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An Organometallic Gold(I) Bis‐N‐Heterocyclic Carbene Complex with Multimodal Activity in Ovarian Cancer Cells
The organometallic Au(I) bis‐N‐heterocyclic carbene complex [Au(9‐methylcaffeine‐8‐ylidene)(2)](+) (AuTMX(2)) was previously shown to selectively and potently stabilise telomeric DNA G‐quadruplex (G4) structures. This study sheds light on the molecular reactivity and mode of action of AuTMX(2) in th...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756355/ https://www.ncbi.nlm.nih.gov/pubmed/32902006 http://dx.doi.org/10.1002/chem.202003495 |
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author | Meier‐Menches, Samuel M. Neuditschko, Benjamin Zappe, Katja Schaier, Martin Gerner, Marlene C. Schmetterer, Klaus G. Del Favero, Giorgia Bonsignore, Riccardo Cichna‐Markl, Margit Koellensperger, Gunda Casini, Angela Gerner, Christopher |
author_facet | Meier‐Menches, Samuel M. Neuditschko, Benjamin Zappe, Katja Schaier, Martin Gerner, Marlene C. Schmetterer, Klaus G. Del Favero, Giorgia Bonsignore, Riccardo Cichna‐Markl, Margit Koellensperger, Gunda Casini, Angela Gerner, Christopher |
author_sort | Meier‐Menches, Samuel M. |
collection | PubMed |
description | The organometallic Au(I) bis‐N‐heterocyclic carbene complex [Au(9‐methylcaffeine‐8‐ylidene)(2)](+) (AuTMX(2)) was previously shown to selectively and potently stabilise telomeric DNA G‐quadruplex (G4) structures. This study sheds light on the molecular reactivity and mode of action of AuTMX(2) in the cellular context using mass spectrometry‐based methods, including shotgun proteomics in A2780 ovarian cancer cells. In contrast to other metal‐based anticancer agents, this organogold compound is less prone to form coordinative bonds with biological nucleophiles and is expected to exert its drug effects mainly by non‐covalent interactions. Global protein expression changes of treated cancer cells revealed a multimodal mode of action of AuTMX(2) by alterations in the nucleolus, telomeres, actin stress‐fibres and stress‐responses, which were further supported by pharmacological assays, fluorescence microscopy and cellular accumulation experiments. Proteomic data are available via ProteomeXchange with identifier PXD020560. |
format | Online Article Text |
id | pubmed-7756355 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77563552020-12-28 An Organometallic Gold(I) Bis‐N‐Heterocyclic Carbene Complex with Multimodal Activity in Ovarian Cancer Cells Meier‐Menches, Samuel M. Neuditschko, Benjamin Zappe, Katja Schaier, Martin Gerner, Marlene C. Schmetterer, Klaus G. Del Favero, Giorgia Bonsignore, Riccardo Cichna‐Markl, Margit Koellensperger, Gunda Casini, Angela Gerner, Christopher Chemistry Full Papers The organometallic Au(I) bis‐N‐heterocyclic carbene complex [Au(9‐methylcaffeine‐8‐ylidene)(2)](+) (AuTMX(2)) was previously shown to selectively and potently stabilise telomeric DNA G‐quadruplex (G4) structures. This study sheds light on the molecular reactivity and mode of action of AuTMX(2) in the cellular context using mass spectrometry‐based methods, including shotgun proteomics in A2780 ovarian cancer cells. In contrast to other metal‐based anticancer agents, this organogold compound is less prone to form coordinative bonds with biological nucleophiles and is expected to exert its drug effects mainly by non‐covalent interactions. Global protein expression changes of treated cancer cells revealed a multimodal mode of action of AuTMX(2) by alterations in the nucleolus, telomeres, actin stress‐fibres and stress‐responses, which were further supported by pharmacological assays, fluorescence microscopy and cellular accumulation experiments. Proteomic data are available via ProteomeXchange with identifier PXD020560. John Wiley and Sons Inc. 2020-11-03 2020-12-01 /pmc/articles/PMC7756355/ /pubmed/32902006 http://dx.doi.org/10.1002/chem.202003495 Text en © 2020 The Authors. Published by Wiley-VCH GmbH This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Full Papers Meier‐Menches, Samuel M. Neuditschko, Benjamin Zappe, Katja Schaier, Martin Gerner, Marlene C. Schmetterer, Klaus G. Del Favero, Giorgia Bonsignore, Riccardo Cichna‐Markl, Margit Koellensperger, Gunda Casini, Angela Gerner, Christopher An Organometallic Gold(I) Bis‐N‐Heterocyclic Carbene Complex with Multimodal Activity in Ovarian Cancer Cells |
title | An Organometallic Gold(I) Bis‐N‐Heterocyclic Carbene Complex with Multimodal Activity in Ovarian Cancer Cells |
title_full | An Organometallic Gold(I) Bis‐N‐Heterocyclic Carbene Complex with Multimodal Activity in Ovarian Cancer Cells |
title_fullStr | An Organometallic Gold(I) Bis‐N‐Heterocyclic Carbene Complex with Multimodal Activity in Ovarian Cancer Cells |
title_full_unstemmed | An Organometallic Gold(I) Bis‐N‐Heterocyclic Carbene Complex with Multimodal Activity in Ovarian Cancer Cells |
title_short | An Organometallic Gold(I) Bis‐N‐Heterocyclic Carbene Complex with Multimodal Activity in Ovarian Cancer Cells |
title_sort | organometallic gold(i) bis‐n‐heterocyclic carbene complex with multimodal activity in ovarian cancer cells |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756355/ https://www.ncbi.nlm.nih.gov/pubmed/32902006 http://dx.doi.org/10.1002/chem.202003495 |
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