Cargando…
Probing Anti-Leukemic Metabolites from Marine-Derived Streptomyces sp. LY1209
The unmet need for specific anti-leukemic agents for the treatment of acute lymphoblastic leukemia led us to screen a variety of marine-derived bacteria. The fermentation broth extract of Streptomyces sp. LY1209 exhibited the most potent anti-proliferative effect against Molt 4 leukemia cells. A chr...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9025307/ https://www.ncbi.nlm.nih.gov/pubmed/35448507 http://dx.doi.org/10.3390/metabo12040320 |
_version_ | 1784690837686321152 |
---|---|
author | Chen, You-Ying Chen, Lo-Yun Chen, Po-Jen El-Shazly, Mohamed Peng, Bo-Rong Chen, Yu-Cheng Su, Chun-Han Su, Jui-Hsin Sung, Ping-Jyun Yen, Pei-Tzu Wang, Lung-Shuo Lai, Kuei-Hung |
author_facet | Chen, You-Ying Chen, Lo-Yun Chen, Po-Jen El-Shazly, Mohamed Peng, Bo-Rong Chen, Yu-Cheng Su, Chun-Han Su, Jui-Hsin Sung, Ping-Jyun Yen, Pei-Tzu Wang, Lung-Shuo Lai, Kuei-Hung |
author_sort | Chen, You-Ying |
collection | PubMed |
description | The unmet need for specific anti-leukemic agents for the treatment of acute lymphoblastic leukemia led us to screen a variety of marine-derived bacteria. The fermentation broth extract of Streptomyces sp. LY1209 exhibited the most potent anti-proliferative effect against Molt 4 leukemia cells. A chromatographic anti-proliferative profiling approach was applied to characterize the metabolites with bioactive potential. Among all the metabolites, the major anti-leukemic constituents were staurosporine and a series of diketopiperazines (DKPs), including one novel and two known DKPs identified from nature for the first time. The structures of these compounds were identified using extensive spectroscopic analysis. The anti-proliferative potential of these metabolites against the Molt 4 cancer cell line was also determined. According to the in silico analysis utilizing a chemical global positioning system for natural products (ChemGPS-NP), it was suggested that these DKPs are potential anti-microtubule and alkylating agents, while staurosporine was proposed to be a tyrosine kinase inhibitor. Our findings not only identified a series of anti-proliferative metabolites, but also suggested a strategic workflow for the future discovery of natural product drug leads. |
format | Online Article Text |
id | pubmed-9025307 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-90253072022-04-23 Probing Anti-Leukemic Metabolites from Marine-Derived Streptomyces sp. LY1209 Chen, You-Ying Chen, Lo-Yun Chen, Po-Jen El-Shazly, Mohamed Peng, Bo-Rong Chen, Yu-Cheng Su, Chun-Han Su, Jui-Hsin Sung, Ping-Jyun Yen, Pei-Tzu Wang, Lung-Shuo Lai, Kuei-Hung Metabolites Article The unmet need for specific anti-leukemic agents for the treatment of acute lymphoblastic leukemia led us to screen a variety of marine-derived bacteria. The fermentation broth extract of Streptomyces sp. LY1209 exhibited the most potent anti-proliferative effect against Molt 4 leukemia cells. A chromatographic anti-proliferative profiling approach was applied to characterize the metabolites with bioactive potential. Among all the metabolites, the major anti-leukemic constituents were staurosporine and a series of diketopiperazines (DKPs), including one novel and two known DKPs identified from nature for the first time. The structures of these compounds were identified using extensive spectroscopic analysis. The anti-proliferative potential of these metabolites against the Molt 4 cancer cell line was also determined. According to the in silico analysis utilizing a chemical global positioning system for natural products (ChemGPS-NP), it was suggested that these DKPs are potential anti-microtubule and alkylating agents, while staurosporine was proposed to be a tyrosine kinase inhibitor. Our findings not only identified a series of anti-proliferative metabolites, but also suggested a strategic workflow for the future discovery of natural product drug leads. MDPI 2022-04-02 /pmc/articles/PMC9025307/ /pubmed/35448507 http://dx.doi.org/10.3390/metabo12040320 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Chen, You-Ying Chen, Lo-Yun Chen, Po-Jen El-Shazly, Mohamed Peng, Bo-Rong Chen, Yu-Cheng Su, Chun-Han Su, Jui-Hsin Sung, Ping-Jyun Yen, Pei-Tzu Wang, Lung-Shuo Lai, Kuei-Hung Probing Anti-Leukemic Metabolites from Marine-Derived Streptomyces sp. LY1209 |
title | Probing Anti-Leukemic Metabolites from Marine-Derived Streptomyces sp. LY1209 |
title_full | Probing Anti-Leukemic Metabolites from Marine-Derived Streptomyces sp. LY1209 |
title_fullStr | Probing Anti-Leukemic Metabolites from Marine-Derived Streptomyces sp. LY1209 |
title_full_unstemmed | Probing Anti-Leukemic Metabolites from Marine-Derived Streptomyces sp. LY1209 |
title_short | Probing Anti-Leukemic Metabolites from Marine-Derived Streptomyces sp. LY1209 |
title_sort | probing anti-leukemic metabolites from marine-derived streptomyces sp. ly1209 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9025307/ https://www.ncbi.nlm.nih.gov/pubmed/35448507 http://dx.doi.org/10.3390/metabo12040320 |
work_keys_str_mv | AT chenyouying probingantileukemicmetabolitesfrommarinederivedstreptomycessply1209 AT chenloyun probingantileukemicmetabolitesfrommarinederivedstreptomycessply1209 AT chenpojen probingantileukemicmetabolitesfrommarinederivedstreptomycessply1209 AT elshazlymohamed probingantileukemicmetabolitesfrommarinederivedstreptomycessply1209 AT pengborong probingantileukemicmetabolitesfrommarinederivedstreptomycessply1209 AT chenyucheng probingantileukemicmetabolitesfrommarinederivedstreptomycessply1209 AT suchunhan probingantileukemicmetabolitesfrommarinederivedstreptomycessply1209 AT sujuihsin probingantileukemicmetabolitesfrommarinederivedstreptomycessply1209 AT sungpingjyun probingantileukemicmetabolitesfrommarinederivedstreptomycessply1209 AT yenpeitzu probingantileukemicmetabolitesfrommarinederivedstreptomycessply1209 AT wanglungshuo probingantileukemicmetabolitesfrommarinederivedstreptomycessply1209 AT laikueihung probingantileukemicmetabolitesfrommarinederivedstreptomycessply1209 |