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Oxazolomycins produced by Streptomyces glaucus and their cytotoxic activity
Six oxazolomycins (1–6) were isolated from the fermentation broth of a soil-borne bacterial strain, Streptomyces glaucus. The structures of the new compounds, oxazolomycins D–F (1–3) and glaucumycins A, B (6a/6b), were elucidated by detailed spectroscopic data analysis. Oxazolomycins 1, 2, 4, and 5...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9042891/ https://www.ncbi.nlm.nih.gov/pubmed/35494745 http://dx.doi.org/10.1039/d1ra06182h |
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author | Mu, Yu Jiang, Yi Qu, Xiaodan Liu, Bo Tan, Junfeng Li, Guiding Jiang, Mingguo Li, Liya Han, Li Huang, Xueshi |
author_facet | Mu, Yu Jiang, Yi Qu, Xiaodan Liu, Bo Tan, Junfeng Li, Guiding Jiang, Mingguo Li, Liya Han, Li Huang, Xueshi |
author_sort | Mu, Yu |
collection | PubMed |
description | Six oxazolomycins (1–6) were isolated from the fermentation broth of a soil-borne bacterial strain, Streptomyces glaucus. The structures of the new compounds, oxazolomycins D–F (1–3) and glaucumycins A, B (6a/6b), were elucidated by detailed spectroscopic data analysis. Oxazolomycins 1, 2, 4, and 5 demonstrated weak or modest cytotoxic activities against four human cancer cell lines, with IC(50) values ranging from 10.6 ± 1.7 to 89.5 ± 6.6 μM (or >100 μM). Further study showed that 4 caused S phase cell cycle arrest in SMMC7721 cells through down-regulating the protein expression of cyclin A2, CDK2. Meanwhile, 4 induced apoptosis in SMMC7721 cells through down-regulating the protein levels of Bcl-2, up-regulating the levels of Bax, and activating the cleavage of caspase-3. |
format | Online Article Text |
id | pubmed-9042891 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90428912022-04-28 Oxazolomycins produced by Streptomyces glaucus and their cytotoxic activity Mu, Yu Jiang, Yi Qu, Xiaodan Liu, Bo Tan, Junfeng Li, Guiding Jiang, Mingguo Li, Liya Han, Li Huang, Xueshi RSC Adv Chemistry Six oxazolomycins (1–6) were isolated from the fermentation broth of a soil-borne bacterial strain, Streptomyces glaucus. The structures of the new compounds, oxazolomycins D–F (1–3) and glaucumycins A, B (6a/6b), were elucidated by detailed spectroscopic data analysis. Oxazolomycins 1, 2, 4, and 5 demonstrated weak or modest cytotoxic activities against four human cancer cell lines, with IC(50) values ranging from 10.6 ± 1.7 to 89.5 ± 6.6 μM (or >100 μM). Further study showed that 4 caused S phase cell cycle arrest in SMMC7721 cells through down-regulating the protein expression of cyclin A2, CDK2. Meanwhile, 4 induced apoptosis in SMMC7721 cells through down-regulating the protein levels of Bcl-2, up-regulating the levels of Bax, and activating the cleavage of caspase-3. The Royal Society of Chemistry 2021-10-28 /pmc/articles/PMC9042891/ /pubmed/35494745 http://dx.doi.org/10.1039/d1ra06182h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Mu, Yu Jiang, Yi Qu, Xiaodan Liu, Bo Tan, Junfeng Li, Guiding Jiang, Mingguo Li, Liya Han, Li Huang, Xueshi Oxazolomycins produced by Streptomyces glaucus and their cytotoxic activity |
title | Oxazolomycins produced by Streptomyces glaucus and their cytotoxic activity |
title_full | Oxazolomycins produced by Streptomyces glaucus and their cytotoxic activity |
title_fullStr | Oxazolomycins produced by Streptomyces glaucus and their cytotoxic activity |
title_full_unstemmed | Oxazolomycins produced by Streptomyces glaucus and their cytotoxic activity |
title_short | Oxazolomycins produced by Streptomyces glaucus and their cytotoxic activity |
title_sort | oxazolomycins produced by streptomyces glaucus and their cytotoxic activity |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9042891/ https://www.ncbi.nlm.nih.gov/pubmed/35494745 http://dx.doi.org/10.1039/d1ra06182h |
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