Banjan Bhavya, Koshy Abel John, Kalath Haritha, John Levin, Soman Sowmya, Raju Rajesh, Revikumar Amjesh
Centre for Integrative Omics Data Science (CIODS), Yenepoya (Deemed to Be University), Mangalore, Karnataka, 575018, India.
Kerala Genome Data Centre, Kerala Development and Innovation Strategic Council, Vazhuthacaud, Thiruvananthapuram, Kerala, 695014, India.
Mol Divers. 2024 Oct;28(5):3377-3391. doi: 10.1007/s11030-023-10768-7. Epub 2024 Mar 21.
Telomeric regions contain Guanine-rich sequences arranged in a planar manner and connected by Hoogsteen hydrogen bonds that can fold into G-quadruplex (G4) DNA structures, and can be stabilized by monovalent metal cations. The presence of G4 DNA holds significance in cancer-related processes, especially due to their regulatory potential at transcriptional and translational levels of oncogene and tumor suppressor genes. The objective of this current research is to explore the evolving realm of FDA-approved protein kinase inhibitors, with a specific emphasis on their capacity to stabilize the G4 DNA structures formed at the human telomeric regions. This involves investigating the possibility of repurposing FDA-approved protein kinase inhibitors as a novel approach for targeting multiple cancer types. In this context, we have selected 16 telomeric G4 DNA structures as targets and 71 FDA-approved small-molecule protein kinase inhibitors as ligands. To investigate their binding affinities, molecular docking of human telomeric G4 DNA with nuclear protein kinase inhibitors and their corresponding co-crystalized ligands were performed. We found that Ponatinib and Lapatinib interact with all the selected G4 targets, the binding free energy calculations, and molecular dynamic simulations confirm their binding efficacy and stability. Thus, it is hypothesized that Ponatinib and Lapatinib may stabilize human telomeric G4 DNA in addition to their ability to inhibit BCR-ABL and the other members of the EGFR family. As a result, we also hypothesize that the stabilization of G4 DNA might represent an additional underlying mechanism contributing to their efficacy in exerting anti-cancer effects.
端粒区域包含以平面方式排列并通过Hoogsteen氢键连接的富含鸟嘌呤的序列,这些序列可以折叠成G-四链体(G4)DNA结构,并可由单价金属阳离子稳定。G4 DNA的存在在癌症相关过程中具有重要意义,特别是由于它们在癌基因和肿瘤抑制基因的转录和翻译水平上的调控潜力。本研究的目的是探索FDA批准的蛋白激酶抑制剂的发展领域,特别强调它们稳定在人类端粒区域形成的G4 DNA结构的能力。这涉及研究将FDA批准的蛋白激酶抑制剂重新用于靶向多种癌症类型的新方法的可能性。在此背景下,我们选择了16种端粒G4 DNA结构作为靶点,71种FDA批准的小分子蛋白激酶抑制剂作为配体。为了研究它们的结合亲和力,我们对人类端粒G4 DNA与核蛋白激酶抑制剂及其相应的共结晶配体进行了分子对接。我们发现波纳替尼和拉帕替尼与所有选定的G4靶点相互作用,结合自由能计算和分子动力学模拟证实了它们的结合效力和稳定性。因此,据推测,波纳替尼和拉帕替尼除了能够抑制BCR-ABL和EGFR家族的其他成员外,还可能稳定人类端粒G4 DNA。因此,我们还推测G4 DNA的稳定可能代表了它们发挥抗癌作用的疗效的另一种潜在机制。