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Polymer "ruthenium-cyclopentadienyl" conjugates - New emerging anti-cancer drugs. | LitMetric

AI Article Synopsis

  • The study investigated the biological effects and mechanisms of three polymer-'ruthenium-cyclopentadienyl' conjugates (RuPMC) and a parental compound (Ru1) on human cancer cells, particularly focusing on ovarian and breast cancer lines.
  • All tested compounds demonstrated significant anti-cancer activity with low effective concentrations, with RuPMC compounds mainly localizing within cells, unlike Ru1, which stayed at the membrane.
  • PMC3 showed potential in inducing apoptosis at lower concentrations than the standard drug cisplatin, highlighting its effectiveness against cisplatin-resistant cancer cells and suggesting it could be a promising candidate for future cancer treatments.

Article 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 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.

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Source
http://dx.doi.org/10.1016/j.ejmech.2019.02.061DOI Listing

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