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A bioactive compound isolated from Duku ( Lansium domesticum Corr) fruit peels exhibits cytotoxicity against T47D cell line
Background: Breast cancer is a major health problem for women globally. Many attempts have been promoted to cure cancer by finding new anticancer medicines from natural resources. Despite the richness of biodiversity discovered, there are some natural resources that remain unexplored. Fruit peels of...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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F1000 Research Limited
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8185580/ https://www.ncbi.nlm.nih.gov/pubmed/34136135 http://dx.doi.org/10.12688/f1000research.21072.2 |
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author | Fadhilah, Khusnul Wahyuono, Subagus Astuti, Puji |
author_facet | Fadhilah, Khusnul Wahyuono, Subagus Astuti, Puji |
author_sort | Fadhilah, Khusnul |
collection | PubMed |
description | Background: Breast cancer is a major health problem for women globally. Many attempts have been promoted to cure cancer by finding new anticancer medicines from natural resources. Despite the richness of biodiversity discovered, there are some natural resources that remain unexplored. Fruit peels of Duku ( Lansium domesticum Corr.) are rich with compounds that may have the potential to be developed as anticancer drugs. This study aimed to isolate cytotoxic compounds from the fruit peels of L. domesticum and assess their cytotoxic nature against T47D cells. Methods: Powdered peels were macerated with ethyl acetate and the filtrate was evaporated to give EtOAc extract A. Dried extract A was triturated with n-hexane to give n-hexane soluble fraction B and insoluble fraction C. The cytotoxic nature of these three samples were assessed using MTT assay using T47D cells and doxorubicin as a control. Results: Fraction C that showed the smallest IC50 (25.56 ± 0.64μg/mL) value compared to extract A and fraction B. Fraction C was further fractionated by vacuum liquid chromatography to give 6 subfractions. Subfraction 2 showed a single compound based on thin layer chromatography, and this compound was identified as Lamesticumin A on the basis of its spectroscopic data. Lamesticumin A demonstrated cytotoxic activity against T47D cell lines with an IC (50) value of 15.68 ± 0.30µg/mL. Conclusions: Further research is needed to investigate the potential of the natural compound Lamesticumin A derived from L. domesticum fruit peel as an anticancer therapy. |
format | Online Article Text |
id | pubmed-8185580 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | F1000 Research Limited |
record_format | MEDLINE/PubMed |
spelling | pubmed-81855802021-06-15 A bioactive compound isolated from Duku ( Lansium domesticum Corr) fruit peels exhibits cytotoxicity against T47D cell line Fadhilah, Khusnul Wahyuono, Subagus Astuti, Puji F1000Res Research Article Background: Breast cancer is a major health problem for women globally. Many attempts have been promoted to cure cancer by finding new anticancer medicines from natural resources. Despite the richness of biodiversity discovered, there are some natural resources that remain unexplored. Fruit peels of Duku ( Lansium domesticum Corr.) are rich with compounds that may have the potential to be developed as anticancer drugs. This study aimed to isolate cytotoxic compounds from the fruit peels of L. domesticum and assess their cytotoxic nature against T47D cells. Methods: Powdered peels were macerated with ethyl acetate and the filtrate was evaporated to give EtOAc extract A. Dried extract A was triturated with n-hexane to give n-hexane soluble fraction B and insoluble fraction C. The cytotoxic nature of these three samples were assessed using MTT assay using T47D cells and doxorubicin as a control. Results: Fraction C that showed the smallest IC50 (25.56 ± 0.64μg/mL) value compared to extract A and fraction B. Fraction C was further fractionated by vacuum liquid chromatography to give 6 subfractions. Subfraction 2 showed a single compound based on thin layer chromatography, and this compound was identified as Lamesticumin A on the basis of its spectroscopic data. Lamesticumin A demonstrated cytotoxic activity against T47D cell lines with an IC (50) value of 15.68 ± 0.30µg/mL. Conclusions: Further research is needed to investigate the potential of the natural compound Lamesticumin A derived from L. domesticum fruit peel as an anticancer therapy. F1000 Research Limited 2021-04-23 /pmc/articles/PMC8185580/ /pubmed/34136135 http://dx.doi.org/10.12688/f1000research.21072.2 Text en Copyright: © 2021 Fadhilah K et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Fadhilah, Khusnul Wahyuono, Subagus Astuti, Puji A bioactive compound isolated from Duku ( Lansium domesticum Corr) fruit peels exhibits cytotoxicity against T47D cell line |
title | A bioactive compound isolated from Duku (
Lansium domesticum Corr) fruit peels exhibits cytotoxicity against T47D cell line |
title_full | A bioactive compound isolated from Duku (
Lansium domesticum Corr) fruit peels exhibits cytotoxicity against T47D cell line |
title_fullStr | A bioactive compound isolated from Duku (
Lansium domesticum Corr) fruit peels exhibits cytotoxicity against T47D cell line |
title_full_unstemmed | A bioactive compound isolated from Duku (
Lansium domesticum Corr) fruit peels exhibits cytotoxicity against T47D cell line |
title_short | A bioactive compound isolated from Duku (
Lansium domesticum Corr) fruit peels exhibits cytotoxicity against T47D cell line |
title_sort | bioactive compound isolated from duku (
lansium domesticum corr) fruit peels exhibits cytotoxicity against t47d cell line |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8185580/ https://www.ncbi.nlm.nih.gov/pubmed/34136135 http://dx.doi.org/10.12688/f1000research.21072.2 |
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