Network Pharmacology and Molecular Docking Study on the Mechanism of the Therapeutic Effect of Strychni Semen in NSCLC.

IF 3.7 3区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
He Geng, Yujie Xue, Binghua Yan, Zhaoxue Lu, Hengjin Yang, Peng Li, Jundong Zhou
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引用次数: 0

Abstract

Strychni Semen, characterized by its bitter taste and warm properties, has been confirmed to possess anti-tumor properties. However, the molecular mechanism of Strychni Semen in treating non-small cell lung cancer (NSCLC) needs further study. This study aimed to explore the molecular mechanism of Strychni Semen in treating NSCLC based on network pharmacology and molecular docking. The active components and targets of Strychni Semen were retrieved from the TCMSP, supplemented by the HERB database and the related literature. NSCLC-related targets were retrieved from the GeneCards, OMIM and DisGenet databases. The intersection targets of Strychni Semen in treating NSCLC were obtained via an online platform. The Protein-Protein Interaction (PPI) network was subsequently constructed to deeply analyse the interrelationship of the intersection targets via the String database. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses were carried out via the Metascape database. The interactive networks between Strychni Semen and NSCLC were constructed via Cytoscape 3.9.1. Molecular docking detected interactions between the key components and the core targets. The core targets were validated via GEO datasets. 21 active components and 67 targets were identified, with 47 associated with NSCLC. The key active components were Stigmasterol, IcarideA, 2-Hydroxymethylanthraquinone, (+)-catechin, (2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)chroman-4-one, (S)-Stylopine, Brucine and Isobrucine. The core targets were PTGS2, NR3C1, ESR1, CASP3 and PRKACA. Molecular docking revealed that these compounds undergo strong binding affinity with the core genes. GEO database indicated that PTGS2 was the most promising core target. In addition, Strychni Semen's effects on NSCLC involved mainly the Calcium pathway, the Estrogen pathway, and the cGMP-PKG and cAMP pathways. This study visually demonstrated the mechanism of the therapeutic effect of Strychni Semen in NSCLC through multiple components, targets and pathways which provides a basis for clinical treatment and further experimental research.

马钱子治疗非小细胞肺癌机制的网络药理学与分子对接研究。
马钱子以其苦味和温性为特点,已被证实具有抗肿瘤的特性。但马钱子治疗非小细胞肺癌(NSCLC)的分子机制有待进一步研究。本研究旨在基于网络药理学和分子对接,探讨马钱子治疗NSCLC的分子机制。从中药数据库(TCMSP)中检索马钱子的有效成分和靶点,并辅以中药数据库和相关文献。nsclc相关靶点从GeneCards、OMIM和DisGenet数据库中检索。马钱子治疗NSCLC的交叉靶点通过在线平台获得。随后,通过String数据库构建蛋白质-蛋白质相互作用(PPI)网络,深入分析交叉靶点之间的相互关系。基因本体(GO)和京都基因与基因组百科全书(KEGG)途径分析通过metscape数据库进行。通过Cytoscape 3.9.1构建马钱子与NSCLC的交互网络。分子对接检测关键组分与核心靶点之间的相互作用。通过GEO数据集对核心目标进行验证。鉴定出21个有效成分和67个靶点,其中47个与NSCLC相关。主要活性成分为豆甾醇、伊卡迪亚、2-羟甲基蒽醌、(+)-儿茶素、(2R)-5,7-二羟基-2-(4-羟基苯基)铬-4-酮、(S)-苯乙烯平、马钱子碱和异马钱子碱。核心靶点为PTGS2、NR3C1、ESR1、CASP3和PRKACA。分子对接表明,这些化合物与核心基因具有较强的结合亲和力。GEO数据库显示,PTGS2是最有希望的核心靶点。此外,马钱子对NSCLC的作用主要涉及钙途径、雌激素途径以及cGMP-PKG和cAMP途径。本研究从多成分、多靶点、多途径直观地论证了马钱子对NSCLC的治疗作用机制,为临床治疗和进一步的实验研究提供了依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biological Procedures Online
Biological Procedures Online 生物-生化研究方法
CiteScore
10.50
自引率
0.00%
发文量
16
审稿时长
>12 weeks
期刊介绍: iological Procedures Online publishes articles that improve access to techniques and methods in the medical and biological sciences. We are also interested in short but important research discoveries, such as new animal disease models. Topics of interest include, but are not limited to: Reports of new research techniques and applications of existing techniques Technical analyses of research techniques and published reports Validity analyses of research methods and approaches to judging the validity of research reports Application of common research methods Reviews of existing techniques Novel/important product information Biological Procedures Online places emphasis on multidisciplinary approaches that integrate methodologies from medicine, biology, chemistry, imaging, engineering, bioinformatics, computer science, and systems analysis.
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