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Zampanolide and dactylolide: cytotoxic tubulin-assembly agents and promising anticancer leads

Covering: through January 2014 Zampanolide is a marine natural macrolide and a recent addition to the family of microtubule-stabilizing cytotoxic agents. Zampanolide exhibits unique effects on tubulin assembly and is more potent than paclitaxel against several multi-drug resistant cancer cell lines....

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Detalles Bibliográficos
Autores principales: Chen, Qiao-Hong, Kingston, David G. I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4126874/
https://www.ncbi.nlm.nih.gov/pubmed/24945566
http://dx.doi.org/10.1039/c4np00024b
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author Chen, Qiao-Hong
Kingston, David G. I.
author_facet Chen, Qiao-Hong
Kingston, David G. I.
author_sort Chen, Qiao-Hong
collection PubMed
description Covering: through January 2014 Zampanolide is a marine natural macrolide and a recent addition to the family of microtubule-stabilizing cytotoxic agents. Zampanolide exhibits unique effects on tubulin assembly and is more potent than paclitaxel against several multi-drug resistant cancer cell lines. A high-resolution crystal structure of αβ-tubulin in complex with zampanolide explains how taxane-site microtubule-stabilizing agents promote microtubule assemble and stability. This review provides an overview of current developments of zampanolide and its related but less potent analogue dactylolide, covering their natural sources and isolation, structure and conformation, cytotoxic potential, structure–activity studies, mechanism of action, and syntheses.
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spelling pubmed-41268742015-02-23 Zampanolide and dactylolide: cytotoxic tubulin-assembly agents and promising anticancer leads Chen, Qiao-Hong Kingston, David G. I. Nat Prod Rep Chemistry Covering: through January 2014 Zampanolide is a marine natural macrolide and a recent addition to the family of microtubule-stabilizing cytotoxic agents. Zampanolide exhibits unique effects on tubulin assembly and is more potent than paclitaxel against several multi-drug resistant cancer cell lines. A high-resolution crystal structure of αβ-tubulin in complex with zampanolide explains how taxane-site microtubule-stabilizing agents promote microtubule assemble and stability. This review provides an overview of current developments of zampanolide and its related but less potent analogue dactylolide, covering their natural sources and isolation, structure and conformation, cytotoxic potential, structure–activity studies, mechanism of action, and syntheses. Royal Society of Chemistry 2014-09-06 2014-06-19 /pmc/articles/PMC4126874/ /pubmed/24945566 http://dx.doi.org/10.1039/c4np00024b Text en This journal is © The Royal Society of Chemistry 2014 http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 Unported License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Chemistry
Chen, Qiao-Hong
Kingston, David G. I.
Zampanolide and dactylolide: cytotoxic tubulin-assembly agents and promising anticancer leads
title Zampanolide and dactylolide: cytotoxic tubulin-assembly agents and promising anticancer leads
title_full Zampanolide and dactylolide: cytotoxic tubulin-assembly agents and promising anticancer leads
title_fullStr Zampanolide and dactylolide: cytotoxic tubulin-assembly agents and promising anticancer leads
title_full_unstemmed Zampanolide and dactylolide: cytotoxic tubulin-assembly agents and promising anticancer leads
title_short Zampanolide and dactylolide: cytotoxic tubulin-assembly agents and promising anticancer leads
title_sort zampanolide and dactylolide: cytotoxic tubulin-assembly agents and promising anticancer leads
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4126874/
https://www.ncbi.nlm.nih.gov/pubmed/24945566
http://dx.doi.org/10.1039/c4np00024b
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