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Polyphenols Isolated from Allium cepa L. Induces Apoptosis by Induction of p53 and Suppression of Bcl-2 through Inhibiting PI3K/Akt Signaling Pathway in AGS Human Cancer Cells

BACKGROUND: The extract of Allium cepa Linn is commonly used as adjuvant food for cancer therapy. We assumed that it includes a potential source of anti-cancer properties. METHODS: We investigated anti-cancer effects of polyphenols extracted from lyophilized A. cepa Linn (PEAL) in AGS human cancer c...

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Autores principales: Lee, Won Sup, Yi, Sang Mi, Yun, Jeong Won, Jung, Ji Hyun, Kim, Dong Hoon, Kim, Hye Jung, Chang, Seong-Hwan, Kim, GonSup, Ryu, Chung Ho, Shin, Sung Chul, Hong, Soon Chan, Choi, Yung Hyun, Jung, Jin-Myung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Cancer Prevention 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4189478/
https://www.ncbi.nlm.nih.gov/pubmed/25337568
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author Lee, Won Sup
Yi, Sang Mi
Yun, Jeong Won
Jung, Ji Hyun
Kim, Dong Hoon
Kim, Hye Jung
Chang, Seong-Hwan
Kim, GonSup
Ryu, Chung Ho
Shin, Sung Chul
Hong, Soon Chan
Choi, Yung Hyun
Jung, Jin-Myung
author_facet Lee, Won Sup
Yi, Sang Mi
Yun, Jeong Won
Jung, Ji Hyun
Kim, Dong Hoon
Kim, Hye Jung
Chang, Seong-Hwan
Kim, GonSup
Ryu, Chung Ho
Shin, Sung Chul
Hong, Soon Chan
Choi, Yung Hyun
Jung, Jin-Myung
author_sort Lee, Won Sup
collection PubMed
description BACKGROUND: The extract of Allium cepa Linn is commonly used as adjuvant food for cancer therapy. We assumed that it includes a potential source of anti-cancer properties. METHODS: We investigated anti-cancer effects of polyphenols extracted from lyophilized A. cepa Linn (PEAL) in AGS human cancer cells. RESULTS: PEAL inhibited cell growth in a dose-dependent manner. It was related to caspase-dependent apoptosis. We confirmed this finding with annexin V staining. PEAL up-regulated p53 expression, and subsequent Bax induction, down regulated Bcl-2 protein, anti-apoptotic protein. In addition, PEAL suppressed Akt activity and PEAL-induced apoptosis were significantly accentuated with Akt inhibitor (LY294002). CONCLUSIONS: Our data suggested that PEAL induce caspase-dependent apoptosis through mitochondrial pathway by up-regulating p53 protein, and subsequent Bax protein as well as by modulating Bcl-2 protein, and that PEAL induces caspase-dependent apoptosis at least in part through the inhibition of phosphatidylinositol 3-kinase (PI3K)/Akt signaling pathway. This study provides evidence that PEAL might be useful for the treatment of cancer.
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spelling pubmed-41894782014-10-21 Polyphenols Isolated from Allium cepa L. Induces Apoptosis by Induction of p53 and Suppression of Bcl-2 through Inhibiting PI3K/Akt Signaling Pathway in AGS Human Cancer Cells Lee, Won Sup Yi, Sang Mi Yun, Jeong Won Jung, Ji Hyun Kim, Dong Hoon Kim, Hye Jung Chang, Seong-Hwan Kim, GonSup Ryu, Chung Ho Shin, Sung Chul Hong, Soon Chan Choi, Yung Hyun Jung, Jin-Myung J Cancer Prev Original Article BACKGROUND: The extract of Allium cepa Linn is commonly used as adjuvant food for cancer therapy. We assumed that it includes a potential source of anti-cancer properties. METHODS: We investigated anti-cancer effects of polyphenols extracted from lyophilized A. cepa Linn (PEAL) in AGS human cancer cells. RESULTS: PEAL inhibited cell growth in a dose-dependent manner. It was related to caspase-dependent apoptosis. We confirmed this finding with annexin V staining. PEAL up-regulated p53 expression, and subsequent Bax induction, down regulated Bcl-2 protein, anti-apoptotic protein. In addition, PEAL suppressed Akt activity and PEAL-induced apoptosis were significantly accentuated with Akt inhibitor (LY294002). CONCLUSIONS: Our data suggested that PEAL induce caspase-dependent apoptosis through mitochondrial pathway by up-regulating p53 protein, and subsequent Bax protein as well as by modulating Bcl-2 protein, and that PEAL induces caspase-dependent apoptosis at least in part through the inhibition of phosphatidylinositol 3-kinase (PI3K)/Akt signaling pathway. This study provides evidence that PEAL might be useful for the treatment of cancer. Korean Society of Cancer Prevention 2014-03 /pmc/articles/PMC4189478/ /pubmed/25337568 Text en Copyright © 2014 Korean Society of Cancer Prevention This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Lee, Won Sup
Yi, Sang Mi
Yun, Jeong Won
Jung, Ji Hyun
Kim, Dong Hoon
Kim, Hye Jung
Chang, Seong-Hwan
Kim, GonSup
Ryu, Chung Ho
Shin, Sung Chul
Hong, Soon Chan
Choi, Yung Hyun
Jung, Jin-Myung
Polyphenols Isolated from Allium cepa L. Induces Apoptosis by Induction of p53 and Suppression of Bcl-2 through Inhibiting PI3K/Akt Signaling Pathway in AGS Human Cancer Cells
title Polyphenols Isolated from Allium cepa L. Induces Apoptosis by Induction of p53 and Suppression of Bcl-2 through Inhibiting PI3K/Akt Signaling Pathway in AGS Human Cancer Cells
title_full Polyphenols Isolated from Allium cepa L. Induces Apoptosis by Induction of p53 and Suppression of Bcl-2 through Inhibiting PI3K/Akt Signaling Pathway in AGS Human Cancer Cells
title_fullStr Polyphenols Isolated from Allium cepa L. Induces Apoptosis by Induction of p53 and Suppression of Bcl-2 through Inhibiting PI3K/Akt Signaling Pathway in AGS Human Cancer Cells
title_full_unstemmed Polyphenols Isolated from Allium cepa L. Induces Apoptosis by Induction of p53 and Suppression of Bcl-2 through Inhibiting PI3K/Akt Signaling Pathway in AGS Human Cancer Cells
title_short Polyphenols Isolated from Allium cepa L. Induces Apoptosis by Induction of p53 and Suppression of Bcl-2 through Inhibiting PI3K/Akt Signaling Pathway in AGS Human Cancer Cells
title_sort polyphenols isolated from allium cepa l. induces apoptosis by induction of p53 and suppression of bcl-2 through inhibiting pi3k/akt signaling pathway in ags human cancer cells
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4189478/
https://www.ncbi.nlm.nih.gov/pubmed/25337568
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