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An In Vitro Anti-Cancer Activity of Ocimum tenuiflorum Essential Oil by Inducing Apoptosis in Human Gastric Cancer Cell Line

Background and Objectives: The effects of Ocimum tenuiflorum essential oil (OTEO) against gastric cancer remain unknown and merit investigation. Materials and Methods: In the present study, the anti-cancer activity of OTEO was examined in a human gastric cancer cell line (AGS). After OTEO treatment,...

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Autores principales: Boonyanugomol, Wongwarut, Rukseree, Kamolchanok, Prapatpong, Pornpan, Reamtong, Onrapak, Baik, Seung-Chul, Jung, Myunghwan, Shin, Min-Kyoung, Kang, Hyung-Lyun, Lee, Woo-Kon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8400819/
https://www.ncbi.nlm.nih.gov/pubmed/34440988
http://dx.doi.org/10.3390/medicina57080784
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author Boonyanugomol, Wongwarut
Rukseree, Kamolchanok
Prapatpong, Pornpan
Reamtong, Onrapak
Baik, Seung-Chul
Jung, Myunghwan
Shin, Min-Kyoung
Kang, Hyung-Lyun
Lee, Woo-Kon
author_facet Boonyanugomol, Wongwarut
Rukseree, Kamolchanok
Prapatpong, Pornpan
Reamtong, Onrapak
Baik, Seung-Chul
Jung, Myunghwan
Shin, Min-Kyoung
Kang, Hyung-Lyun
Lee, Woo-Kon
author_sort Boonyanugomol, Wongwarut
collection PubMed
description Background and Objectives: The effects of Ocimum tenuiflorum essential oil (OTEO) against gastric cancer remain unknown and merit investigation. Materials and Methods: In the present study, the anti-cancer activity of OTEO was examined in a human gastric cancer cell line (AGS). After OTEO treatment, AGS cell viability was determined by an MTT assay, and inhibition of metastasis was determined by cell migration and invasion assays. The expression of apoptosis-related genes in treated AGS cells was determined by qRT-PCR. Results: OTEO significantly decreased AGS cell viability in a dose-dependent manner (IC(50) 163.42 µg/mL) and effectively inhibited cell migration and invasion. Morphological examination demonstrated that OTEO induced cell shrinkage, chromatin condensation, and fragmentation, which are considered typical morphologies of apoptotic cell death. Pro-apoptotic genes (TP53, BAX, and BAK) were significantly up-regulated, while anti-apoptotic genes (BCL-2 and BCL-xL) were significantly down-regulated after treatment with OTEO. In addition, significantly increased gene expression was detected for CASP8, CASP9, and CASP3 in AGS cells exposed to OTEO. GC-MS analysis demonstrated that the major compound of OTEO was caryophyllene (25.85%) and α-pinene (11.66%). Conclusions: This in vitro study demonstrates for the first time that OTEO has potential anti-gastric cancer activity and may induce apoptosis in AGS cells through extrinsic and intrinsic pathways.
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spelling pubmed-84008192021-08-29 An In Vitro Anti-Cancer Activity of Ocimum tenuiflorum Essential Oil by Inducing Apoptosis in Human Gastric Cancer Cell Line Boonyanugomol, Wongwarut Rukseree, Kamolchanok Prapatpong, Pornpan Reamtong, Onrapak Baik, Seung-Chul Jung, Myunghwan Shin, Min-Kyoung Kang, Hyung-Lyun Lee, Woo-Kon Medicina (Kaunas) Article Background and Objectives: The effects of Ocimum tenuiflorum essential oil (OTEO) against gastric cancer remain unknown and merit investigation. Materials and Methods: In the present study, the anti-cancer activity of OTEO was examined in a human gastric cancer cell line (AGS). After OTEO treatment, AGS cell viability was determined by an MTT assay, and inhibition of metastasis was determined by cell migration and invasion assays. The expression of apoptosis-related genes in treated AGS cells was determined by qRT-PCR. Results: OTEO significantly decreased AGS cell viability in a dose-dependent manner (IC(50) 163.42 µg/mL) and effectively inhibited cell migration and invasion. Morphological examination demonstrated that OTEO induced cell shrinkage, chromatin condensation, and fragmentation, which are considered typical morphologies of apoptotic cell death. Pro-apoptotic genes (TP53, BAX, and BAK) were significantly up-regulated, while anti-apoptotic genes (BCL-2 and BCL-xL) were significantly down-regulated after treatment with OTEO. In addition, significantly increased gene expression was detected for CASP8, CASP9, and CASP3 in AGS cells exposed to OTEO. GC-MS analysis demonstrated that the major compound of OTEO was caryophyllene (25.85%) and α-pinene (11.66%). Conclusions: This in vitro study demonstrates for the first time that OTEO has potential anti-gastric cancer activity and may induce apoptosis in AGS cells through extrinsic and intrinsic pathways. MDPI 2021-07-30 /pmc/articles/PMC8400819/ /pubmed/34440988 http://dx.doi.org/10.3390/medicina57080784 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
Boonyanugomol, Wongwarut
Rukseree, Kamolchanok
Prapatpong, Pornpan
Reamtong, Onrapak
Baik, Seung-Chul
Jung, Myunghwan
Shin, Min-Kyoung
Kang, Hyung-Lyun
Lee, Woo-Kon
An In Vitro Anti-Cancer Activity of Ocimum tenuiflorum Essential Oil by Inducing Apoptosis in Human Gastric Cancer Cell Line
title An In Vitro Anti-Cancer Activity of Ocimum tenuiflorum Essential Oil by Inducing Apoptosis in Human Gastric Cancer Cell Line
title_full An In Vitro Anti-Cancer Activity of Ocimum tenuiflorum Essential Oil by Inducing Apoptosis in Human Gastric Cancer Cell Line
title_fullStr An In Vitro Anti-Cancer Activity of Ocimum tenuiflorum Essential Oil by Inducing Apoptosis in Human Gastric Cancer Cell Line
title_full_unstemmed An In Vitro Anti-Cancer Activity of Ocimum tenuiflorum Essential Oil by Inducing Apoptosis in Human Gastric Cancer Cell Line
title_short An In Vitro Anti-Cancer Activity of Ocimum tenuiflorum Essential Oil by Inducing Apoptosis in Human Gastric Cancer Cell Line
title_sort in vitro anti-cancer activity of ocimum tenuiflorum essential oil by inducing apoptosis in human gastric cancer cell line
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8400819/
https://www.ncbi.nlm.nih.gov/pubmed/34440988
http://dx.doi.org/10.3390/medicina57080784
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