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An anti-glioblastoma gold(i)–NHC complex distorts mitochondrial morphology and bioenergetics to induce tumor growth inhibition

Glioblastoma multiforme (GBM) is the most lethal brain cancer subtype, often advanced by the time of initial diagnosis. Existing treatment modalities including surgery, chemotherapy and radiation have been stymied by recurrence, metastasis, drug resistance and brain targetability. Here, we report a...

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Detalles Bibliográficos
Autores principales: Greif, Charles E., Mertens, R. Tyler, Berger, Gilles, Parkin, Sean, Awuah, Samuel G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: RSC 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10398352/
https://www.ncbi.nlm.nih.gov/pubmed/37547458
http://dx.doi.org/10.1039/d3cb00051f
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author Greif, Charles E.
Mertens, R. Tyler
Berger, Gilles
Parkin, Sean
Awuah, Samuel G.
author_facet Greif, Charles E.
Mertens, R. Tyler
Berger, Gilles
Parkin, Sean
Awuah, Samuel G.
author_sort Greif, Charles E.
collection PubMed
description Glioblastoma multiforme (GBM) is the most lethal brain cancer subtype, often advanced by the time of initial diagnosis. Existing treatment modalities including surgery, chemotherapy and radiation have been stymied by recurrence, metastasis, drug resistance and brain targetability. Here, we report a geometrically distinct Au(i) complex ligated by N^N-bidentate ligands and supported by a N-heterocyclic ligand that modulates mitochondrial morphology to inhibit GBM in vitro and in vivo. This work benefits from the facile preparation of anti-GBM Au(i)-NHC complexes.
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spelling pubmed-103983522023-08-04 An anti-glioblastoma gold(i)–NHC complex distorts mitochondrial morphology and bioenergetics to induce tumor growth inhibition Greif, Charles E. Mertens, R. Tyler Berger, Gilles Parkin, Sean Awuah, Samuel G. RSC Chem Biol Chemistry Glioblastoma multiforme (GBM) is the most lethal brain cancer subtype, often advanced by the time of initial diagnosis. Existing treatment modalities including surgery, chemotherapy and radiation have been stymied by recurrence, metastasis, drug resistance and brain targetability. Here, we report a geometrically distinct Au(i) complex ligated by N^N-bidentate ligands and supported by a N-heterocyclic ligand that modulates mitochondrial morphology to inhibit GBM in vitro and in vivo. This work benefits from the facile preparation of anti-GBM Au(i)-NHC complexes. RSC 2023-05-25 /pmc/articles/PMC10398352/ /pubmed/37547458 http://dx.doi.org/10.1039/d3cb00051f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Greif, Charles E.
Mertens, R. Tyler
Berger, Gilles
Parkin, Sean
Awuah, Samuel G.
An anti-glioblastoma gold(i)–NHC complex distorts mitochondrial morphology and bioenergetics to induce tumor growth inhibition
title An anti-glioblastoma gold(i)–NHC complex distorts mitochondrial morphology and bioenergetics to induce tumor growth inhibition
title_full An anti-glioblastoma gold(i)–NHC complex distorts mitochondrial morphology and bioenergetics to induce tumor growth inhibition
title_fullStr An anti-glioblastoma gold(i)–NHC complex distorts mitochondrial morphology and bioenergetics to induce tumor growth inhibition
title_full_unstemmed An anti-glioblastoma gold(i)–NHC complex distorts mitochondrial morphology and bioenergetics to induce tumor growth inhibition
title_short An anti-glioblastoma gold(i)–NHC complex distorts mitochondrial morphology and bioenergetics to induce tumor growth inhibition
title_sort anti-glioblastoma gold(i)–nhc complex distorts mitochondrial morphology and bioenergetics to induce tumor growth inhibition
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10398352/
https://www.ncbi.nlm.nih.gov/pubmed/37547458
http://dx.doi.org/10.1039/d3cb00051f
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