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Anticancer Water‐Soluble Organoruthenium Complexes: Synthesis and Preclinical Evaluation
The synthesis, characterisation, and evaluation of the in vitro cytotoxicity of five maleonitriledithiolate‐based ruthenium metal complexes bearing various phosphine ligands towards two ovarian cancer cell lines (A2780 and A2780cisR), one non‐small‐cell lung cancer cell line (H460) and one normal pr...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545474/ https://www.ncbi.nlm.nih.gov/pubmed/35838006 http://dx.doi.org/10.1002/cbic.202200259 |
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author | Azmanova, Maria Rafols, Laia Cooper, Patricia A. Seaton, Colin C. Shnyder, Steven D. Pitto‐Barry, Anaïs |
author_facet | Azmanova, Maria Rafols, Laia Cooper, Patricia A. Seaton, Colin C. Shnyder, Steven D. Pitto‐Barry, Anaïs |
author_sort | Azmanova, Maria |
collection | PubMed |
description | The synthesis, characterisation, and evaluation of the in vitro cytotoxicity of five maleonitriledithiolate‐based ruthenium metal complexes bearing various phosphine ligands towards two ovarian cancer cell lines (A2780 and A2780cisR), one non‐small‐cell lung cancer cell line (H460) and one normal prostate cell line (PNT2) are presented herein. These 18‐electron complexes were designed with four water‐soluble phosphine ligands to increase the water‐solubility character of the corresponding electron‐deficient ruthenium complex which showed great in vitro promises, and triphenylphosphine for comparison. The complexes with triphenylphosphine‐3,3′,3′′‐trisulfonic acid and triphenylphosphine present similar cytotoxicity compared to the 16‐electron precursor, with equal cytotoxicity to both A2780 and A2780cisR. Hints at the mechanism of action suggest an apoptotic pathway based on reactive oxygen species (ROS) production. No toxicity was observed in preliminary in vivo pilot studies for these two complexes in subcutaneous A2780 and A2780cisR xenograft models, with some evidence of tumour growth delay. |
format | Online Article Text |
id | pubmed-9545474 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95454742022-10-14 Anticancer Water‐Soluble Organoruthenium Complexes: Synthesis and Preclinical Evaluation Azmanova, Maria Rafols, Laia Cooper, Patricia A. Seaton, Colin C. Shnyder, Steven D. Pitto‐Barry, Anaïs Chembiochem Research Articles The synthesis, characterisation, and evaluation of the in vitro cytotoxicity of five maleonitriledithiolate‐based ruthenium metal complexes bearing various phosphine ligands towards two ovarian cancer cell lines (A2780 and A2780cisR), one non‐small‐cell lung cancer cell line (H460) and one normal prostate cell line (PNT2) are presented herein. These 18‐electron complexes were designed with four water‐soluble phosphine ligands to increase the water‐solubility character of the corresponding electron‐deficient ruthenium complex which showed great in vitro promises, and triphenylphosphine for comparison. The complexes with triphenylphosphine‐3,3′,3′′‐trisulfonic acid and triphenylphosphine present similar cytotoxicity compared to the 16‐electron precursor, with equal cytotoxicity to both A2780 and A2780cisR. Hints at the mechanism of action suggest an apoptotic pathway based on reactive oxygen species (ROS) production. No toxicity was observed in preliminary in vivo pilot studies for these two complexes in subcutaneous A2780 and A2780cisR xenograft models, with some evidence of tumour growth delay. John Wiley and Sons Inc. 2022-08-03 2022-09-16 /pmc/articles/PMC9545474/ /pubmed/35838006 http://dx.doi.org/10.1002/cbic.202200259 Text en © 2022 The Authors. ChemBioChem published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Azmanova, Maria Rafols, Laia Cooper, Patricia A. Seaton, Colin C. Shnyder, Steven D. Pitto‐Barry, Anaïs Anticancer Water‐Soluble Organoruthenium Complexes: Synthesis and Preclinical Evaluation |
title | Anticancer Water‐Soluble Organoruthenium Complexes: Synthesis and Preclinical Evaluation |
title_full | Anticancer Water‐Soluble Organoruthenium Complexes: Synthesis and Preclinical Evaluation |
title_fullStr | Anticancer Water‐Soluble Organoruthenium Complexes: Synthesis and Preclinical Evaluation |
title_full_unstemmed | Anticancer Water‐Soluble Organoruthenium Complexes: Synthesis and Preclinical Evaluation |
title_short | Anticancer Water‐Soluble Organoruthenium Complexes: Synthesis and Preclinical Evaluation |
title_sort | anticancer water‐soluble organoruthenium complexes: synthesis and preclinical evaluation |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545474/ https://www.ncbi.nlm.nih.gov/pubmed/35838006 http://dx.doi.org/10.1002/cbic.202200259 |
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