Cargando…

Berberine displays antitumor activity in esophageal cancer cells in vitro

AIM: To investigate the effects of berberine on esophageal cancer (EC) cells and its molecular mechanisms. METHODS: Human esophageal squamous cell carcinoma cell line KYSE-70 and esophageal adenocarcinoma cell line SKGT4 were used. The effects of berberine on cell proliferation were evaluated using...

Descripción completa

Detalles Bibliográficos
Autores principales: Jiang, Shu-Xian, Qi, Bo, Yao, Wen-Jian, Gu, Cheng-Wei, Wei, Xiu-Feng, Zhao, Yi, Liu, Yu-Zhen, Zhao, Bao-Sheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5394514/
https://www.ncbi.nlm.nih.gov/pubmed/28465635
http://dx.doi.org/10.3748/wjg.v23.i14.2511
_version_ 1783229743634579456
author Jiang, Shu-Xian
Qi, Bo
Yao, Wen-Jian
Gu, Cheng-Wei
Wei, Xiu-Feng
Zhao, Yi
Liu, Yu-Zhen
Zhao, Bao-Sheng
author_facet Jiang, Shu-Xian
Qi, Bo
Yao, Wen-Jian
Gu, Cheng-Wei
Wei, Xiu-Feng
Zhao, Yi
Liu, Yu-Zhen
Zhao, Bao-Sheng
author_sort Jiang, Shu-Xian
collection PubMed
description AIM: To investigate the effects of berberine on esophageal cancer (EC) cells and its molecular mechanisms. METHODS: Human esophageal squamous cell carcinoma cell line KYSE-70 and esophageal adenocarcinoma cell line SKGT4 were used. The effects of berberine on cell proliferation were evaluated using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. For cell cycle progression, KYSE-70 cells were stained with propidium iodide (PI) staining buffer (10 mg/mL PI and 100 mg/mL RNase A) for 30 min and cell cycle was analyzed using a BD FACSCalibur flow cytometer. For apoptosis assay, cells were stained with an Annexin V-FITC/PI apoptosis detection kit. The rate of apoptotic cells was analyzed using a dual laser flow cytometer and estimated using BD ModFit software. Levels of proteins related to cell cycle and apoptosis were examined by western blotting. RESULTS: Berberine treatment resulted in growth inhibition of KYSE-70 and SKGT4 cells in a dose-dependent and time-dependent manner. KYSE-70 cells were more susceptible to the inhibitory activities of berberine than SKGT4 cells were. In KYSE-70 cells treated with 50 μmol/L berberine for 48 h, the number of cells in G(2)/M phase (25.94% ± 5.01%) was significantly higher than that in the control group (9.77% ± 1.28%, P < 0.01), and berberine treatment resulted in p21 up-regulation in KYSE-70 cells. Flow cytometric analyses showed that berberine significantly augmented the KYSE-70 apoptotic population at 12 and 24 h post-treatment, when compared with control cells (0.83% vs 43.78% at 12 h, P < 0.05; 0.15% vs 81.86% at 24 h, P < 0.01), and berberine-induced apoptotic effect was stronger at 24 h compared with 12 h. Western blotting showed that berberine inhibited the phosphorylation of Akt, mammalian target of rapamycin and p70S6K, and enhanced AMP-activated protein kinase phosphorylation in a sustained manner. CONCLUSION: Berberine is an inhibitor of human EC cell growth and could be considered as a potential drug for the treatment of EC patients.
format Online
Article
Text
id pubmed-5394514
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Baishideng Publishing Group Inc
record_format MEDLINE/PubMed
spelling pubmed-53945142017-05-02 Berberine displays antitumor activity in esophageal cancer cells in vitro Jiang, Shu-Xian Qi, Bo Yao, Wen-Jian Gu, Cheng-Wei Wei, Xiu-Feng Zhao, Yi Liu, Yu-Zhen Zhao, Bao-Sheng World J Gastroenterol Basic Study AIM: To investigate the effects of berberine on esophageal cancer (EC) cells and its molecular mechanisms. METHODS: Human esophageal squamous cell carcinoma cell line KYSE-70 and esophageal adenocarcinoma cell line SKGT4 were used. The effects of berberine on cell proliferation were evaluated using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. For cell cycle progression, KYSE-70 cells were stained with propidium iodide (PI) staining buffer (10 mg/mL PI and 100 mg/mL RNase A) for 30 min and cell cycle was analyzed using a BD FACSCalibur flow cytometer. For apoptosis assay, cells were stained with an Annexin V-FITC/PI apoptosis detection kit. The rate of apoptotic cells was analyzed using a dual laser flow cytometer and estimated using BD ModFit software. Levels of proteins related to cell cycle and apoptosis were examined by western blotting. RESULTS: Berberine treatment resulted in growth inhibition of KYSE-70 and SKGT4 cells in a dose-dependent and time-dependent manner. KYSE-70 cells were more susceptible to the inhibitory activities of berberine than SKGT4 cells were. In KYSE-70 cells treated with 50 μmol/L berberine for 48 h, the number of cells in G(2)/M phase (25.94% ± 5.01%) was significantly higher than that in the control group (9.77% ± 1.28%, P < 0.01), and berberine treatment resulted in p21 up-regulation in KYSE-70 cells. Flow cytometric analyses showed that berberine significantly augmented the KYSE-70 apoptotic population at 12 and 24 h post-treatment, when compared with control cells (0.83% vs 43.78% at 12 h, P < 0.05; 0.15% vs 81.86% at 24 h, P < 0.01), and berberine-induced apoptotic effect was stronger at 24 h compared with 12 h. Western blotting showed that berberine inhibited the phosphorylation of Akt, mammalian target of rapamycin and p70S6K, and enhanced AMP-activated protein kinase phosphorylation in a sustained manner. CONCLUSION: Berberine is an inhibitor of human EC cell growth and could be considered as a potential drug for the treatment of EC patients. Baishideng Publishing Group Inc 2017-04-14 2017-04-14 /pmc/articles/PMC5394514/ /pubmed/28465635 http://dx.doi.org/10.3748/wjg.v23.i14.2511 Text en ©The Author(s) 2017. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Basic Study
Jiang, Shu-Xian
Qi, Bo
Yao, Wen-Jian
Gu, Cheng-Wei
Wei, Xiu-Feng
Zhao, Yi
Liu, Yu-Zhen
Zhao, Bao-Sheng
Berberine displays antitumor activity in esophageal cancer cells in vitro
title Berberine displays antitumor activity in esophageal cancer cells in vitro
title_full Berberine displays antitumor activity in esophageal cancer cells in vitro
title_fullStr Berberine displays antitumor activity in esophageal cancer cells in vitro
title_full_unstemmed Berberine displays antitumor activity in esophageal cancer cells in vitro
title_short Berberine displays antitumor activity in esophageal cancer cells in vitro
title_sort berberine displays antitumor activity in esophageal cancer cells in vitro
topic Basic Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5394514/
https://www.ncbi.nlm.nih.gov/pubmed/28465635
http://dx.doi.org/10.3748/wjg.v23.i14.2511
work_keys_str_mv AT jiangshuxian berberinedisplaysantitumoractivityinesophagealcancercellsinvitro
AT qibo berberinedisplaysantitumoractivityinesophagealcancercellsinvitro
AT yaowenjian berberinedisplaysantitumoractivityinesophagealcancercellsinvitro
AT guchengwei berberinedisplaysantitumoractivityinesophagealcancercellsinvitro
AT weixiufeng berberinedisplaysantitumoractivityinesophagealcancercellsinvitro
AT zhaoyi berberinedisplaysantitumoractivityinesophagealcancercellsinvitro
AT liuyuzhen berberinedisplaysantitumoractivityinesophagealcancercellsinvitro
AT zhaobaosheng berberinedisplaysantitumoractivityinesophagealcancercellsinvitro