• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

基于网络药理学、分子对接和体外实验对纳西族传统草药配方抗肝癌作用的研究

An Investigation of the Effect of the Traditional Naxi Herbal Formula Against Liver Cancer Through Network Pharmacology, Molecular Docking, and In Vitro Experiments.

作者信息

Yan Xiuxiang, Inta Angkhana, Yang Xuefei, Pandith Hataichanok, Disayathanoowat Terd, Yang Lixin

机构信息

Key Laboratory of Economic Plants and Biotechnology, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China.

Department of Biology, Faculty of Science, Chiang Mai University, 239 Huay Kaew Road, Chiang Mai 50200, Thailand.

出版信息

Pharmaceuticals (Basel). 2024 Oct 25;17(11):1429. doi: 10.3390/ph17111429.

DOI:10.3390/ph17111429
PMID:39598341
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11597843/
Abstract

: The formula Chong-Lou-Yao-Fang (CLYF) is an herbal medicinal formulation developed by the indigenous Naxi people for treating liver cancer. This study was to reveal the biological activity, potential targets, and molecular mechanisms of CLYF for cancer treatment. : Network pharmacology, microarray data analysis, survival analysis, and molecular docking were employed to predict potential compounds, targets, and pathways for the treatment of liver cancer. In vitro experiments and Western blot validation were conducted to confirm these predictions. : 35 key compounds and 20 core targets were screened from CLYF, involving signaling pathways for PI3K-Akt, MAPK, hepatitis B and C, which were effective for liver cancer treatment. Microarray data analysis and survival analysis indicated that EGFR and TP53 serve as promising biomarkers for diagnosis and prognosis in liver cancer. Molecular docking revealed stable binding between EGFR, TP53, and AKT1 with active ingredients. Cell experiments confirmed that CLYF-A suppressed cell proliferation, induced apoptosis, and caused cell cycle arrest in HepG2 cells, which were associated with a loss of mitochondrial membrane potential. Compared to the control group, the relative protein expression levels of EGFR and AKT1 significantly decreased following treatment with CLYF-A, while TP53 levels increased significantly. : Verification of the anticancer activity of CLYF and its potential mechanisms may have important implications for anticancer therapies. Our results may provide a scientific basis for the clinical use of CLYF for cancer treatment and have important implications for developing pharmaceutical preparations, which also need more pharmacological experiments, clinical experiments, and in vivo experiments.

摘要

重楼瑶方(CLYF)是纳西族本土研发的一种用于治疗肝癌的草药配方。本研究旨在揭示CLYF治疗癌症的生物学活性、潜在靶点和分子机制。采用网络药理学、微阵列数据分析、生存分析和分子对接来预测治疗肝癌的潜在化合物、靶点和通路。进行体外实验和蛋白质印迹验证以证实这些预测。从CLYF中筛选出35种关键化合物和20个核心靶点,涉及PI3K-Akt、MAPK、乙型和丙型肝炎信号通路,这些对肝癌治疗有效。微阵列数据分析和生存分析表明,EGFR和TP53有望作为肝癌诊断和预后的生物标志物。分子对接揭示了EGFR、TP53和AKT1与活性成分之间的稳定结合。细胞实验证实,CLYF-A抑制HepG2细胞增殖、诱导凋亡并导致细胞周期停滞,这与线粒体膜电位丧失有关。与对照组相比,CLYF-A处理后EGFR和AKT1的相对蛋白表达水平显著降低,而TP53水平显著升高。CLYF抗癌活性及其潜在机制的验证可能对抗癌治疗具有重要意义。我们的结果可能为CLYF在癌症治疗中的临床应用提供科学依据,并对开发药物制剂具有重要意义,这也需要更多的药理实验、临床实验和体内实验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00ae/11597843/bf0517b137a4/pharmaceuticals-17-01429-g014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00ae/11597843/c9a92f24103b/pharmaceuticals-17-01429-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00ae/11597843/8aeb0db787dc/pharmaceuticals-17-01429-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00ae/11597843/b7423666fccc/pharmaceuticals-17-01429-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00ae/11597843/fb976f8bed81/pharmaceuticals-17-01429-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00ae/11597843/593045a9e812/pharmaceuticals-17-01429-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00ae/11597843/96844f7e5608/pharmaceuticals-17-01429-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00ae/11597843/3771b612c06a/pharmaceuticals-17-01429-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00ae/11597843/06d10da73129/pharmaceuticals-17-01429-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00ae/11597843/f67d29beb3d5/pharmaceuticals-17-01429-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00ae/11597843/2d9c4b09a866/pharmaceuticals-17-01429-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00ae/11597843/da46ad7ddec6/pharmaceuticals-17-01429-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00ae/11597843/7a12e69f64c1/pharmaceuticals-17-01429-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00ae/11597843/0e650f4099f9/pharmaceuticals-17-01429-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00ae/11597843/bf0517b137a4/pharmaceuticals-17-01429-g014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00ae/11597843/c9a92f24103b/pharmaceuticals-17-01429-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00ae/11597843/8aeb0db787dc/pharmaceuticals-17-01429-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00ae/11597843/b7423666fccc/pharmaceuticals-17-01429-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00ae/11597843/fb976f8bed81/pharmaceuticals-17-01429-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00ae/11597843/593045a9e812/pharmaceuticals-17-01429-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00ae/11597843/96844f7e5608/pharmaceuticals-17-01429-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00ae/11597843/3771b612c06a/pharmaceuticals-17-01429-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00ae/11597843/06d10da73129/pharmaceuticals-17-01429-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00ae/11597843/f67d29beb3d5/pharmaceuticals-17-01429-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00ae/11597843/2d9c4b09a866/pharmaceuticals-17-01429-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00ae/11597843/da46ad7ddec6/pharmaceuticals-17-01429-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00ae/11597843/7a12e69f64c1/pharmaceuticals-17-01429-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00ae/11597843/0e650f4099f9/pharmaceuticals-17-01429-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00ae/11597843/bf0517b137a4/pharmaceuticals-17-01429-g014.jpg

相似文献

1
An Investigation of the Effect of the Traditional Naxi Herbal Formula Against Liver Cancer Through Network Pharmacology, Molecular Docking, and In Vitro Experiments.基于网络药理学、分子对接和体外实验对纳西族传统草药配方抗肝癌作用的研究
Pharmaceuticals (Basel). 2024 Oct 25;17(11):1429. doi: 10.3390/ph17111429.
2
A network pharmacology approach and experimental validation to investigate the anticancer mechanism and potential active targets of ethanol extract of Wei-Tong-Xin against colorectal cancer through induction of apoptosis via PI3K/AKT signaling pathway.基于网络药理学方法和实验验证,探讨味通心通过诱导 PI3K/AKT 信号通路细胞凋亡对结肠癌的抗癌机制和潜在的活性靶点。
J Ethnopharmacol. 2023 Mar 1;303:115933. doi: 10.1016/j.jep.2022.115933. Epub 2022 Nov 18.
3
Understanding apoptotic induction by Sargentodoxa cuneata-Patrinia villosa herb pair via PI3K/AKT/mTOR signalling in colorectal cancer cells using network pharmacology and cellular studies.采用网络药理学和细胞研究方法探讨山乌龟-败酱草药对对结直肠癌细胞中 PI3K/AKT/mTOR 信号通路诱导细胞凋亡的作用机制。
J Ethnopharmacol. 2024 Jan 30;319(Pt 3):117342. doi: 10.1016/j.jep.2023.117342. Epub 2023 Oct 23.
4
Network pharmacology, molecular docking and experimental study of CEP in nasopharyngeal carcinoma.基于网络药理学、分子对接及实验研究探讨鼻咽癌细胞中 CEP 的作用机制
J Ethnopharmacol. 2024 Apr 6;323:117667. doi: 10.1016/j.jep.2023.117667. Epub 2023 Dec 28.
5
Jian Pi Hua Tan Fang Reverses Trastuzumab Resistance of HER2-Positive Gastric Cancer Through PI3K/AKT/mTOR Pathway: Integrating Network Pharmacology, Molecular Docking and Experimental Validation.健脾化痰方通过PI3K/AKT/mTOR通路逆转HER2阳性胃癌的曲妥珠单抗耐药性:整合网络药理学、分子对接和实验验证
Immun Inflamm Dis. 2025 Feb;13(2):e70154. doi: 10.1002/iid3.70154.
6
[Mechanism of n-butanol fraction of Wenxia Formula combining with gefitinib in treating non-small cell lung cancer based on network pharmacology and in vitro experiment].基于网络药理学和体外实验探讨温夏方正丁醇部位联合吉非替尼治疗非小细胞肺癌的作用机制
Zhongguo Zhong Yao Za Zhi. 2024 Jan;49(2):471-486. doi: 10.19540/j.cnki.cjcmm.20230914.704.
7
Network Pharmacology Based Elucidation of Molecular Mechanisms of Laoke Formula for Treatment of Advanced Non-Small Cell Lung Cancer.基于网络药理学的老柯方治疗晚期非小细胞肺癌作用机制的研究。
Chin J Integr Med. 2024 Nov;30(11):984-992. doi: 10.1007/s11655-024-3717-5. Epub 2024 Jun 28.
8
Network pharmacology analysis, molecular docking integrated experimental verification reveal β-sitosterol as the active anti-NSCLC ingredient of Polygonatum cyrtonema Hua by suppression of PI3K/Akt/HIF-1α signaling pathway.网络药理学分析、分子对接实验验证表明,β-谷甾醇通过抑制 PI3K/Akt/HIF-1α 信号通路成为玉竹中抗非小细胞肺癌的活性成分。
J Ethnopharmacol. 2024 Jun 28;328:117900. doi: 10.1016/j.jep.2024.117900. Epub 2024 Mar 1.
9
Study on the Potential Mechanism of Tonifying Kidney and Removing Dampness Formula in the Treatment of Postmenopausal Dyslipidemia Based on Network Pharmacology, Molecular Docking and Experimental Evidence.基于网络药理学、分子对接和实验证据的补肾祛湿方治疗绝经后血脂异常的潜在机制研究。
Front Endocrinol (Lausanne). 2022 Jul 7;13:918469. doi: 10.3389/fendo.2022.918469. eCollection 2022.
10
Network pharmacology, molecular docking and experimental verification of the mechanism of huangqi-jixuecao herb pair in treatment of peritoneal fibrosis.黄芪鸡血藤药对治疗腹膜纤维化机制的网络药理学、分子对接及实验验证。
J Ethnopharmacol. 2024 Jan 10;318(Pt A):116874. doi: 10.1016/j.jep.2023.116874. Epub 2023 Jul 10.

引用本文的文献

1
Mitophagy as a pivotal axis in non‑alcoholic fatty liver disease: From pathogenic mechanisms to therapeutic strategies (Review).线粒体自噬作为非酒精性脂肪性肝病的关键轴:从发病机制到治疗策略(综述)
Mol Med Rep. 2025 Nov;32(5). doi: 10.3892/mmr.2025.13664. Epub 2025 Aug 29.
2
Molecular Mechanisms of var. Against Gastric Cancer: Metabolite Analysis, Signaling Pathways, and Protein Targets.var. 抗胃癌的分子机制:代谢物分析、信号通路及蛋白质靶点
Pharmaceuticals (Basel). 2025 May 30;18(6):823. doi: 10.3390/ph18060823.
3
Fermented Against Atopic Dermatitis Through AKT/mTOR and Jun Pathways.
通过AKT/mTOR和Jun信号通路对特应性皮炎产生抑制作用。 (推测原文Fermented有误,可能是Inhibited,按照纠正后的词意翻译)
Pharmaceuticals (Basel). 2024 Dec 27;18(1):20. doi: 10.3390/ph18010020.