargets related to BPA were obtained from the ChEMBL, Swiss Target Prediction, and STITCH databases, and OA-related targets were obtained from the GeneCards, DisGeNET, and OMIM databases; using the obtained information, we identified common targets. Then, the core targets were determined using the STRING database and the Cytoscape software, and functional enrichment analysis was subsequently conducted to elucidate the potential mechanisms. Moreover, a comprehensive validation of the core targets was conducted through molecular docking and dynamics simulations. Moreover, clinical samples were collected for experimental validation.

resultsA total of 88 overlapping targets were identified, and six core targets (SRC, ESR1, EGFR, PTGS2, PPARG, and HSP90AA1) were further screened. The results of the enrichment analysis revealed that the main pathways through which BPA affects OA involve key signaling cascades, including the estrogen signaling pathway, the thyroid hormone signaling pathway, and the ErbB signaling pathway. The results of molecular docking and dynamic simulations indicated that there are stable binding interactions between BPA and the core targets. The results of the RT-qPCR and IHC assays revealed significant differences in the core targets between the OA group and the normal group.

conclusionsThis study links the environmental toxin BPA with OA, systematically describing potential core targets and pathways. These findings emphasize the importance of reducing BPA exposure in public health, providing new insights for the formulation of subsequent environmental policies.

trial registrationNot applicable.

Indexed as

Benzhydryl CompoundsEndocrine DisruptorsOsteoarthritisPhenolsBisphenol A CompoundsHumansMolecular Docking SimulationMolecular Dynamics SimulationSignal TransductionBenzhydryl Compoundsbisphenol ABisphenol A CompoundsEndocrine DisruptorsPhenolsBisphenol AExperimental validationMolecular dynamics simulationNetwork toxicologyOsteoarthritis

Identifiers

PMID41742320
PMCPMC13040831

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.