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基于网络药理学和分子对接技术探究黄连-生姜对抗结肠癌的活性成分及作用机制。

Exploring active ingredients and mechanisms of Coptidis Rhizoma-ginger against colon cancer using network pharmacology and molecular docking.

机构信息

Institute of Systems Engineering and Collaborative Laboratory for Intelligent Science and Systems, Macau University of Science and Technology, Taipa, Macao, China.

Faculty of Information Technology, Macau University of Science and Technology, Taipa, Macao, China.

出版信息

Technol Health Care. 2024;32(S1):523-542. doi: 10.3233/THC-248046.

Abstract

BACKGROUND

Colon cancer is the most prevalent and rapidly increasing malignancy globally. It has been suggested that some of the ingredients in the herb pair of Coptidis Rhizoma and ginger (Zingiber officinale), a traditional Chinese medicine, have potential anti-colon cancer properties.

OBJECTIVE

This study aimed to investigate the molecular mechanisms underlying the effects of the Coptidis Rhizoma-ginger herb pair in treating colon cancer, using an integrated approach combining network pharmacology and molecular docking.

METHODS

The ingredients of the herb pair Coptidis Rhizoma-ginger, along with their corresponding protein targets, were obtained from the Traditional Chinese Medicine System Pharmacology and Swiss Target Prediction databases. Target genes associated with colon cancer were retrieved from the GeneCards and OMIM databases. Then, the protein targets of the active ingredients in the herb pair were identified, and the disease-related overlapping targets were determined using the Venn online tool. The protein-protein interaction (PPI) network was constructed using STRING database and analyzed using Cytoscape 3.9.1 to identify key targets. Then, a compound-target-disease-pathway network map was constructed. The intersecting target genes were subjected to Gene Ontology (GO) enrichment and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses for colon cancer treatment. Molecular docking was performed using the Molecular Operating Environment (MOE) software to predict the binding affinity between the key targets and active compounds.

RESULTS

Besides 1922 disease-related targets, 630 targets associated with 20 potential active compounds of the herb pair Coptidis Rhizoma-ginger were collected. Of these, 229 intersection targets were obtained. Forty key targets, including STAT3, Akt1, SRC, and HSP90AA1, were further analyzed using the ClueGO plugin in Cytoscape. These targets are involved in biological processes such as miRNA-mediated gene silencing, phosphatidylinositol 3-kinase (PI3K) signaling, and telomerase activity. KEGG enrichment analysis showed that PI3K-Akt and hypoxia-inducible factor 1 (HIF-1) signaling pathways were closely related to colon cancer prevention by the herb pair Coptidis Rhizoma-ginger. Ten genes (Akt1, TP53, STAT3, SRC, HSP90AA1, JAK2, CASP3, PTGS2, BCl2, and ESR1) were identified as key genes for validation through molecular docking simulation.

CONCLUSIONS

This study demonstrated that the herb pair Coptidis Rhizoma-ginger exerted preventive effects against colon cancer by targeting multiple genes, utilizing various active compounds, and modulating multiple pathways. These findings might provide the basis for further investigations into the molecular mechanisms underlying the therapeutic effects of Coptidis Rhizoma-ginger in colon cancer treatment, potentially leading to the development of novel drugs for combating this disease.

摘要

背景

结肠癌是全球最普遍且发病率增长最快的恶性肿瘤之一。有研究表明,中药黄连和生姜(Zingiber officinale)药对中的一些成分可能具有抗结肠癌的特性。

目的

本研究旨在采用网络药理学和分子对接相结合的综合方法,探讨黄连-生姜药对对结肠癌的作用机制。

方法

从中药系统药理学数据库和瑞士靶向预测数据库中获取黄连-生姜药对的成分及其相应的蛋白靶标。从 GeneCards 和 OMIM 数据库中检索与结肠癌相关的靶基因。然后,使用 Venn 在线工具确定药对中活性成分的靶标,并确定疾病相关的重叠靶标。使用 STRING 数据库构建蛋白质-蛋白质相互作用(PPI)网络,并使用 Cytoscape 3.9.1 进行分析,以确定关键靶标。然后构建化合物-靶标-疾病-通路网络图。对交集靶基因进行基因本体论(GO)富集和京都基因与基因组百科全书(KEGG)通路分析,以探讨其在结肠癌治疗中的作用机制。使用分子操作环境(MOE)软件进行分子对接,预测关键靶标与活性化合物的结合亲和力。

结果

除了 1922 个疾病相关靶标外,还收集了黄连-生姜药对 20 种潜在活性化合物相关的 630 个靶标。其中,获得了 229 个交集靶标。使用 Cytoscape 中的 ClueGO 插件对 40 个关键靶标(包括 STAT3、Akt1、SRC 和 HSP90AA1)进行了进一步分析。这些靶标参与 miRNA 介导的基因沉默、磷脂酰肌醇 3-激酶(PI3K)信号和端粒酶活性等生物学过程。KEGG 富集分析表明,PI3K-Akt 和缺氧诱导因子 1(HIF-1)信号通路与黄连-生姜药对预防结肠癌密切相关。通过分子对接模拟,鉴定出 10 个关键基因(Akt1、TP53、STAT3、SRC、HSP90AA1、JAK2、CASP3、PTGS2、BCL2 和 ESR1)进行验证。

结论

本研究表明,黄连-生姜药对通过作用于多个基因、利用多种活性化合物、调节多条通路,对结肠癌发挥预防作用。这些发现可能为进一步研究黄连-生姜在结肠癌治疗中的治疗作用机制提供依据,从而为治疗这种疾病开发新的药物提供可能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe38/11191530/1e63c816addf/thc-32-thc248046-g001.jpg

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