Please use this identifier to cite or link to this item: http://www.repositorio.ufop.br/jspui/handle/123456789/17874
Title: Cytotoxic activity of Ru(II)/DPEPhos/N,S-mercapto complexes (DPEPhos = bis-[(2-diphenylphosphino)phenyl]ether).
Authors: Grawe, Gregory Ferreira
Oliveira, Katia Mara de
Leite, Celisnolia Morais
Oliveira, Tamires Donizeth de
Costa, Analu Rocha
Moraes, Carlos André Ferreira
Araujo Neto, João Honorato de
Cominetti, Márcia Regina
Castellano, Eduardo Ernesto
Correa, Rodrigo de Souza
Machado, Sérgio de Paula
Batista, Alzir Azevedo
Keywords: Ruthenium complexes
N,S-mercapto ligands
Cytotoxicity
Breast cancer
Lung cancer
Issue Date: 2023
Citation: GRAWE, G. F. et al. Cytotoxic activity of Ru(II)/DPEPhos/N,S-mercapto complexes (DPEPhos = bis-[(2-diphenylphosphino)phenyl]ether). Journal of Inorganic Biochemistry, v. 244, artigo 112204, 2023. Disponível em: <https://www.sciencedirect.com/science/article/pii/S0162013423000867>. Acesso em: 01 ago. 2023.
Abstract: We report here on three new ruthenium(II) complexes, [Ru(DPEPhos)(mtz)(bipy)]PF6 (Ru1), [Ru(DPEPhos) (mmi)(bipy)]PF6 (Ru2) and [Ru(DPEPhos)(dmp)(bipy)]PF6 (Ru3). DPEPhos = bis-[(2-diphenylphosphino) phenyl]ether, mtz = 2-mercapto-2-thiazoline, mmi = 2-mercapto-1-methylimidazole, dmp = 4,6-diamino-2- mercaptopyrimidine and bipy = 2,2′ -bipyridine. The compounds were characterized by several spectroscopic techniques, and the molecular structure of Ru1 complex was determined by single-crystal X-ray diffraction. The cytotoxicity of Ru1 – Ru3 complexes were tested against the A549 (human lung) and the MDA-MB-231 (human breast) cancer cell lines and against MRC-5 (non-tumor lung) and MCF-10A (non-tumor breast) cell lines through the MTT assay. All three complexes are cytotoxic against the cell lines studied, with IC50 values lower than those found for the cisplatin. Among them, the Ru2 complex has shown the best selectivity against MDA-MB-231 cancer cell lines, with an IC50 value 12 times lower than that on MCF-10A. The complex Ru2 was capable to induce changes in MDA-MB-231 cells morphology, with loss of cellular adhesion, inhibited colony formation and induce an accumulation of cells at the sub-G1 phase, with an increase in S-phase and decrease of cells at G2 phase. Viscosity, electrochemical and Hoechst 33258 displacement experiments for Ru1 – Ru3 complexes with calf thymus DNA (CT-DNA) showed an electrostatic and groove binding mode of interaction. Additionally, the complexes interact with the protein Human Serum Albumin (HSA) by static mechanism. The negative values for ΔH and ΔS indicate that van der Waals forces and hydrogen bonding may occurs between the complexes and HSA. Therefore, this class of complexes are promising anticancer candidates and may be selected to further detailed studies.
URI: http://www.repositorio.ufop.br/jspui/handle/123456789/17874
metadata.dc.identifier.uri2: https://www.sciencedirect.com/science/article/pii/S0162013423000867
metadata.dc.identifier.doi: https://doi.org/10.1016/j.jinorgbio.2023.112204
ISSN: 0162-0134
Appears in Collections:DEQUI - Artigos publicados em periódicos

Files in This Item:
File Description SizeFormat 
ARTIGO_CytotoxicActivityRu.pdf
  Restricted Access
6,26 MBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.