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Gold(III)-P-chirogenic complex induces mitochondrial dysfunction in triple-negative breast cancer
Chemical agents that specifically exploit metabolic vulnerabilities of cancer cells will be beneficial but are rare. The role of oxidative phosphorylation (OXPHOS) in promoting and maintaining triple-negative breast cancer (TNBC) growth provides new treatment opportunity. In this work, we describe A...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9117869/ https://www.ncbi.nlm.nih.gov/pubmed/35602949 http://dx.doi.org/10.1016/j.isci.2022.104340 |
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author | Olelewe, Chibuzor Kim, Jong Hyun Ofori, Samuel Mertens, Randall T. Gukathasan, Sailajah Awuah, Samuel G. |
author_facet | Olelewe, Chibuzor Kim, Jong Hyun Ofori, Samuel Mertens, Randall T. Gukathasan, Sailajah Awuah, Samuel G. |
author_sort | Olelewe, Chibuzor |
collection | PubMed |
description | Chemical agents that specifically exploit metabolic vulnerabilities of cancer cells will be beneficial but are rare. The role of oxidative phosphorylation (OXPHOS) in promoting and maintaining triple-negative breast cancer (TNBC) growth provides new treatment opportunity. In this work, we describe AuPhos-19, a small-molecule gold(III)-based agent bearing a chiral phosphine ligand that selectively disrupts mitochondrial metabolism in murine and human TNBC cells but not normal epithelial cells. AuPhos-19 induces potent cytotoxic effect with half maximal inhibitory concentration (IC(50)) in the nanomolar range (220–650 nM) across different TNBC cell lines. The lipophilic cationic character of AuPhos-19 facilitates interaction with mitochondrial OXPHOS. AuPhos-19 inhibits mitochondria respiration and induces significant AMPK activation. Depolarization of the mitochondria membrane, mitochondria ROS accumulation, and mitochondria DNA depletion provided further indication that AuPhos-19 perturbs mitochondria function. AuPhos-19 inhibits tumor growth in tumor-bearing mice. This study highlights the development of gold-based compounds targeting mitochondrial pathways for efficacious cancer treatment. |
format | Online Article Text |
id | pubmed-9117869 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-91178692022-05-20 Gold(III)-P-chirogenic complex induces mitochondrial dysfunction in triple-negative breast cancer Olelewe, Chibuzor Kim, Jong Hyun Ofori, Samuel Mertens, Randall T. Gukathasan, Sailajah Awuah, Samuel G. iScience Article Chemical agents that specifically exploit metabolic vulnerabilities of cancer cells will be beneficial but are rare. The role of oxidative phosphorylation (OXPHOS) in promoting and maintaining triple-negative breast cancer (TNBC) growth provides new treatment opportunity. In this work, we describe AuPhos-19, a small-molecule gold(III)-based agent bearing a chiral phosphine ligand that selectively disrupts mitochondrial metabolism in murine and human TNBC cells but not normal epithelial cells. AuPhos-19 induces potent cytotoxic effect with half maximal inhibitory concentration (IC(50)) in the nanomolar range (220–650 nM) across different TNBC cell lines. The lipophilic cationic character of AuPhos-19 facilitates interaction with mitochondrial OXPHOS. AuPhos-19 inhibits mitochondria respiration and induces significant AMPK activation. Depolarization of the mitochondria membrane, mitochondria ROS accumulation, and mitochondria DNA depletion provided further indication that AuPhos-19 perturbs mitochondria function. AuPhos-19 inhibits tumor growth in tumor-bearing mice. This study highlights the development of gold-based compounds targeting mitochondrial pathways for efficacious cancer treatment. Elsevier 2022-04-30 /pmc/articles/PMC9117869/ /pubmed/35602949 http://dx.doi.org/10.1016/j.isci.2022.104340 Text en © 2022. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Olelewe, Chibuzor Kim, Jong Hyun Ofori, Samuel Mertens, Randall T. Gukathasan, Sailajah Awuah, Samuel G. Gold(III)-P-chirogenic complex induces mitochondrial dysfunction in triple-negative breast cancer |
title | Gold(III)-P-chirogenic complex induces mitochondrial dysfunction in triple-negative breast cancer |
title_full | Gold(III)-P-chirogenic complex induces mitochondrial dysfunction in triple-negative breast cancer |
title_fullStr | Gold(III)-P-chirogenic complex induces mitochondrial dysfunction in triple-negative breast cancer |
title_full_unstemmed | Gold(III)-P-chirogenic complex induces mitochondrial dysfunction in triple-negative breast cancer |
title_short | Gold(III)-P-chirogenic complex induces mitochondrial dysfunction in triple-negative breast cancer |
title_sort | gold(iii)-p-chirogenic complex induces mitochondrial dysfunction in triple-negative breast cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9117869/ https://www.ncbi.nlm.nih.gov/pubmed/35602949 http://dx.doi.org/10.1016/j.isci.2022.104340 |
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