D-卡酮对非小细胞肺癌(NSCLC)的多靶点效应:基于网络药理学的研究

IF 3.3 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Rasha Irshad , Faiqah Batool , Nafis Raj , Shahid Karim , Huda Mohammed Alkreathy , Nikhat Manzoor , Mohammad Husain
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引用次数: 0

摘要

非小细胞肺癌(NSCLC)是一种具有高度异质性的复杂恶性肿瘤,约占所有肺癌病例的 85%。靶向疗法和免疫疗法的引入彻底改变了非小细胞肺癌的治疗格局;然而,要想提高治疗效果,还需要不断采用新的治疗模式。事实上,涉及天然产品的替代抗癌疗法因其显著的化学预防潜力而引起了临床医生和科学家的关注,这些天然产品通常显示出极小的毒性。D-香芹酮(D-carvone,CN)就是这样一种天然产品,它已显示出许多有希望的治疗效果,但其对 NSCLC 的疗效仍是个谜。本研究利用网络药理学研究和分子对接,结合体外验证,全面阐明了 D-香芹酮的潜在作用机制。不同的数据库共发现了 77 个 CN 的抗 NSCLC 靶点。我们利用Cytoscape(v3.9.0)软件构建了 "化合物-靶点-疾病 "网络,并对已确定的核心靶点进行了分析。进一步分析确定了 CN 的 5 个核心/枢纽靶点,包括 JAK2、ERK1、ESR1、GSK3B 和 HSP90AA1。分子对接表明,该化合物与这些核心靶点有很强的结合相互作用。基因本体和 KEGG 分析也验证了多种生物过程的参与。此外,通过流式细胞术、形态学评估和免疫印迹法检测,CN 能明显抑制 H1299 和 A549 细胞系的细胞增殖、克隆性和伤口愈合能力,同时促进细胞凋亡,其作用呈剂量依赖性。总之,本研究阐明了氯化萘对 NSCLC 的治疗作用,从而强调了氯化萘是一种有待进一步分析的候选药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Multi-targeted effects of D-carvone against Non-Small Cell Lung Cancer (NSCLC): A network pharmacology-based study

Multi-targeted effects of D-carvone against Non-Small Cell Lung Cancer (NSCLC): A network pharmacology-based study

Multi-targeted effects of D-carvone against Non-Small Cell Lung Cancer (NSCLC): A network pharmacology-based study

Non-small cell lung cancer (NSCLC) is a complex malignancy with a high degree of heterogeneity, representing approximately 85% of all lung cancer cases. The treatment landscape for NSCLC has been revolutionised by incorporating targeted and immunotherapies; however, novel therapeutic modalities are consistently needed to enhance the treatment outcomes. Indeed, alternative anti-cancer therapies involving natural products have drawn the attention of clinicians and scientists owing to their remarkable chemopreventive potential, often displaying minimal toxicity. D-carvone (CN) is one such natural product that has exhibited numerous promising therapeutic benefits, yet its efficacy against NSCLC remains enigmatic. In the present study, network pharmacological studies and molecular docking in conjunction with in-vitro validation were used to elucidate the underlying mechanism of action of CN comprehensively. Different databases revealed a total of 77 putative anti-NSCLC targets of CN. The identified core targets were utilised to construct a “Compound- Target- Disease” network by Cytoscape (v3.9.0). Further analysis identified 5 core/ hub targets of CN including JAK2, ERK1, ESR1, GSK3B and HSP90AA1. Molecular docking indicated a strong binding interaction of the compound with these core targets. Also, Gene Ontology and KEGG analysis validated the involvement of multiple biological processes. Additionally, CN significantly inhibited cell proliferation, clonogenicity, and wound healing potential while promoting apoptosis in a dose-dependent manner in H1299 and A549 cell lines as examined by flow cytometry, morphological assessment, and western blotting. In conclusion, this study delineates the therapeutic effects of CN on NSCLC, thus highlighting CN as a putative drug candidate for further analysis.

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来源期刊
CiteScore
6.80
自引率
2.60%
发文量
309
审稿时长
32 days
期刊介绍: Toxicology and Applied Pharmacology publishes original scientific research of relevance to animals or humans pertaining to the action of chemicals, drugs, or chemically-defined natural products. Regular articles address mechanistic approaches to physiological, pharmacologic, biochemical, cellular, or molecular understanding of toxicologic/pathologic lesions and to methods used to describe these responses. Safety Science articles address outstanding state-of-the-art preclinical and human translational characterization of drug and chemical safety employing cutting-edge science. Highly significant Regulatory Safety Science articles will also be considered in this category. Papers concerned with alternatives to the use of experimental animals are encouraged. Short articles report on high impact studies of broad interest to readers of TAAP that would benefit from rapid publication. These articles should contain no more than a combined total of four figures and tables. Authors should include in their cover letter the justification for consideration of their manuscript as a short article.
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