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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2023
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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. |
format | Online Article Text |
id | pubmed-10155491 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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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