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LZY3016, a novel geldanamycin derivative, inhibits tumor growth in an MDA-MB-231 xenograft model

A novel geldanamycin derivative LZY3016 was synthesized as an antitumor agent. Compound LZY3016 exhibited potent anti-proliferation activity toward MDA-MB-231 (IC(50) = 0.06 μM), which was more effective than positive drug 17-AAG. In vivo hepatotoxicity assay displayed that serum AST/ALT levels in L...

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Detalles Bibliográficos
Autores principales: Li, Zhenyu, Jia, Lejiao, Tang, Hui, Shen, Yuemao, Shen, Chengwu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10155491/
https://www.ncbi.nlm.nih.gov/pubmed/37152572
http://dx.doi.org/10.1039/d3ra02131a
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author Li, Zhenyu
Jia, Lejiao
Tang, Hui
Shen, Yuemao
Shen, Chengwu
author_facet Li, Zhenyu
Jia, Lejiao
Tang, Hui
Shen, Yuemao
Shen, Chengwu
author_sort Li, Zhenyu
collection PubMed
description A novel geldanamycin derivative LZY3016 was synthesized as an antitumor agent. Compound LZY3016 exhibited potent anti-proliferation activity toward MDA-MB-231 (IC(50) = 0.06 μM), which was more effective than positive drug 17-AAG. In vivo hepatotoxicity assay displayed that serum AST/ALT levels in LZY3016-treated mice were both significantly less than those in the geldanamycin (GA) group. LZY3016 showed potent antitumor activity in an MDA-MB-231 xenograft mouse model, suggesting LZY3016 is an up-and-coming antitumor candidate. The theoretical binding mode between LZY3016 and Hsp90 was obtained by molecular dynamics simulation.
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spelling pubmed-101554912023-05-04 LZY3016, a novel geldanamycin derivative, inhibits tumor growth in an MDA-MB-231 xenograft model Li, Zhenyu Jia, Lejiao Tang, Hui Shen, Yuemao Shen, Chengwu RSC Adv Chemistry A novel geldanamycin derivative LZY3016 was synthesized as an antitumor agent. Compound LZY3016 exhibited potent anti-proliferation activity toward MDA-MB-231 (IC(50) = 0.06 μM), which was more effective than positive drug 17-AAG. In vivo hepatotoxicity assay displayed that serum AST/ALT levels in LZY3016-treated mice were both significantly less than those in the geldanamycin (GA) group. LZY3016 showed potent antitumor activity in an MDA-MB-231 xenograft mouse model, suggesting LZY3016 is an up-and-coming antitumor candidate. The theoretical binding mode between LZY3016 and Hsp90 was obtained by molecular dynamics simulation. The Royal Society of Chemistry 2023-05-03 /pmc/articles/PMC10155491/ /pubmed/37152572 http://dx.doi.org/10.1039/d3ra02131a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Li, Zhenyu
Jia, Lejiao
Tang, Hui
Shen, Yuemao
Shen, Chengwu
LZY3016, a novel geldanamycin derivative, inhibits tumor growth in an MDA-MB-231 xenograft model
title LZY3016, a novel geldanamycin derivative, inhibits tumor growth in an MDA-MB-231 xenograft model
title_full LZY3016, a novel geldanamycin derivative, inhibits tumor growth in an MDA-MB-231 xenograft model
title_fullStr LZY3016, a novel geldanamycin derivative, inhibits tumor growth in an MDA-MB-231 xenograft model
title_full_unstemmed LZY3016, a novel geldanamycin derivative, inhibits tumor growth in an MDA-MB-231 xenograft model
title_short LZY3016, a novel geldanamycin derivative, inhibits tumor growth in an MDA-MB-231 xenograft model
title_sort lzy3016, a novel geldanamycin derivative, inhibits tumor growth in an mda-mb-231 xenograft model
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10155491/
https://www.ncbi.nlm.nih.gov/pubmed/37152572
http://dx.doi.org/10.1039/d3ra02131a
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