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ROS1激酶抑制作用的新设想:通过虚拟筛选和分子动力学模拟鉴定用于癌症治疗的 repurposed 药物。

ROS1 kinase inhibition reimagined: identifying repurposed drug via virtual screening and molecular dynamics simulations for cancer therapeutics.

作者信息

Alrouji Mohammed, Yasmin Sabina, Alhumaydhi Fahad A, Sharaf Sharaf E, Shahwan Moyad, Shamsi Anas

机构信息

Department of Medical Laboratories, College of Applied Medical Sciences, Shaqra University, Shaqra, Saudi Arabia.

Department of Pharmaceutical Chemistry, College of Pharmacy, King Khalid University, Abha, Saudi Arabia.

出版信息

Front Chem. 2024 Jul 29;12:1392650. doi: 10.3389/fchem.2024.1392650. eCollection 2024.

Abstract

Precision medicine has revolutionized modern cancer therapeutic management by targeting specific molecular aberrations responsible for the onset and progression of tumorigenesis. ROS proto-oncogene 1 (ROS1) is a receptor tyrosine kinase (RTK) that can induce tumorigenesis through various signaling pathways, such as cell proliferation, survival, migration, and metastasis. It has emerged as a promising therapeutic target in various cancer types. However, there is very limited availability of specific ROS1 inhibitors for therapeutic purposes. Exploring repurposed drugs for rapid and effective treatment is a useful approach. In this study, we utilized an integrated approach of virtual screening and molecular dynamics (MD) simulations of repurposing existing drugs for ROS1 kinase inhibition. Using a curated library of 3648 FDA-approved drugs, virtual screening identified drugs capable of binding to ROS1 kinase domain. The results unveil two hits, Midostaurin and Alectinib with favorable binding profiles and stable interactions with the active site residues of ROS1. These hits were subjected to stability assessment through all-atom MD simulations for 200 ns. MD results showed that Midostaurin and Alectinib were stable with ROS1. Taken together, the study showed a rational framework for the selection of repurposed Midostaurin and Alectinib with ROS1 inhibitory potential for therapeutic management after further validation.

摘要

精准医学通过针对导致肿瘤发生和进展的特定分子异常,彻底改变了现代癌症治疗管理。ROS原癌基因1(ROS1)是一种受体酪氨酸激酶(RTK),可通过多种信号通路诱导肿瘤发生,如细胞增殖、存活、迁移和转移。它已成为各种癌症类型中有前景的治疗靶点。然而,用于治疗目的的特异性ROS1抑制剂的可用性非常有限。探索重新利用的药物进行快速有效治疗是一种有用的方法。在本研究中,我们采用了虚拟筛选和分子动力学(MD)模拟的综合方法,重新利用现有药物抑制ROS1激酶。使用一个由3648种FDA批准药物组成的精选库,虚拟筛选确定了能够与ROS1激酶结构域结合的药物。结果揭示了两个命中药物,米哚妥林和阿来替尼,它们具有良好的结合模式,并与ROS1的活性位点残基有稳定的相互作用。通过200纳秒的全原子MD模拟对这些命中药物进行稳定性评估。MD结果表明米哚妥林和阿来替尼与ROS1稳定结合。综上所述,该研究展示了一个合理的框架,用于选择具有ROS1抑制潜力的重新利用的米哚妥林和阿来替尼,以便在进一步验证后用于治疗管理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ae5/11317403/646db8f5713c/fchem-12-1392650-g001.jpg

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