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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...

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Autores principales: 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
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
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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.
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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
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