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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
RSC
2023
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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. |
format | Online Article Text |
id | pubmed-10398352 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | RSC |
record_format | MEDLINE/PubMed |
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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