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βcaryophyllene oxide induces apoptosis and inhibits proliferation of A549 lung cancer cells
One of the most common cancers that result in death is lung cancer. There is new hope in the fight against lung cancer thanks to the chemopreventive properties of natural dietary substances like β-caryophyllene oxide (CPO), and research is currently being done to test this theory. CPO, a sesquiterpe...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer US
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10220129/ https://www.ncbi.nlm.nih.gov/pubmed/37233859 http://dx.doi.org/10.1007/s12032-023-02022-9 |
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author | Shabana, Sameh M. Gad, Nahla S. Othman, Azza I. Mohamed, Aly Fahmy El-Missiry, Mohamed Amr |
author_facet | Shabana, Sameh M. Gad, Nahla S. Othman, Azza I. Mohamed, Aly Fahmy El-Missiry, Mohamed Amr |
author_sort | Shabana, Sameh M. |
collection | PubMed |
description | One of the most common cancers that result in death is lung cancer. There is new hope in the fight against lung cancer thanks to the chemopreventive properties of natural dietary substances like β-caryophyllene oxide (CPO), and research is currently being done to test this theory. CPO, a sesquiterpene isolated from medicinal plant essential oils, inhibits carcinogenesis and has been effective in treating many cancers. This study examined how CPO affected proliferation of human lung cancer A549 cells. CPO was found to have an inhibitory concentration (IC50) of 124.1 g/ml. The proliferative markers Ki67 and PCNA were significantly inhibited after cells were treated with CPO at a concentration of 50 g/ml compared to controls. CPO-treated cells expressed more P21, P53, and DNA strand breaks than controls. This was accompanied by a significant cell cycle arrest in the S and G2/M phases. In treated A549 cells, this was also associated with a significant induction of apoptosis, as shown by the upregulation of the expression of caspases 3, 7, and 9, as well as Bax, and the downregulation of Bcl-2. Furthermore, the redox status of treated A549 cells revealed a marked rise in GSH and GPx activity levels and a decline in 4-HNE levels, indicating low oxidative stress following CPO treatment of A549 cells. In conclusion, cell cycle arrest and apoptosis, which are unrelated to oxidative stress, were the mechanisms by which CPO reduced cancer lung cell growth. This finding might be a potential therapeutic target for the treatment of lung cancer. GRAPHICAL ABSTRACT: Hypothetical scheme of CPO anticancer effects (mechanism of signaling) in A549 cells; in vitro. CPO treatment increases expression of p21, p53 and DNA fragmentation. These events cause arrest of cell cycle which was associated with significant induction in apoptosis via increase expression of caspases (-3,-7,-9), and Bax and downregulation of Bcl-2. [Image: see text] |
format | Online Article Text |
id | pubmed-10220129 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-102201292023-05-28 βcaryophyllene oxide induces apoptosis and inhibits proliferation of A549 lung cancer cells Shabana, Sameh M. Gad, Nahla S. Othman, Azza I. Mohamed, Aly Fahmy El-Missiry, Mohamed Amr Med Oncol Original Paper One of the most common cancers that result in death is lung cancer. There is new hope in the fight against lung cancer thanks to the chemopreventive properties of natural dietary substances like β-caryophyllene oxide (CPO), and research is currently being done to test this theory. CPO, a sesquiterpene isolated from medicinal plant essential oils, inhibits carcinogenesis and has been effective in treating many cancers. This study examined how CPO affected proliferation of human lung cancer A549 cells. CPO was found to have an inhibitory concentration (IC50) of 124.1 g/ml. The proliferative markers Ki67 and PCNA were significantly inhibited after cells were treated with CPO at a concentration of 50 g/ml compared to controls. CPO-treated cells expressed more P21, P53, and DNA strand breaks than controls. This was accompanied by a significant cell cycle arrest in the S and G2/M phases. In treated A549 cells, this was also associated with a significant induction of apoptosis, as shown by the upregulation of the expression of caspases 3, 7, and 9, as well as Bax, and the downregulation of Bcl-2. Furthermore, the redox status of treated A549 cells revealed a marked rise in GSH and GPx activity levels and a decline in 4-HNE levels, indicating low oxidative stress following CPO treatment of A549 cells. In conclusion, cell cycle arrest and apoptosis, which are unrelated to oxidative stress, were the mechanisms by which CPO reduced cancer lung cell growth. This finding might be a potential therapeutic target for the treatment of lung cancer. GRAPHICAL ABSTRACT: Hypothetical scheme of CPO anticancer effects (mechanism of signaling) in A549 cells; in vitro. CPO treatment increases expression of p21, p53 and DNA fragmentation. These events cause arrest of cell cycle which was associated with significant induction in apoptosis via increase expression of caspases (-3,-7,-9), and Bax and downregulation of Bcl-2. [Image: see text] Springer US 2023-05-26 2023 /pmc/articles/PMC10220129/ /pubmed/37233859 http://dx.doi.org/10.1007/s12032-023-02022-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Paper Shabana, Sameh M. Gad, Nahla S. Othman, Azza I. Mohamed, Aly Fahmy El-Missiry, Mohamed Amr βcaryophyllene oxide induces apoptosis and inhibits proliferation of A549 lung cancer cells |
title | βcaryophyllene oxide induces apoptosis and inhibits proliferation of A549 lung cancer cells |
title_full | βcaryophyllene oxide induces apoptosis and inhibits proliferation of A549 lung cancer cells |
title_fullStr | βcaryophyllene oxide induces apoptosis and inhibits proliferation of A549 lung cancer cells |
title_full_unstemmed | βcaryophyllene oxide induces apoptosis and inhibits proliferation of A549 lung cancer cells |
title_short | βcaryophyllene oxide induces apoptosis and inhibits proliferation of A549 lung cancer cells |
title_sort | βcaryophyllene oxide induces apoptosis and inhibits proliferation of a549 lung cancer cells |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10220129/ https://www.ncbi.nlm.nih.gov/pubmed/37233859 http://dx.doi.org/10.1007/s12032-023-02022-9 |
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