Epothilones as Natural Compounds for Novel Anticancer Drugs Development
Primer Autor |
Paz, Cristian
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Co-autores |
Villegas, Cecilia
Gonzalez-Chavarria, Ivan
Burgos, Viviana
Iturra-Beiza, Hector
Ulrich, Henning
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Título |
Epothilones as Natural Compounds for Novel Anticancer Drugs Development
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Editorial |
MDPI
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Revista |
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
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Lenguaje |
en
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Resumen |
Epothilone is a natural 16-membered macrolide cytotoxic compound produced by the metabolism of the cellulose-degrading myxobacterium Sorangium cellulosum. This review summarizes results in the study of epothilones against cancer with preclinical results and clinical studies from 2010-2022. Epothilone have mechanisms of action similar to paclitaxel by inducing tubulin polymerization and apoptosis with low susceptibility to tumor resistance mechanisms. It is active against refractory tumors, being superior to paclitaxel in many respects. Since the discovery of epothilones, several derivatives have been synthesized, and most of them have failed in Phases II and III in clinical trials, however, ixabepilone and utidelone are currently used in clinical practice. There is robust evidence that triple-negative breast cancer (TNBC) treatment improves using ixabepilone plus capecitabine or utidelone in combination with capecitabine. In recent years innovative synthetic strategies resulted in the synthesis of new epothilone derivatives with improved activity against refractory tumors with better activities when compared to ixabepilone or taxol. These compounds together with specific delivery mechanisms could be developed in anti-cancer drugs.
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Fecha Publicación |
2023
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Tipo de Recurso |
artículo de revisión
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doi |
10.3390/ijms24076063
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Formato Recurso |
PDF
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Palabras Claves |
epothilones
epothilone derivates
cytotoxicity
anticancer agents
refractory cancer
taxanes
clinical trials
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Ubicación del archivo | |
Categoría OCDE |
Bioquímica y biología molecular
Química
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Materias |
epotilonas
derivados de epotilona
citotoxicidad
agentes anticancerígenos
cáncer refractario
taxanos
ensayos clínicos
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Identificador del recurso (Mandatado-único) |
artículo de revisión
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Versión del recurso (Recomendado-único) |
versión publicada
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License |
CC BY 4.0
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Condición de la licencia (Recomendado-repetible) |
CC BY 4.0
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Derechos de acceso |
acceso abierto
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Access Rights |
acceso abierto
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Id de Web of Science |
WOS:000969832300001
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ISSN |
1661-6596
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Tipo de ruta |
verde# dorado
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Categoría WOS |
Bioquímica y biología molecular
Química
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Referencia del Financiador (Mandatado si es aplicable-repetible) |
FAPESP 2018/07366-4
FAPESP 201808426-0
ANID-FONDECYT 1220831
ANID FONDECYT 11181105
ANID FONDECYT 1220831
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