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Quercetin induced apoptosis of human oral cancer SAS cells through mitochondria and endoplasmic reticulum mediated signaling pathways

Oral cancer is a cause of cancer-associated mortality worldwide and the treatment of oral cancer includes radiation, surgery and chemotherapy. Quercetin is a component from natural plant products and it has been demonstrated that quercetin is able to induce cytotoxic effects through induction of cel...

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Autores principales: Ma, Yi-Shih, Yao, Chien-Ning, Liu, Hsin-Chung, Yu, Fu-Shun, Lin, Jen-Jyh, Lu, Kung-Wen, Liao, Ching-Lung, Chueh, Fu-Shin, Chung, Jing-Gung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6004715/
https://www.ncbi.nlm.nih.gov/pubmed/29928342
http://dx.doi.org/10.3892/ol.2018.8584
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author Ma, Yi-Shih
Yao, Chien-Ning
Liu, Hsin-Chung
Yu, Fu-Shun
Lin, Jen-Jyh
Lu, Kung-Wen
Liao, Ching-Lung
Chueh, Fu-Shin
Chung, Jing-Gung
author_facet Ma, Yi-Shih
Yao, Chien-Ning
Liu, Hsin-Chung
Yu, Fu-Shun
Lin, Jen-Jyh
Lu, Kung-Wen
Liao, Ching-Lung
Chueh, Fu-Shin
Chung, Jing-Gung
author_sort Ma, Yi-Shih
collection PubMed
description Oral cancer is a cause of cancer-associated mortality worldwide and the treatment of oral cancer includes radiation, surgery and chemotherapy. Quercetin is a component from natural plant products and it has been demonstrated that quercetin is able to induce cytotoxic effects through induction of cell apoptosis in a number of human cancer cell lines. However, there is no available information to demonstrate that quercetin is able to induce apoptosis in human oral cancer cells. In the present study, the effect of quercetin on the cell death via the induction of apoptosis in human oral cancer SAS cells was investigated using flow cytometry, Annexin V/propidium iodide (PI) double staining, western blotting and confocal laser microscopy examination, to test for cytotoxic effects at 6–48 h after treatment with quercetin. The rate of cell death increased with the duration of quercetin treatment based on the results of a cell viability assay, increased Annexin V/PI staining, increased reactive oxygen species and Ca(2+) production, decreased the levels of mitochondrial membrane potential (ΔΨ(m)), increased proportion of apoptotic cells and altered levels of apoptosis-associated protein expression in SAS cells. The results from western blotting revealed that quercetin increased Fas, Fas-Ligand, fas-associated protein with death domain and caspase-8, all of which associated with cell surface death receptor. Furthermore, quercetin increased the levels of activating transcription factor (ATF)-6α, ATF-6β and gastrin-releasing peptide-78 which indicated an increase in endoplasm reticulum stress, increased levels of the pro-apoptotic protein BH3 interacting-domain death antagonist, and decreased levels of anti-apoptotic proteins B-cell lymphoma (Bcl) 2 and Bcl-extra large which may have led to the decreases of ΔΨ(m). Additionally, confocal microscopy suggested that quercetin was able to increase the expression levels of cytochrome c, apoptosis-inducing factor and endonuclease G, which are associated with apoptotic pathways. Therefore, it is hypothesized that quercetin may potentially be used as a novel anti-cancer agent for the treatment of oral cancer in future.
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spelling pubmed-60047152018-06-20 Quercetin induced apoptosis of human oral cancer SAS cells through mitochondria and endoplasmic reticulum mediated signaling pathways Ma, Yi-Shih Yao, Chien-Ning Liu, Hsin-Chung Yu, Fu-Shun Lin, Jen-Jyh Lu, Kung-Wen Liao, Ching-Lung Chueh, Fu-Shin Chung, Jing-Gung Oncol Lett Articles Oral cancer is a cause of cancer-associated mortality worldwide and the treatment of oral cancer includes radiation, surgery and chemotherapy. Quercetin is a component from natural plant products and it has been demonstrated that quercetin is able to induce cytotoxic effects through induction of cell apoptosis in a number of human cancer cell lines. However, there is no available information to demonstrate that quercetin is able to induce apoptosis in human oral cancer cells. In the present study, the effect of quercetin on the cell death via the induction of apoptosis in human oral cancer SAS cells was investigated using flow cytometry, Annexin V/propidium iodide (PI) double staining, western blotting and confocal laser microscopy examination, to test for cytotoxic effects at 6–48 h after treatment with quercetin. The rate of cell death increased with the duration of quercetin treatment based on the results of a cell viability assay, increased Annexin V/PI staining, increased reactive oxygen species and Ca(2+) production, decreased the levels of mitochondrial membrane potential (ΔΨ(m)), increased proportion of apoptotic cells and altered levels of apoptosis-associated protein expression in SAS cells. The results from western blotting revealed that quercetin increased Fas, Fas-Ligand, fas-associated protein with death domain and caspase-8, all of which associated with cell surface death receptor. Furthermore, quercetin increased the levels of activating transcription factor (ATF)-6α, ATF-6β and gastrin-releasing peptide-78 which indicated an increase in endoplasm reticulum stress, increased levels of the pro-apoptotic protein BH3 interacting-domain death antagonist, and decreased levels of anti-apoptotic proteins B-cell lymphoma (Bcl) 2 and Bcl-extra large which may have led to the decreases of ΔΨ(m). Additionally, confocal microscopy suggested that quercetin was able to increase the expression levels of cytochrome c, apoptosis-inducing factor and endonuclease G, which are associated with apoptotic pathways. Therefore, it is hypothesized that quercetin may potentially be used as a novel anti-cancer agent for the treatment of oral cancer in future. D.A. Spandidos 2018-06 2018-04-26 /pmc/articles/PMC6004715/ /pubmed/29928342 http://dx.doi.org/10.3892/ol.2018.8584 Text en Copyright: © Ma et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Ma, Yi-Shih
Yao, Chien-Ning
Liu, Hsin-Chung
Yu, Fu-Shun
Lin, Jen-Jyh
Lu, Kung-Wen
Liao, Ching-Lung
Chueh, Fu-Shin
Chung, Jing-Gung
Quercetin induced apoptosis of human oral cancer SAS cells through mitochondria and endoplasmic reticulum mediated signaling pathways
title Quercetin induced apoptosis of human oral cancer SAS cells through mitochondria and endoplasmic reticulum mediated signaling pathways
title_full Quercetin induced apoptosis of human oral cancer SAS cells through mitochondria and endoplasmic reticulum mediated signaling pathways
title_fullStr Quercetin induced apoptosis of human oral cancer SAS cells through mitochondria and endoplasmic reticulum mediated signaling pathways
title_full_unstemmed Quercetin induced apoptosis of human oral cancer SAS cells through mitochondria and endoplasmic reticulum mediated signaling pathways
title_short Quercetin induced apoptosis of human oral cancer SAS cells through mitochondria and endoplasmic reticulum mediated signaling pathways
title_sort quercetin induced apoptosis of human oral cancer sas cells through mitochondria and endoplasmic reticulum mediated signaling pathways
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6004715/
https://www.ncbi.nlm.nih.gov/pubmed/29928342
http://dx.doi.org/10.3892/ol.2018.8584
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