Exploring the interaction of Curaxin CBL0137 with G-Quadruplex DNA oligomers

Curaxins and especially the second-generation derivative curaxin CBL0137 have important antitumor activities in multiple cancers such as glioblastoma, melanoma and others. Although most of the authors suggest that their mechanism of action comes from the activation of p53 and inactivation of NF-kB b...

Descripción completa

Detalles Bibliográficos
Autores: Dallavalle, Sabrina, Mattio, Luce M., Artali, Roberto, Musso, Loana, Aviñó Andrés, Anna, Fàbrega i Claveria, Ma. Carme, Eritja i Casadellà, Ramon, Gargallo Gómez, Raimundo, Mazzini, Stefania
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2021
País:España
Institución:Universidad de Barcelona
Repositorio:Dipòsit Digital de la UB
OAI Identifier:oai:diposit.ub.edu:2445/178494
Acceso en línea:https://hdl.handle.net/2445/178494
Access Level:acceso abierto
Palabra clave:G-estructures
Espectroscòpia de ressonància magnètica nuclear
Oligòmers
G-structures
Nuclear magnetic resonance spectroscopy
Oligomers
Descripción
Sumario:Curaxins and especially the second-generation derivative curaxin CBL0137 have important antitumor activities in multiple cancers such as glioblastoma, melanoma and others. Although most of the authors suggest that their mechanism of action comes from the activation of p53 and inactivation of NF-kB by targeting FACT, there is evidence supporting the involvement of DNA binding in their antitumor activity. In this work, the DNA binding properties of curaxin CBL0137 with model quadruplex DNA oligomers were studied by 1H NMR, CD, fluorescence and molecular modeling. We provided molecular details of the interaction of curaxin with two G-quadruplex structures, the single repeat of human telomere d(TTAGGGT)4 and the c-myc promoter Pu22 sequence. We also performed 1H and 31P NMR experiments were also performed in order to investigate the interaction with duplex DNA models. Our data support the hypothesis that the interaction of curaxin with G-quadruplex may provide a novel insight into the DNA-binding properties of CBL0137, and it will be helpful for the design of novel selective DNA-targeting curaxin analogues.