Centro de Química Estrutural, Faculdade de Ciências da Universidade de Lisboa, Campo Grande, 1749-016, Lisboa, Portugal; Centre of Molecular and Environmental Biology (CBMA), Department of Biology, University of Minho, Portugal. Campus de Gualtar, Braga, 4710-057, Portugal.
Drug Resistance & Membrane Proteins Team, Molecular Microbiology and Structural Biochemistry Laboratory, CNRS-UCBL1 UMR 5086, IBCP, 69367, Lyon, France.
Eur J Med Chem. 2019 Apr 15;168:373-384. doi: 10.1016/j.ejmech.2019.02.061. Epub 2019 Feb 25.
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 IC 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.
在这项工作中,我们旨在了解三种聚合物-“钌-环戊二烯基”缀合物(RuPMC)和一种低分子量母体化合物(Ru1)在癌细胞中的生物学活性和作用机制。在卵巢(A2780)和乳腺癌(MCF7、MDA-MB-231)人癌细胞系以及顺铂耐药癌细胞系 A2780cis 中进行了多项生物学测定。我们的结果表明,所有化合物对癌细胞均具有高活性,IC 值在微摩尔范围内较低。我们观察到所有 Ru-PMC 化合物主要存在于细胞内,而母体低分子量化合物 Ru1 主要存在于细胞膜上。所有化合物均诱导线粒体改变。PMC3 和 Ru1 引起 F-肌动蛋白细胞骨架形态变化,并降低细胞的集落形成能力。与顺铂相比,低浓度的缀合物 PMC3 诱导细胞凋亡,并能克服 A2780cis 癌细胞的铂耐药性。蛋白质组学分析表明,这些化合物诱导几种与它们诱导的表型障碍相关的细胞蛋白发生改变。我们的结果表明,PMC3 有望成为未来研究的候选药物,其作用机制与顺铂不同。在这里,我们确定了这些 Ru 化合物作为癌症化疗新金属药物的潜力。