喜黄丸通过调节肠道菌群、调节甘油磷脂代谢、促进自噬稳态发挥抗三阴性乳腺癌作用。

IF 3.1 3区 医学 Q2 CHEMISTRY, ANALYTICAL
Yuanyuan Gu , Yue Wang , Guangyou Qu , Youfei Pen , Yiming Chen , Xiubo Zhu , Yuanyuan Li , Yang Wang , Fang Fang , Shuxiang Zhang , Fang Lu
{"title":"喜黄丸通过调节肠道菌群、调节甘油磷脂代谢、促进自噬稳态发挥抗三阴性乳腺癌作用。","authors":"Yuanyuan Gu ,&nbsp;Yue Wang ,&nbsp;Guangyou Qu ,&nbsp;Youfei Pen ,&nbsp;Yiming Chen ,&nbsp;Xiubo Zhu ,&nbsp;Yuanyuan Li ,&nbsp;Yang Wang ,&nbsp;Fang Fang ,&nbsp;Shuxiang Zhang ,&nbsp;Fang Lu","doi":"10.1016/j.jpba.2025.117166","DOIUrl":null,"url":null,"abstract":"<div><div>Triple-negative breast cancer (TNBC) is the most aggressive molecular subtype of breast cancer, characterized by high malignancy and poor prognosis. Xihuang Pill (XHP), a traditional Chinese medicine (TCM) formulation, has demonstrated therapeutic efficacy against TNBC. This study investigates the antitumor mechanisms and therapeutic potential of XHP. The chemical composition of XHP was analyzed using ultra-performance liquid chromatography-mass spectrometry (UPLC-MS). The murine TNBC model was established via orthotopic implantation of 4T1 cells, followed by XHP treatment. Multi-omics analyses including gut microbiota profiling, metabolomics, and molecular biology approaches were conducted, along with the use of a pseudo-germ-free mouse model.XHP inhibited TNBC cell proliferation, induced apoptosis, and suppressed tumor growth, while also enhancing immune function, as evidenced by an increased CD4 + /CD8 + T-cell ratio. Integrated analysis identified four key bacterial genera (Deferribacterota, Mucispirillum, Eisenbergiella, and Monoglobus) and 13 metabolites involved in glycerophospholipid metabolism. XHP downregulated PCYT1A and PCYT2, key enzymes in this pathway. However, antibiotic-induced depletion of gut microbiota abolished XHP’s antitumor and metabolic regulatory effects. Furthermore, XHP enhanced autophagy, as indicated by an increased LC3-II/I ratio and decreased p62 expression.In conclusion, XHP exerts antitumor effects against TNBC by modulating gut microbiota-dependent glycerophospholipid metabolism and restoring autophagy homeostasis. These findings provide novel insights into the anticancer mechanisms of TCM by elucidating microecological–metabolic interactions.</div></div>","PeriodicalId":16685,"journal":{"name":"Journal of pharmaceutical and biomedical analysis","volume":"267 ","pages":"Article 117166"},"PeriodicalIF":3.1000,"publicationDate":"2025-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Xi Huang Pill exerts anti-triple-negative breast cancer effects by modulating gut microbiota, regulating glycerophospholipid metabolism, and promoting autophagy homeostasis\",\"authors\":\"Yuanyuan Gu ,&nbsp;Yue Wang ,&nbsp;Guangyou Qu ,&nbsp;Youfei Pen ,&nbsp;Yiming Chen ,&nbsp;Xiubo Zhu ,&nbsp;Yuanyuan Li ,&nbsp;Yang Wang ,&nbsp;Fang Fang ,&nbsp;Shuxiang Zhang ,&nbsp;Fang Lu\",\"doi\":\"10.1016/j.jpba.2025.117166\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Triple-negative breast cancer (TNBC) is the most aggressive molecular subtype of breast cancer, characterized by high malignancy and poor prognosis. Xihuang Pill (XHP), a traditional Chinese medicine (TCM) formulation, has demonstrated therapeutic efficacy against TNBC. This study investigates the antitumor mechanisms and therapeutic potential of XHP. The chemical composition of XHP was analyzed using ultra-performance liquid chromatography-mass spectrometry (UPLC-MS). The murine TNBC model was established via orthotopic implantation of 4T1 cells, followed by XHP treatment. Multi-omics analyses including gut microbiota profiling, metabolomics, and molecular biology approaches were conducted, along with the use of a pseudo-germ-free mouse model.XHP inhibited TNBC cell proliferation, induced apoptosis, and suppressed tumor growth, while also enhancing immune function, as evidenced by an increased CD4 + /CD8 + T-cell ratio. Integrated analysis identified four key bacterial genera (Deferribacterota, Mucispirillum, Eisenbergiella, and Monoglobus) and 13 metabolites involved in glycerophospholipid metabolism. XHP downregulated PCYT1A and PCYT2, key enzymes in this pathway. However, antibiotic-induced depletion of gut microbiota abolished XHP’s antitumor and metabolic regulatory effects. Furthermore, XHP enhanced autophagy, as indicated by an increased LC3-II/I ratio and decreased p62 expression.In conclusion, XHP exerts antitumor effects against TNBC by modulating gut microbiota-dependent glycerophospholipid metabolism and restoring autophagy homeostasis. These findings provide novel insights into the anticancer mechanisms of TCM by elucidating microecological–metabolic interactions.</div></div>\",\"PeriodicalId\":16685,\"journal\":{\"name\":\"Journal of pharmaceutical and biomedical analysis\",\"volume\":\"267 \",\"pages\":\"Article 117166\"},\"PeriodicalIF\":3.1000,\"publicationDate\":\"2025-09-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of pharmaceutical and biomedical analysis\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0731708525005072\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, ANALYTICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of pharmaceutical and biomedical analysis","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0731708525005072","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0

摘要

三阴性乳腺癌(TNBC)是乳腺癌中最具侵袭性的分子亚型,其特点是恶性程度高,预后差。西黄丸(XHP)是一种中药制剂,具有治疗TNBC的疗效。本研究探讨XHP的抗肿瘤机制和治疗潜力。采用超高效液相色谱-质谱(UPLC-MS)分析XHP的化学成分。通过原位植入4T1细胞建立小鼠TNBC模型,然后用XHP处理。多组学分析包括肠道微生物群分析,代谢组学和分子生物学方法,以及使用伪无菌小鼠模型。XHP抑制TNBC细胞增殖,诱导细胞凋亡,抑制肿瘤生长,同时增强免疫功能,CD4 + /CD8 + t细胞比例增加。综合分析确定了4个关键细菌属(铁杆菌属、Mucispirillum、Eisenbergiella和Monoglobus)和13个参与甘油磷脂代谢的代谢物。XHP下调PCYT1A和PCYT2,这是该途径的关键酶。然而,抗生素引起的肠道菌群耗竭消除了XHP的抗肿瘤和代谢调节作用。此外,XHP增强了自噬,LC3-II/I比值升高,p62表达降低。综上所述,XHP通过调节肠道微生物依赖的甘油磷脂代谢和恢复自噬稳态来发挥对TNBC的抗肿瘤作用。这些发现通过阐明微生态-代谢相互作用,为中医药抗癌机制提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Xi Huang Pill exerts anti-triple-negative breast cancer effects by modulating gut microbiota, regulating glycerophospholipid metabolism, and promoting autophagy homeostasis
Triple-negative breast cancer (TNBC) is the most aggressive molecular subtype of breast cancer, characterized by high malignancy and poor prognosis. Xihuang Pill (XHP), a traditional Chinese medicine (TCM) formulation, has demonstrated therapeutic efficacy against TNBC. This study investigates the antitumor mechanisms and therapeutic potential of XHP. The chemical composition of XHP was analyzed using ultra-performance liquid chromatography-mass spectrometry (UPLC-MS). The murine TNBC model was established via orthotopic implantation of 4T1 cells, followed by XHP treatment. Multi-omics analyses including gut microbiota profiling, metabolomics, and molecular biology approaches were conducted, along with the use of a pseudo-germ-free mouse model.XHP inhibited TNBC cell proliferation, induced apoptosis, and suppressed tumor growth, while also enhancing immune function, as evidenced by an increased CD4 + /CD8 + T-cell ratio. Integrated analysis identified four key bacterial genera (Deferribacterota, Mucispirillum, Eisenbergiella, and Monoglobus) and 13 metabolites involved in glycerophospholipid metabolism. XHP downregulated PCYT1A and PCYT2, key enzymes in this pathway. However, antibiotic-induced depletion of gut microbiota abolished XHP’s antitumor and metabolic regulatory effects. Furthermore, XHP enhanced autophagy, as indicated by an increased LC3-II/I ratio and decreased p62 expression.In conclusion, XHP exerts antitumor effects against TNBC by modulating gut microbiota-dependent glycerophospholipid metabolism and restoring autophagy homeostasis. These findings provide novel insights into the anticancer mechanisms of TCM by elucidating microecological–metabolic interactions.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
6.70
自引率
5.90%
发文量
588
审稿时长
37 days
期刊介绍: This journal is an international medium directed towards the needs of academic, clinical, government and industrial analysis by publishing original research reports and critical reviews on pharmaceutical and biomedical analysis. It covers the interdisciplinary aspects of analysis in the pharmaceutical, biomedical and clinical sciences, including developments in analytical methodology, instrumentation, computation and interpretation. Submissions on novel applications focusing on drug purity and stability studies, pharmacokinetics, therapeutic monitoring, metabolic profiling; drug-related aspects of analytical biochemistry and forensic toxicology; quality assurance in the pharmaceutical industry are also welcome. Studies from areas of well established and poorly selective methods, such as UV-VIS spectrophotometry (including derivative and multi-wavelength measurements), basic electroanalytical (potentiometric, polarographic and voltammetric) methods, fluorimetry, flow-injection analysis, etc. are accepted for publication in exceptional cases only, if a unique and substantial advantage over presently known systems is demonstrated. The same applies to the assay of simple drug formulations by any kind of methods and the determination of drugs in biological samples based merely on spiked samples. Drug purity/stability studies should contain information on the structure elucidation of the impurities/degradants.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信