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Anti-Cancer and Anti-Inflammatory Activities of Three New Chromone Derivatives from the Marine-Derived Penicillium citrinum

Three new and uncommon chromone analogs, epiremisporine F (1), epiremisporine G (2), and epiremisporine H (3), were isolated from marine-origin Penicillium citrinum. Among the isolated compounds, compounds 2–3 remarkably suppressed fMLP-induced superoxide anion generation by human neutrophils, with...

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Autores principales: Chu, Yi-Cheng, Chang, Chun-Hao, Liao, Hsiang-Ruei, Fu, Shu-Ling, Chen, Jih-Jung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8398383/
https://www.ncbi.nlm.nih.gov/pubmed/34436247
http://dx.doi.org/10.3390/md19080408
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author Chu, Yi-Cheng
Chang, Chun-Hao
Liao, Hsiang-Ruei
Fu, Shu-Ling
Chen, Jih-Jung
author_facet Chu, Yi-Cheng
Chang, Chun-Hao
Liao, Hsiang-Ruei
Fu, Shu-Ling
Chen, Jih-Jung
author_sort Chu, Yi-Cheng
collection PubMed
description Three new and uncommon chromone analogs, epiremisporine F (1), epiremisporine G (2), and epiremisporine H (3), were isolated from marine-origin Penicillium citrinum. Among the isolated compounds, compounds 2–3 remarkably suppressed fMLP-induced superoxide anion generation by human neutrophils, with IC(50) values of 31.68 ± 2.53, and 33.52 ± 0.42 μM, respectively. Compound 3 exhibited cytotoxic activities against human colon carcinoma (HT-29) and non-small lung cancer cell (A549) with IC(50) values of 21.17 ± 4.89 and 31.43 ± 3.01 μM, respectively, and Western blot assay confirmed that compound 3 obviously induced apoptosis of HT-29 cells, via Bcl-2, Bax, and caspase 3 signaling cascades.
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spelling pubmed-83983832021-08-29 Anti-Cancer and Anti-Inflammatory Activities of Three New Chromone Derivatives from the Marine-Derived Penicillium citrinum Chu, Yi-Cheng Chang, Chun-Hao Liao, Hsiang-Ruei Fu, Shu-Ling Chen, Jih-Jung Mar Drugs Article Three new and uncommon chromone analogs, epiremisporine F (1), epiremisporine G (2), and epiremisporine H (3), were isolated from marine-origin Penicillium citrinum. Among the isolated compounds, compounds 2–3 remarkably suppressed fMLP-induced superoxide anion generation by human neutrophils, with IC(50) values of 31.68 ± 2.53, and 33.52 ± 0.42 μM, respectively. Compound 3 exhibited cytotoxic activities against human colon carcinoma (HT-29) and non-small lung cancer cell (A549) with IC(50) values of 21.17 ± 4.89 and 31.43 ± 3.01 μM, respectively, and Western blot assay confirmed that compound 3 obviously induced apoptosis of HT-29 cells, via Bcl-2, Bax, and caspase 3 signaling cascades. MDPI 2021-07-23 /pmc/articles/PMC8398383/ /pubmed/34436247 http://dx.doi.org/10.3390/md19080408 Text en © 2021 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
Chu, Yi-Cheng
Chang, Chun-Hao
Liao, Hsiang-Ruei
Fu, Shu-Ling
Chen, Jih-Jung
Anti-Cancer and Anti-Inflammatory Activities of Three New Chromone Derivatives from the Marine-Derived Penicillium citrinum
title Anti-Cancer and Anti-Inflammatory Activities of Three New Chromone Derivatives from the Marine-Derived Penicillium citrinum
title_full Anti-Cancer and Anti-Inflammatory Activities of Three New Chromone Derivatives from the Marine-Derived Penicillium citrinum
title_fullStr Anti-Cancer and Anti-Inflammatory Activities of Three New Chromone Derivatives from the Marine-Derived Penicillium citrinum
title_full_unstemmed Anti-Cancer and Anti-Inflammatory Activities of Three New Chromone Derivatives from the Marine-Derived Penicillium citrinum
title_short Anti-Cancer and Anti-Inflammatory Activities of Three New Chromone Derivatives from the Marine-Derived Penicillium citrinum
title_sort anti-cancer and anti-inflammatory activities of three new chromone derivatives from the marine-derived penicillium citrinum
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8398383/
https://www.ncbi.nlm.nih.gov/pubmed/34436247
http://dx.doi.org/10.3390/md19080408
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