Publication Type Journal Article
Title New copper(I) and heteronuclear copper(I)-ruthenium(II) complexes: Synthesis, structural characterization and cytotoxicity
Authors Joao Lopes David Alves Tânia S. Morais Paulo J. Costa M.Fatima M.Piedade Fernanda M. Marques Maria J. Villa de Brito M. Helena Garcia
Groups BIOIN BioMol
Journal JOURNAL OF INORGANIC BIOCHEMISTRY
Year 2017
Month April
Volume 169
Number
Pages 68-78
Abstract A new family of copper(I) complexes of general formula [Cu(dppe)(NN)](+) have been synthesized and fully characterized, with dppe = 1.2-bis(diphenylphosphino)ethane and NN representing several bidentate heteroaromatic ligands: 22 -bipy = 2.2 -bipyridine (1), Me(2)bpy = 4.4 -dimethyl-2,2 -bipyridine (2), dpytz = 3-(2-pyridyl)-5,6-diphenyl-1,2,4-triazine (3), dpp = 2.3-bis(2-pyridyl)pyrazine (4), and the metallaligand [Ru(eta(5)-C5H5)(PPh3)(dpp)](+) (5), yielding the bimetallic copper(l)-ruthenium(II) complex [Cu( dppe)( mu-dpp)Ru(eta(5)-O5H5)(PPh3)](2+) (6). The single crystal structures of complexes (2) and (4) were determined by Xray diffraction studies. All the complexes exhibit high cytotoxicity against the human cancer cells A2780 and MCF7 with IC50 values far lower than those found for the antitumor drug cisplatin in the same cell lines and even surpassing cisplatin resistance in the A2780cisR cells. They display IC50 values on the human embryonic kidney HEK293 non-tumoral cells of the same order of magnitude as those found for the tumoral cells. In the ovarian cells the compounds induce rapid production of reactive oxygen species (ROS) probably through mitochondrial pathways. According to the results reported here, these compounds can be considered as prospective antitumoral agents that deserve further evaluation. (C) 2017 Elsevier Inc. All rights reserved.
DOI http://dx.doi.org/10.1016/jjinorgbio.2017.01.007
ISBN
Publisher ELSEVIER SCIENCE INC
Book Title
ISSN 0162-0134
EISSN 1873-3344
Conference Name
Bibtex ID ISI:000395849500008
Observations
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