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Production of Terretonin N and Butyrolactone I by Thermophilic Aspergillus terreus TM8 Promoted Apoptosis and Cell Death in Human Prostate and Ovarian Cancer Cells

The anticancer activity of terretonin N (1) and butyrolactone I (2), obtained from the thermophilic fungus Aspergillus terreus TM8, was intensively studied against prostate adenocarcinoma (PC-3) and ovary adenocarcinoma (SKOV3) human cell lines. According to this study, both compounds showed potent...

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Autores principales: Ghfar, Ayman A., El-Metwally, Mohammad Magdy, Shaaban, Mohamed, Gabr, Sami A., Gabr, Nada S., Diab, Marwa S. M., Aqel, Ahmad, Habila, Mohamed A., Al-Qahtani, Wahidah H., Alfaifi, Mohammad Y., Elbehairi, Serag Eldin I., AlJumah, Bayan Ahmed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8126039/
https://www.ncbi.nlm.nih.gov/pubmed/34068647
http://dx.doi.org/10.3390/molecules26092816
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author Ghfar, Ayman A.
El-Metwally, Mohammad Magdy
Shaaban, Mohamed
Gabr, Sami A.
Gabr, Nada S.
Diab, Marwa S. M.
Aqel, Ahmad
Habila, Mohamed A.
Al-Qahtani, Wahidah H.
Alfaifi, Mohammad Y.
Elbehairi, Serag Eldin I.
AlJumah, Bayan Ahmed
author_facet Ghfar, Ayman A.
El-Metwally, Mohammad Magdy
Shaaban, Mohamed
Gabr, Sami A.
Gabr, Nada S.
Diab, Marwa S. M.
Aqel, Ahmad
Habila, Mohamed A.
Al-Qahtani, Wahidah H.
Alfaifi, Mohammad Y.
Elbehairi, Serag Eldin I.
AlJumah, Bayan Ahmed
author_sort Ghfar, Ayman A.
collection PubMed
description The anticancer activity of terretonin N (1) and butyrolactone I (2), obtained from the thermophilic fungus Aspergillus terreus TM8, was intensively studied against prostate adenocarcinoma (PC-3) and ovary adenocarcinoma (SKOV3) human cell lines. According to this study, both compounds showed potent cytotoxicity towards ovarian adenocarcinoma cells (SKOV3) with IC(50) 1.2 and 0.6 μg/mL, respectively. With respect to metastatic prostate cells (PC-3), the two compounds 1 and 2 showed a significantly promising cytotoxicity effect with IC(50) of 7.4 and 4.5 μg/mL, respectively. The tested fungal metabolites showed higher rates of early and late apoptosis with little or no necrotic apoptotic pathway in all treated prostate adenocarcinoma (PC-3) and ovary adenocarcinoma (SKOV3) human cell lines, respectively. The results reported in this study confirmed the promising biological properties of terretonin N (1) and butyrolactone I (2) as anticancer agents via the induction of cellular apoptosis. However, further studies are needed to elucidate the molecular mechanism by which cellular apoptosis is induced in cancer cells.
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spelling pubmed-81260392021-05-17 Production of Terretonin N and Butyrolactone I by Thermophilic Aspergillus terreus TM8 Promoted Apoptosis and Cell Death in Human Prostate and Ovarian Cancer Cells Ghfar, Ayman A. El-Metwally, Mohammad Magdy Shaaban, Mohamed Gabr, Sami A. Gabr, Nada S. Diab, Marwa S. M. Aqel, Ahmad Habila, Mohamed A. Al-Qahtani, Wahidah H. Alfaifi, Mohammad Y. Elbehairi, Serag Eldin I. AlJumah, Bayan Ahmed Molecules Article The anticancer activity of terretonin N (1) and butyrolactone I (2), obtained from the thermophilic fungus Aspergillus terreus TM8, was intensively studied against prostate adenocarcinoma (PC-3) and ovary adenocarcinoma (SKOV3) human cell lines. According to this study, both compounds showed potent cytotoxicity towards ovarian adenocarcinoma cells (SKOV3) with IC(50) 1.2 and 0.6 μg/mL, respectively. With respect to metastatic prostate cells (PC-3), the two compounds 1 and 2 showed a significantly promising cytotoxicity effect with IC(50) of 7.4 and 4.5 μg/mL, respectively. The tested fungal metabolites showed higher rates of early and late apoptosis with little or no necrotic apoptotic pathway in all treated prostate adenocarcinoma (PC-3) and ovary adenocarcinoma (SKOV3) human cell lines, respectively. The results reported in this study confirmed the promising biological properties of terretonin N (1) and butyrolactone I (2) as anticancer agents via the induction of cellular apoptosis. However, further studies are needed to elucidate the molecular mechanism by which cellular apoptosis is induced in cancer cells. MDPI 2021-05-10 /pmc/articles/PMC8126039/ /pubmed/34068647 http://dx.doi.org/10.3390/molecules26092816 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
Ghfar, Ayman A.
El-Metwally, Mohammad Magdy
Shaaban, Mohamed
Gabr, Sami A.
Gabr, Nada S.
Diab, Marwa S. M.
Aqel, Ahmad
Habila, Mohamed A.
Al-Qahtani, Wahidah H.
Alfaifi, Mohammad Y.
Elbehairi, Serag Eldin I.
AlJumah, Bayan Ahmed
Production of Terretonin N and Butyrolactone I by Thermophilic Aspergillus terreus TM8 Promoted Apoptosis and Cell Death in Human Prostate and Ovarian Cancer Cells
title Production of Terretonin N and Butyrolactone I by Thermophilic Aspergillus terreus TM8 Promoted Apoptosis and Cell Death in Human Prostate and Ovarian Cancer Cells
title_full Production of Terretonin N and Butyrolactone I by Thermophilic Aspergillus terreus TM8 Promoted Apoptosis and Cell Death in Human Prostate and Ovarian Cancer Cells
title_fullStr Production of Terretonin N and Butyrolactone I by Thermophilic Aspergillus terreus TM8 Promoted Apoptosis and Cell Death in Human Prostate and Ovarian Cancer Cells
title_full_unstemmed Production of Terretonin N and Butyrolactone I by Thermophilic Aspergillus terreus TM8 Promoted Apoptosis and Cell Death in Human Prostate and Ovarian Cancer Cells
title_short Production of Terretonin N and Butyrolactone I by Thermophilic Aspergillus terreus TM8 Promoted Apoptosis and Cell Death in Human Prostate and Ovarian Cancer Cells
title_sort production of terretonin n and butyrolactone i by thermophilic aspergillus terreus tm8 promoted apoptosis and cell death in human prostate and ovarian cancer cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8126039/
https://www.ncbi.nlm.nih.gov/pubmed/34068647
http://dx.doi.org/10.3390/molecules26092816
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