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Mangrove derived Streptomyces sp. MUM265 as a potential source of antioxidant and anticolon-cancer agents

BACKGROUND: Colon cancer is the third most commonly diagnosed cancer worldwide, with a commensurately high mortality rate. The search for novel antioxidants and specific anticancer agents which may inhibit, delay or reverse the development of colon cancer is thus an area of great interest; Streptomy...

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Autores principales: Tan, Loh Teng-Hern, Chan, Kok-Gan, Pusparajah, Priyia, Yin, Wai-Fong, Khan, Tahir Mehmood, Lee, Learn-Han, Goh, Bey-Hing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6375222/
https://www.ncbi.nlm.nih.gov/pubmed/30760201
http://dx.doi.org/10.1186/s12866-019-1409-7
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author Tan, Loh Teng-Hern
Chan, Kok-Gan
Pusparajah, Priyia
Yin, Wai-Fong
Khan, Tahir Mehmood
Lee, Learn-Han
Goh, Bey-Hing
author_facet Tan, Loh Teng-Hern
Chan, Kok-Gan
Pusparajah, Priyia
Yin, Wai-Fong
Khan, Tahir Mehmood
Lee, Learn-Han
Goh, Bey-Hing
author_sort Tan, Loh Teng-Hern
collection PubMed
description BACKGROUND: Colon cancer is the third most commonly diagnosed cancer worldwide, with a commensurately high mortality rate. The search for novel antioxidants and specific anticancer agents which may inhibit, delay or reverse the development of colon cancer is thus an area of great interest; Streptomyces bacteria have been demonstrated to be a source of such agents. RESULTS: The extract from Streptomyces sp. MUM265— a strain which was isolated and identified from Kuala Selangor mangrove forest, Selangor, Malaysia— was analyzed and found to exhibit antioxidant properties as demonstrated via metal-chelating ability as well as superoxide anion, DPPH and ABTS radical scavenging activities. This study also showed that MUM265 extract demonstrated cytotoxicity against colon cancer cells as evidenced by the reduced cell viability of Caco-2 cell line. Treatment with MUM265 extract induced depolarization of mitochondrial membrane potential and accumulation of subG(1) cells in cell cycle analysis, suggesting that MUM265 exerted apoptosis-inducing effects on Caco-2 cells. CONCLUSION: These findings indicate that mangrove derived Streptomyces sp. MUM265 represents a valuable bioresource of bioactive compounds for the future development of chemopreventive agents, with particular promise suggested for treatment of colon cancer. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12866-019-1409-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-63752222019-02-26 Mangrove derived Streptomyces sp. MUM265 as a potential source of antioxidant and anticolon-cancer agents Tan, Loh Teng-Hern Chan, Kok-Gan Pusparajah, Priyia Yin, Wai-Fong Khan, Tahir Mehmood Lee, Learn-Han Goh, Bey-Hing BMC Microbiol Research Article BACKGROUND: Colon cancer is the third most commonly diagnosed cancer worldwide, with a commensurately high mortality rate. The search for novel antioxidants and specific anticancer agents which may inhibit, delay or reverse the development of colon cancer is thus an area of great interest; Streptomyces bacteria have been demonstrated to be a source of such agents. RESULTS: The extract from Streptomyces sp. MUM265— a strain which was isolated and identified from Kuala Selangor mangrove forest, Selangor, Malaysia— was analyzed and found to exhibit antioxidant properties as demonstrated via metal-chelating ability as well as superoxide anion, DPPH and ABTS radical scavenging activities. This study also showed that MUM265 extract demonstrated cytotoxicity against colon cancer cells as evidenced by the reduced cell viability of Caco-2 cell line. Treatment with MUM265 extract induced depolarization of mitochondrial membrane potential and accumulation of subG(1) cells in cell cycle analysis, suggesting that MUM265 exerted apoptosis-inducing effects on Caco-2 cells. CONCLUSION: These findings indicate that mangrove derived Streptomyces sp. MUM265 represents a valuable bioresource of bioactive compounds for the future development of chemopreventive agents, with particular promise suggested for treatment of colon cancer. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12866-019-1409-7) contains supplementary material, which is available to authorized users. BioMed Central 2019-02-13 /pmc/articles/PMC6375222/ /pubmed/30760201 http://dx.doi.org/10.1186/s12866-019-1409-7 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Tan, Loh Teng-Hern
Chan, Kok-Gan
Pusparajah, Priyia
Yin, Wai-Fong
Khan, Tahir Mehmood
Lee, Learn-Han
Goh, Bey-Hing
Mangrove derived Streptomyces sp. MUM265 as a potential source of antioxidant and anticolon-cancer agents
title Mangrove derived Streptomyces sp. MUM265 as a potential source of antioxidant and anticolon-cancer agents
title_full Mangrove derived Streptomyces sp. MUM265 as a potential source of antioxidant and anticolon-cancer agents
title_fullStr Mangrove derived Streptomyces sp. MUM265 as a potential source of antioxidant and anticolon-cancer agents
title_full_unstemmed Mangrove derived Streptomyces sp. MUM265 as a potential source of antioxidant and anticolon-cancer agents
title_short Mangrove derived Streptomyces sp. MUM265 as a potential source of antioxidant and anticolon-cancer agents
title_sort mangrove derived streptomyces sp. mum265 as a potential source of antioxidant and anticolon-cancer agents
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6375222/
https://www.ncbi.nlm.nih.gov/pubmed/30760201
http://dx.doi.org/10.1186/s12866-019-1409-7
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