4.4 Article

β-caryophyllene oxide induces apoptosis and inhibits proliferation of A549 lung cancer cells

Journal

MEDICAL ONCOLOGY
Volume 40, Issue 7, Pages -

Publisher

HUMANA PRESS INC
DOI: 10.1007/s12032-023-02022-9

Keywords

Lung cancer; Essential oils; beta-caryophyllene oxide; Apoptosis; Cell cycle arrest; Oxidative stress

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Research is being conducted to test the chemopreventive properties of natural dietary substance beta-caryophyllene oxide (CPO) against lung cancer. CPO inhibits proliferation of lung cancer cells and induces cell cycle arrest and apoptosis, which could be a potential therapeutic target for lung cancer treatment.
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 beta-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. [GRAPHICS]

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