Can Liu , Ru Qiao , Peng He , Wang Chen , Xiangting Gao , Fuyuan He
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Bioinformatic validation included immunohistochemistry, survival analysis, and immune infiltration profiling. Compound-protein interactions and structural stability were assessed via molecular docking and molecular dynamics simulations.</div></div><div><h3>Results</h3><div>We identified 2378 overlapping genes between AA and HCC. Enrichment analyses revealed significant activation of proteasome, cell cycle, and antigen processing pathways. PSMB4 was prioritized as a core gene, overexpressed in HCC tissues, associated with poor prognosis (HR = 1.69, <em>p</em> < 0.05), and strongly correlated with regulatory T cell and M2 macrophage infiltration. Docking and MD simulations confirmed strong and stable binding (−8.7 kcal/mol) between AA and PSMB4.</div></div><div><h3>Conclusion</h3><div>This study establishes a potential mechanistic connection between AA and HCC using an integrated network toxicology and machine learning, offering novel insights into toxicant-driven hepatocarcinogenesis and potential therapeutic targets.</div></div>","PeriodicalId":23289,"journal":{"name":"Toxicon","volume":"267 ","pages":"Article 108576"},"PeriodicalIF":2.4000,"publicationDate":"2025-09-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Mechanistic insights into aristolochic acid-induced hepatocellular carcinoma: a multi-dimensional analysis integrating network toxicology, machine learning, and molecular dynamics simulation\",\"authors\":\"Can Liu , Ru Qiao , Peng He , Wang Chen , Xiangting Gao , Fuyuan He\",\"doi\":\"10.1016/j.toxicon.2025.108576\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><div>Aristolochic acids (AA) are naturally occurring carcinogens found in traditional herbal medicines derived from <em>Aristolochia</em> species. This study explores the potential link between AA and hepatocellular carcinoma (HCC), aiming to uncover key molecular targets driving AA-induced hepatocarcinogenesis.</div></div><div><h3>Methods</h3><div>Toxicogenomic databases were used to identify AA-related toxicological profiles and targets, which were integrated with HCC-associated gene datasets. Protein-protein interaction networks were constructed, followed by enrichment analyses. A multi-machine learning framework was applied to prioritize candidate genes. Bioinformatic validation included immunohistochemistry, survival analysis, and immune infiltration profiling. Compound-protein interactions and structural stability were assessed via molecular docking and molecular dynamics simulations.</div></div><div><h3>Results</h3><div>We identified 2378 overlapping genes between AA and HCC. Enrichment analyses revealed significant activation of proteasome, cell cycle, and antigen processing pathways. PSMB4 was prioritized as a core gene, overexpressed in HCC tissues, associated with poor prognosis (HR = 1.69, <em>p</em> < 0.05), and strongly correlated with regulatory T cell and M2 macrophage infiltration. Docking and MD simulations confirmed strong and stable binding (−8.7 kcal/mol) between AA and PSMB4.</div></div><div><h3>Conclusion</h3><div>This study establishes a potential mechanistic connection between AA and HCC using an integrated network toxicology and machine learning, offering novel insights into toxicant-driven hepatocarcinogenesis and potential therapeutic targets.</div></div>\",\"PeriodicalId\":23289,\"journal\":{\"name\":\"Toxicon\",\"volume\":\"267 \",\"pages\":\"Article 108576\"},\"PeriodicalIF\":2.4000,\"publicationDate\":\"2025-09-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Toxicon\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0041010125003514\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Toxicon","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0041010125003514","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0
摘要
背景:马兜铃酸(AA)是一种在马兜铃属植物中发现的天然致癌物。本研究探讨了AA与肝细胞癌(HCC)之间的潜在联系,旨在揭示AA诱导肝癌发生的关键分子靶点。方法:利用毒理基因组数据库鉴定aa相关毒理学特征和靶点,并将其与hcc相关基因数据集相结合。构建蛋白-蛋白相互作用网络,然后进行富集分析。应用多机器学习框架对候选基因进行优先排序。生物信息学验证包括免疫组织化学、生存分析和免疫浸润谱。通过分子对接和分子动力学模拟评估化合物-蛋白质相互作用和结构稳定性。结果:我们发现了2378个AA和HCC之间的重叠基因。富集分析显示蛋白酶体、细胞周期和抗原加工途径的显著活化。PSMB4被优先作为核心基因,在HCC组织中过表达,与预后不良相关(HR = 1.69, p < 0.05),与调节性T细胞和M2巨噬细胞浸润密切相关。对接和MD模拟证实了AA和PSMB4之间强而稳定的结合(-8.7 kcal/mol)。结论:本研究通过综合网络毒理学和机器学习建立了AA和HCC之间的潜在机制联系,为毒物驱动的肝癌发生和潜在的治疗靶点提供了新的见解。
Mechanistic insights into aristolochic acid-induced hepatocellular carcinoma: a multi-dimensional analysis integrating network toxicology, machine learning, and molecular dynamics simulation
Background
Aristolochic acids (AA) are naturally occurring carcinogens found in traditional herbal medicines derived from Aristolochia species. This study explores the potential link between AA and hepatocellular carcinoma (HCC), aiming to uncover key molecular targets driving AA-induced hepatocarcinogenesis.
Methods
Toxicogenomic databases were used to identify AA-related toxicological profiles and targets, which were integrated with HCC-associated gene datasets. Protein-protein interaction networks were constructed, followed by enrichment analyses. A multi-machine learning framework was applied to prioritize candidate genes. Bioinformatic validation included immunohistochemistry, survival analysis, and immune infiltration profiling. Compound-protein interactions and structural stability were assessed via molecular docking and molecular dynamics simulations.
Results
We identified 2378 overlapping genes between AA and HCC. Enrichment analyses revealed significant activation of proteasome, cell cycle, and antigen processing pathways. PSMB4 was prioritized as a core gene, overexpressed in HCC tissues, associated with poor prognosis (HR = 1.69, p < 0.05), and strongly correlated with regulatory T cell and M2 macrophage infiltration. Docking and MD simulations confirmed strong and stable binding (−8.7 kcal/mol) between AA and PSMB4.
Conclusion
This study establishes a potential mechanistic connection between AA and HCC using an integrated network toxicology and machine learning, offering novel insights into toxicant-driven hepatocarcinogenesis and potential therapeutic targets.
期刊介绍:
Toxicon has an open access mirror Toxicon: X, sharing the same aims and scope, editorial team, submission system and rigorous peer review. An introductory offer Toxicon: X - full waiver of the Open Access fee.
Toxicon''s "aims and scope" are to publish:
-articles containing the results of original research on problems related to toxins derived from animals, plants and microorganisms
-papers on novel findings related to the chemical, pharmacological, toxicological, and immunological properties of natural toxins
-molecular biological studies of toxins and other genes from poisonous and venomous organisms that advance understanding of the role or function of toxins
-clinical observations on poisoning and envenoming where a new therapeutic principle has been proposed or a decidedly superior clinical result has been obtained.
-material on the use of toxins as tools in studying biological processes and material on subjects related to venom and antivenom problems.
-articles on the translational application of toxins, for example as drugs and insecticides
-epidemiological studies on envenoming or poisoning, so long as they highlight a previously unrecognised medical problem or provide insight into the prevention or medical treatment of envenoming or poisoning. Retrospective surveys of hospital records, especially those lacking species identification, will not be considered for publication. Properly designed prospective community-based surveys are strongly encouraged.
-articles describing well-known activities of venoms, such as antibacterial, anticancer, and analgesic activities of arachnid venoms, without any attempt to define the mechanism of action or purify the active component, will not be considered for publication in Toxicon.
-review articles on problems related to toxinology.
To encourage the exchange of ideas, sections of the journal may be devoted to Short Communications, Letters to the Editor and activities of the affiliated societies.