Lutimba Stuart, Saleem Baraya, Aleem Eiman, Mansour Mohammed A
Cancer Biology and Therapy Laboratory, School of Applied and Health Sciences, London South Bank University, London SE1 0AA, UK.
Biochemistry Division, Department of Chemistry, Faculty of Science, Tanta University, Tanta 31527, Egypt.
J Xenobiot. 2024 Dec 14;14(4):1962-1987. doi: 10.3390/jox14040105.
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.
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,据报道,这些蛋白质在不同疾病中存在失调,尤其是在癌症中,这些蛋白质促进肿瘤生长、侵袭、转移以及对传统疗法的耐药性。识别同时靶向VEGFR-2和c-Met的双重抑制剂已成为一种战略治疗方法,以克服临床环境中与单靶点疗法相关的局限性和耐药机制。通过分子动力学模拟和比较对接分析,我们测试了2016种美国食品药品监督管理局(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,恩他卡朋和替米沙坦分别是c-Met和VEGFR-2的强效和选择性抑制剂。有趣的是,氨苯蝶啶被确定为一种有前景的双重抑制剂,对这两种蛋白质均表现出特异性且显著的结合亲和力。分子动力学模拟揭示了所鉴定化合物与VEGFR-2(如Lys868、Asp1028、Asp1046)和c-Met(如Asp1204、His1202、Asp1222)催化结构域中的关键残基之间的关键相互作用,为它们的作用机制提供了见解。这些发现强调了氨苯蝶啶在靶向参与癌症进展、转移和患者不良预后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癌症多种通路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疗效,并测试它们克服耐药性和改善患者预后的能力。