Anyanwu Margrate, Giannangeli Matteo, Fan Xing-Xing, Coghi Paolo, Ribaudo Giovanni, Gianoncelli Alessandra
Department of Molecular and Translational Medicine, University of Brescia, Brescia, Lombardy 25123, Italy.
Dr. Neher's Biophysics Laboratory for Innovative Drug Discovery, State Key Laboratory of Quality Research in Chinese Medicine, Macau University of Science and Technology, Taipa, Macau, SAR 999078, China.
ACS Med Chem Lett. 2024 Aug 21;15(9):1615-1619. doi: 10.1021/acsmedchemlett.4c00340. eCollection 2024 Sep 12.
G-Quadruplexes (G4s) are appealing targets for anticancer therapy because of their location in the genome and their role in regulating physiological and pathological processes. In this article, we report the characterization of the molecular interaction and selectivity of OAF89, a 9,10-disubstituted G4-binding anthracene derivative, with different DNA sequences. Advanced analytical methods, including mass spectrometry and nuclear magnetic resonance, were used to conduct the investigation, together with the use of docking and molecular dynamics. Eventually, the compound was tested to assess its bioactivity against lung cancer cell lines.
由于其在基因组中的位置以及在调节生理和病理过程中的作用,G-四链体(G4s)成为抗癌治疗的有吸引力的靶点。在本文中,我们报告了一种9,10-二取代的G4结合蒽衍生物OAF89与不同DNA序列的分子相互作用和选择性的表征。使用了包括质谱和核磁共振在内的先进分析方法进行研究,并结合对接和分子动力学方法。最终,对该化合物进行了测试,以评估其对肺癌细胞系的生物活性。