Rocca Roberta, Moraca Federica, Costa Giosuè, Talarico Carmine, Ortuso Francesco, Da Ros Silvia, Nicoletto Giulia, Sissi Claudia, Alcaro Stefano, Artese Anna
Dipartimento di Scienze della Salute, Università "Magna Graecia" di Catanzaro, Campus "Salvatore Venuta", Viale Europa, 88100 Catanzaro, Italy.
Department of Pharmaceutical and Pharmacological Sciences, University of Padova, Via Marzolo 5, 35131 Padova, Italy.
ACS Med Chem Lett. 2018 Jul 10;9(8):848-853. doi: 10.1021/acsmedchemlett.8b00275. eCollection 2018 Aug 9.
In the last years, it has been shown that the DNA secondary structure known as G-quadruplex is also involved in the regulation of oncogenes transcription, such as , , , , , and . DNA G-quadruplexes, formed in the promoter region of these proto-oncogenes, are considered alternative anticancer targets since their stabilization causes a reduction of the related oncoprotein overexpression. In this study, a structure-based virtual screening toward the experimental DNA G-quadruplex structures of and was performed by using Glide for the docking analysis of a commercial library of approximately 693 000 compounds. The best hits were submitted to thermodynamic and biophysical studies, highlighting the effective stabilization of both G-quadruplex oncogene promoter structures for three -(4-piperidinylmethyl)amine derivatives, thus proposed as a new class of dual G-quadruplex binders.
在过去几年中,已表明被称为G-四链体的DNA二级结构也参与癌基因转录的调控,例如,,,,,和。在这些原癌基因启动子区域形成的DNA G-四链体被认为是替代性抗癌靶点,因为它们的稳定会导致相关癌蛋白过表达的减少。在本研究中,通过使用Glide对约693,000种化合物的商业文库进行对接分析,针对和的实验性DNA G-四链体结构进行了基于结构的虚拟筛选。最佳命中物被提交进行热力学和生物物理研究,突出了三种-(4-哌啶基甲基)胺衍生物对两种G-四链体癌基因启动子结构的有效稳定作用,因此被提议作为一类新的双G-四链体结合剂。