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β-Caryophyllene in the Essential Oil from Chrysanthemum Boreale Induces G(1) Phase Cell Cycle Arrest in Human Lung Cancer Cells
Chrysanthemum boreale is a plant widespread in East Asia, used in folk medicine to treat various disorders, such as pneumonia, colitis, stomatitis, and carbuncle. Whether the essential oil from C. boreale (ECB) and its active constituents have anti-proliferative activities in lung cancer is unknown....
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6832734/ https://www.ncbi.nlm.nih.gov/pubmed/31635244 http://dx.doi.org/10.3390/molecules24203754 |
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author | Chung, Kyung-Sook Hong, Joo Young Lee, Jeong-Hun Lee, Hae-Jun Park, Ji Yeon Choi, Jung-Hye Park, Hee-Juhn Hong, Jongki Lee, Kyung-Tae |
author_facet | Chung, Kyung-Sook Hong, Joo Young Lee, Jeong-Hun Lee, Hae-Jun Park, Ji Yeon Choi, Jung-Hye Park, Hee-Juhn Hong, Jongki Lee, Kyung-Tae |
author_sort | Chung, Kyung-Sook |
collection | PubMed |
description | Chrysanthemum boreale is a plant widespread in East Asia, used in folk medicine to treat various disorders, such as pneumonia, colitis, stomatitis, and carbuncle. Whether the essential oil from C. boreale (ECB) and its active constituents have anti-proliferative activities in lung cancer is unknown. Therefore, we investigated the cytotoxic effects of ECB in A549 and NCI-H358 human lung cancer cells. Culture of A549 and NCI-H358 cells with ECB induced apoptotic cell death, as revealed by an increase in annexin V staining. ECB treatment reduced mitochondrial membrane potential (MMP), disrupted the balance between pro-apoptotic and anti-apoptotic Bcl-2 proteins, and activated caspase-8, -9, and -3, as assessed by western blot analysis. Interestingly, pretreatment with a broad-spectrum caspase inhibitor (z-VAD-fmk) significantly attenuated ECB-induced apoptosis. Furthermore, gas chromatography–mass spectrometry (GC/MS) analysis of ECB identified six compounds. Among them, β-caryophyllene exhibited a potent anti-proliferative effect, and thus was identified as the major active compound. β- Caryophyllene induced G(1) cell cycle arrest by downregulating cyclin D1, cyclin E, cyclin-dependent protein kinase (CDK) -2, -4, and -6, and RB phosphorylation, and by upregulating p21(CIP1/WAF1) and p27(KIP1). These results indicate that β-caryophyllene exerts cytotoxic activity in lung cancer cells through induction of cell cycle arrest. |
format | Online Article Text |
id | pubmed-6832734 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-68327342019-11-25 β-Caryophyllene in the Essential Oil from Chrysanthemum Boreale Induces G(1) Phase Cell Cycle Arrest in Human Lung Cancer Cells Chung, Kyung-Sook Hong, Joo Young Lee, Jeong-Hun Lee, Hae-Jun Park, Ji Yeon Choi, Jung-Hye Park, Hee-Juhn Hong, Jongki Lee, Kyung-Tae Molecules Article Chrysanthemum boreale is a plant widespread in East Asia, used in folk medicine to treat various disorders, such as pneumonia, colitis, stomatitis, and carbuncle. Whether the essential oil from C. boreale (ECB) and its active constituents have anti-proliferative activities in lung cancer is unknown. Therefore, we investigated the cytotoxic effects of ECB in A549 and NCI-H358 human lung cancer cells. Culture of A549 and NCI-H358 cells with ECB induced apoptotic cell death, as revealed by an increase in annexin V staining. ECB treatment reduced mitochondrial membrane potential (MMP), disrupted the balance between pro-apoptotic and anti-apoptotic Bcl-2 proteins, and activated caspase-8, -9, and -3, as assessed by western blot analysis. Interestingly, pretreatment with a broad-spectrum caspase inhibitor (z-VAD-fmk) significantly attenuated ECB-induced apoptosis. Furthermore, gas chromatography–mass spectrometry (GC/MS) analysis of ECB identified six compounds. Among them, β-caryophyllene exhibited a potent anti-proliferative effect, and thus was identified as the major active compound. β- Caryophyllene induced G(1) cell cycle arrest by downregulating cyclin D1, cyclin E, cyclin-dependent protein kinase (CDK) -2, -4, and -6, and RB phosphorylation, and by upregulating p21(CIP1/WAF1) and p27(KIP1). These results indicate that β-caryophyllene exerts cytotoxic activity in lung cancer cells through induction of cell cycle arrest. MDPI 2019-10-18 /pmc/articles/PMC6832734/ /pubmed/31635244 http://dx.doi.org/10.3390/molecules24203754 Text en © 2019 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Chung, Kyung-Sook Hong, Joo Young Lee, Jeong-Hun Lee, Hae-Jun Park, Ji Yeon Choi, Jung-Hye Park, Hee-Juhn Hong, Jongki Lee, Kyung-Tae β-Caryophyllene in the Essential Oil from Chrysanthemum Boreale Induces G(1) Phase Cell Cycle Arrest in Human Lung Cancer Cells |
title | β-Caryophyllene in the Essential Oil from Chrysanthemum Boreale Induces G(1) Phase Cell Cycle Arrest in Human Lung Cancer Cells |
title_full | β-Caryophyllene in the Essential Oil from Chrysanthemum Boreale Induces G(1) Phase Cell Cycle Arrest in Human Lung Cancer Cells |
title_fullStr | β-Caryophyllene in the Essential Oil from Chrysanthemum Boreale Induces G(1) Phase Cell Cycle Arrest in Human Lung Cancer Cells |
title_full_unstemmed | β-Caryophyllene in the Essential Oil from Chrysanthemum Boreale Induces G(1) Phase Cell Cycle Arrest in Human Lung Cancer Cells |
title_short | β-Caryophyllene in the Essential Oil from Chrysanthemum Boreale Induces G(1) Phase Cell Cycle Arrest in Human Lung Cancer Cells |
title_sort | β-caryophyllene in the essential oil from chrysanthemum boreale induces g(1) phase cell cycle arrest in human lung cancer cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6832734/ https://www.ncbi.nlm.nih.gov/pubmed/31635244 http://dx.doi.org/10.3390/molecules24203754 |
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