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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.

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/c9a92f24103b/pharmaceuticals-17-01429-g001.jpg

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