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Inhibition of Topoisomerases by Metal Thiosemicarbazone Complexes
Topoisomerases, common targets for anti-cancer therapeutics, are crucial enzymes for DNA replication, transcription, and many other aspects of DNA metabolism. The potential anti-cancer effects of thiosemicarbazones (TSC) and metal–TSC complexes have been demonstrated to target several biological pro...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10419228/ https://www.ncbi.nlm.nih.gov/pubmed/37569386 http://dx.doi.org/10.3390/ijms241512010 |
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author | Jiang, Xiaohua Fielding, Lauren A. Davis, Hunter Carroll, William Lisic, Edward C. Deweese, Joseph E. |
author_facet | Jiang, Xiaohua Fielding, Lauren A. Davis, Hunter Carroll, William Lisic, Edward C. Deweese, Joseph E. |
author_sort | Jiang, Xiaohua |
collection | PubMed |
description | Topoisomerases, common targets for anti-cancer therapeutics, are crucial enzymes for DNA replication, transcription, and many other aspects of DNA metabolism. The potential anti-cancer effects of thiosemicarbazones (TSC) and metal–TSC complexes have been demonstrated to target several biological processes, including DNA metabolism. Human topoisomerases were discovered among the molecular targets for TSCs, and metal-chelated TSCs specifically displayed significant inhibition of topoisomerase II. The processes by which metal–TSCs or TSCs inhibit topoisomerases are still being studied. In this brief review, we summarize the TSCs and metal–TSCs that inhibit various types of human topoisomerases, and we note some of the key unanswered questions regarding this interesting class of diverse compounds. |
format | Online Article Text |
id | pubmed-10419228 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-104192282023-08-12 Inhibition of Topoisomerases by Metal Thiosemicarbazone Complexes Jiang, Xiaohua Fielding, Lauren A. Davis, Hunter Carroll, William Lisic, Edward C. Deweese, Joseph E. Int J Mol Sci Review Topoisomerases, common targets for anti-cancer therapeutics, are crucial enzymes for DNA replication, transcription, and many other aspects of DNA metabolism. The potential anti-cancer effects of thiosemicarbazones (TSC) and metal–TSC complexes have been demonstrated to target several biological processes, including DNA metabolism. Human topoisomerases were discovered among the molecular targets for TSCs, and metal-chelated TSCs specifically displayed significant inhibition of topoisomerase II. The processes by which metal–TSCs or TSCs inhibit topoisomerases are still being studied. In this brief review, we summarize the TSCs and metal–TSCs that inhibit various types of human topoisomerases, and we note some of the key unanswered questions regarding this interesting class of diverse compounds. MDPI 2023-07-27 /pmc/articles/PMC10419228/ /pubmed/37569386 http://dx.doi.org/10.3390/ijms241512010 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Jiang, Xiaohua Fielding, Lauren A. Davis, Hunter Carroll, William Lisic, Edward C. Deweese, Joseph E. Inhibition of Topoisomerases by Metal Thiosemicarbazone Complexes |
title | Inhibition of Topoisomerases by Metal Thiosemicarbazone Complexes |
title_full | Inhibition of Topoisomerases by Metal Thiosemicarbazone Complexes |
title_fullStr | Inhibition of Topoisomerases by Metal Thiosemicarbazone Complexes |
title_full_unstemmed | Inhibition of Topoisomerases by Metal Thiosemicarbazone Complexes |
title_short | Inhibition of Topoisomerases by Metal Thiosemicarbazone Complexes |
title_sort | inhibition of topoisomerases by metal thiosemicarbazone complexes |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10419228/ https://www.ncbi.nlm.nih.gov/pubmed/37569386 http://dx.doi.org/10.3390/ijms241512010 |
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