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Synthesis, characterization, antitumor potential, and investigation of mechanism of action of copper(ii) complexes with acylpyruvates as ligands: interactions with biomolecules and kinetic study

Authors :
Joksimović, Nenad
Petronijević, Jelena
Radisavljević, Snežana
Petrović, Biljana
Mihajlović, Kristina
Janković, Nenad
Milović, Emilija
Milivojević, Dušan
Ilić, Bojana
Đurić, Ana
Joksimović, Nenad
Petronijević, Jelena
Radisavljević, Snežana
Petrović, Biljana
Mihajlović, Kristina
Janković, Nenad
Milović, Emilija
Milivojević, Dušan
Ilić, Bojana
Đurić, Ana
Source :
RSC Advances
Publication Year :
2022

Abstract

Considering the urgency of finding a cure for vicious diseases such as tumors, we have synthesized and characterized a small series of new copper(ii) complexes with biologically important ligands such as acylpyruvate. In addition to this, we used another four copper(ii) complexes, with ligands of the same type to examine the antitumor potential. The antitumor potential of the copper(ii) complexes was examined on three tumor cell lines and one normal human cell line using the MTT assay. All seven tested complexes showed very good cytotoxic effects. Two copper complexes that showed the best antitumor potential were selected for further testing that showed the best potential for potential application in the future. The mechanism of activity of these complexes was examined in detail using tests such as cell cycle, ROS level, oxidative DNA damage, and proteins related to hypoxia analysis. In addition, we examined the binding abilities of these complexes with biomolecules (Guo, Ino, 5′-GMP, BSA, and DNA). The results showed that the tested compounds bind strongly to DNA molecules through intercalation. Also, it has been shown that the tested compounds adequately bind to the BSA molecule, which indicates an even greater potential for some future application of these compounds in clinical practice. © 2022 The Royal Society of Chemistry.

Details

Database :
OAIster
Journal :
RSC Advances
Notes :
RSC Advances
Publication Type :
Electronic Resource
Accession number :
edsoai.on1363261637
Document Type :
Electronic Resource