Meraz-Rodriguez Marco Antonio, Cháirez-Ramírez Manuel Humberto, de la Cruz-López Karen Griselda, González-Laredo Rubén Francisco, García-Carrancá Alejandro
Biomedical Cancer Research Unit, Institute for Biomedical Research, National Autonomous University of Mexico (UNAM) & National Cancer Institute, Mexico City, Mexico (Unidad de Investigación Biomédica en Cáncer, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México & Instituto Nacional de Cancerología, Ciudad de México, México).
PhD Program in Biochemical Sciences, Institute for Biomedical Research, National Autonomous University of Mexico (UNAM), Mexico City, Mexico (Programa de Doctorado en Ciencias Bioquímicas, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México (UNAM), Ciudad de México, México).
EXCLI J. 2025 Aug 1;24:957-991. doi: 10.17179/excli2025-8507. eCollection 2025.
G4-quadruplexes (G4s) are non-canonical structures of nucleic acids that develop in guanine rich regions of DNA and RNA. Due to their presence in oncogenic promoters and telomeres, G4s represent attractive targets in anticancer drug designs. G4s have also been the subject of recent research regarding their role as epigenetic modulators, supporting their participation in epigenetic processes that control gene expression. The development of small compounds that preferentially target G4s have led to a better understanding of how G4s control these mechanisms. Natural products have greatly contributed to the development of many successful examples of compounds with excellent anticancer activities. Therefore, it is important to investigate ligands targeting G4-quadruplexes in natural products such as dietary polyphenols and their derivatives. In this review, we provide an overview of the latest research on natural compounds, with especial emphasis on dietary polyphenols, as G4-quadruplex targeted ligands. We also discuss dietary polyphenols' structural chemistry that could facilitate their characterization as G4 ligands, highlighting their potential in the development of anticancer drugs. Finally, we explore polyphenols' potential mechanisms of action in regulating epigenetic machinery through G4 binding, thereby providing insights for the development of safe and effective therapeutical tools against cancer.
G4-四链体(G4s)是在DNA和RNA的富含鸟嘌呤区域形成的非经典核酸结构。由于它们存在于致癌启动子和端粒中,G4s成为抗癌药物设计中有吸引力的靶点。G4s也是近期关于其作为表观遗传调节剂作用研究的主题,这支持了它们参与控制基因表达的表观遗传过程。优先靶向G4s的小分子化合物的开发,使人们对G4s如何控制这些机制有了更好的理解。天然产物对许多具有优异抗癌活性的成功化合物的开发做出了巨大贡献。因此,研究天然产物如膳食多酚及其衍生物中靶向G4-四链体的配体很重要。在这篇综述中,我们概述了关于天然化合物的最新研究,特别强调膳食多酚作为靶向G4-四链体的配体。我们还讨论了膳食多酚的结构化学,这有助于将它们表征为G4配体,突出它们在抗癌药物开发中的潜力。最后,我们探讨了多酚通过G4结合调节表观遗传机制的潜在作用机制,从而为开发安全有效的抗癌治疗工具提供见解。