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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...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
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
Descripción
Sumario: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.