In Silico Analysis of Triamterene as a Potential Dual Inhibitor of VEGFR-2 and c-Met Receptors.

IF 6.8 Q1 TOXICOLOGY Journal of Xenobiotics Pub Date : 2024-12-14 DOI:10.3390/jox14040105
Stuart Lutimba, Baraya Saleem, Eiman Aleem, Mohammed A Mansour
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Abstract

The vascular endothelial growth factor receptor 2 (VEGFR2) and the hepatocyte growth factor receptor (C-Met) are critical receptors for signaling pathways controlling crucial cellular processes such as cell growth, angiogenesis and tissue regeneration. However, dysregulation of these proteins has been reported in different diseases, particularly cancer, where these proteins promote tumour growth, invasiveness, metastasis and resistance to conventional therapies. The identification of dual inhibitors targeting both VEGFR-2 and c-Met has emerged as a strategic therapeutic approach to overcome the limitations and resistance mechanisms associated with single-target therapies in clinical settings. Through molecular dynamics simulations and comparative docking analysis, we tested the inhibitory potential of 2,016 Food and Drug Administration (FDA)-approved drugs targeting VEGFR-2 and/or c-Met receptors. The results revealed that entacapone and telmisartan are potent and selective inhibitors for c-Met and VEGFR-2, respectively. Interestingly, triamterene was identified as a promising dual inhibitor, demonstrating specific and significant binding affinity to both proteins. Molecular dynamics simulations revealed key interactions between the identified compounds and critical residues in the catalytic domains of both VEGFR-2 (e.g., Lys868, Asp1028, Asp1046) and c-Met (e.g., Asp1204, His1202, Asp1222), providing insights into their mechanism of action. These findings underscore the therapeutic potential of triamterene in targeting multiple signaling pathways involved in cancer progression, metastasis and poor prognosis in patients. Our study provides a foundational framework for the development of novel anticancer compounds able to target multiple pathways in cancer. Further preclinical and clinical investigations are needed to validate the efficacy of these compounds in clinical settings and to test their ability to overcome resistance and improve patient outcome.

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三胺萜烯作为VEGFR-2和c-Met受体潜在双重抑制剂的硅分析。
血管内皮生长因子受体2 (VEGFR2)和肝细胞生长因子受体(C-Met)是控制细胞生长、血管生成和组织再生等关键细胞过程的信号通路的关键受体。然而,这些蛋白的失调已经在不同的疾病中被报道,特别是在癌症中,这些蛋白促进肿瘤生长、侵袭性、转移和对常规疗法的抵抗。针对VEGFR-2和c-Met的双重抑制剂的鉴定已经成为克服临床环境中与单靶点治疗相关的局限性和耐药机制的一种战略性治疗方法。通过分子动力学模拟和比较对接分析,我们测试了2016种FDA批准的靶向VEGFR-2和/或c-Met受体的药物的抑制潜力。结果显示恩他卡彭和替米沙坦分别是c-Met和VEGFR-2的有效和选择性抑制剂。有趣的是,triamterene被认为是一种有前景的双重抑制剂,对这两种蛋白都具有特异性和显著的结合亲和力。分子动力学模拟揭示了所鉴定的化合物与VEGFR-2(例如,Lys868, Asp1028, Asp1046)和c-Met(例如,Asp1204, His1202, Asp1222)催化域中关键残基之间的关键相互作用,从而深入了解它们的作用机制。这些发现强调了曲氨蝶烯在针对癌症进展、转移和预后不良患者的多种信号通路方面的治疗潜力。我们的研究为开发能够靶向多种癌症途径的新型抗癌化合物提供了基础框架。需要进一步的临床前和临床研究来验证这些化合物在临床环境中的有效性,并测试它们克服耐药性和改善患者预后的能力。
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来源期刊
CiteScore
5.30
自引率
1.70%
发文量
21
审稿时长
10 weeks
期刊介绍: The Journal of Xenobiotics publishes original studies concerning the beneficial (pharmacology) and detrimental effects (toxicology) of xenobiotics in all organisms. A xenobiotic (“stranger to life”) is defined as a chemical that is not usually found at significant concentrations or expected to reside for long periods in organisms. In addition to man-made chemicals, natural products could also be of interest if they have potent biological properties, special medicinal properties or that a given organism is at risk of exposure in the environment. Topics dealing with abiotic- and biotic-based transformations in various media (xenobiochemistry) and environmental toxicology are also of interest. Areas of interests include the identification of key physical and chemical properties of molecules that predict biological effects and persistence in the environment; the molecular mode of action of xenobiotics; biochemical and physiological interactions leading to change in organism health; pathophysiological interactions of natural and synthetic chemicals; development of biochemical indicators including new “-omics” approaches to identify biomarkers of exposure or effects for xenobiotics.
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