| Literature DB >> 30826512 |
Tiago Moreira1, Rita Francisco1, Elisabeta Comsa2, Sophie Duban-Deweer3, Valérie Labas4, Ana-Paula Teixeira-Gomes4, Lucie Combes-Soia4, Fernanda Marques5, António Matos6, Audrey Favrelle7, Cyril Rousseau8, Philippe Zinck7, Pierre Falson2, M Helena Garcia9, Ana Preto10, Andreia Valente11.
Abstract
In this work, we aimed to understand the biological activity and the mechanism of action of three polymer-'ruthenium-cyclopentadienyl' conjugates (RuPMC) and a low molecular weight parental compound (Ru1) in cancer cells. Several biological assays were performed in ovarian (A2780) and breast (MCF7, MDA-MB-231) human cancer derived cell lines as well as in A2780cis, a cisplatin resistant cancer cell line. Our results show that all compounds have high activity towards cancer cells with low IC50 values in the micromolar range. We observed that all Ru-PMC compounds are mainly found inside the cells, in contrast with the parental low molecular weight compound Ru1 that was mainly found at the membrane. All compounds induced mitochondrial alterations. PMC3 and Ru1 caused F-actin cytoskeleton morphology changes and reduced the clonogenic ability of the cells. The conjugate PMC3 induced apoptosis at low concentrations comparing to cisplatin and could overcame the platinum resistance of A2780cis cancer cells. A proteomic analysis showed that these compounds induce alterations in several cellular proteins which are related to the phenotypic disorders induced by them. Our results suggest that PMC3 is foreseen as a lead candidate to future studies and acting through a different mechanism of action than cisplatin. Here we established the potential of these Ru compounds as new metallodrugs for cancer chemotherapy.Entities:
Keywords: Cytoskeleton; Polymer-metal conjugates; Proteomic analysis; Ruthenium organometallic compounds
Mesh:
Substances:
Year: 2019 PMID: 30826512 DOI: 10.1016/j.ejmech.2019.02.061
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514