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INHIBITORY EFFECT OF LYCOPENE AGAINST THE GROWTH OF HUMAN GASTRIC CANCER CELLS

BACKGROUND: The aim of this study was to investigate the anti-proliferative effect of Lycopene on HGC-27 cells. MATERIALS AND METHODS: HGC-27 cells were treated with varying concentration lycopene for 24, 48, 72 h. The cell growth inhibition was analyzed by MTT. Western blotting was used to indicate...

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Detalles Bibliográficos
Autores principales: Zhou, ShenKang, Zhang, RuiLi, Bi, TieNan, Lu, Yong, Jiang, LiangXian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: African Traditional Herbal Medicine Supporters Initiative (ATHMSI) 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5566143/
https://www.ncbi.nlm.nih.gov/pubmed/28852735
http://dx.doi.org/10.21010/ajtcam.v13i4.24
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author Zhou, ShenKang
Zhang, RuiLi
Bi, TieNan
Lu, Yong
Jiang, LiangXian
author_facet Zhou, ShenKang
Zhang, RuiLi
Bi, TieNan
Lu, Yong
Jiang, LiangXian
author_sort Zhou, ShenKang
collection PubMed
description BACKGROUND: The aim of this study was to investigate the anti-proliferative effect of Lycopene on HGC-27 cells. MATERIALS AND METHODS: HGC-27 cells were treated with varying concentration lycopene for 24, 48, 72 h. The cell growth inhibition was analyzed by MTT. Western blotting was used to indicate changes in the levels of LC3-I, LC3-II, ERK (extracellular signal-regulated protein kinase) and phosphorylation-ERK (p-ERK). RESULTS: Lycopene displayed antiproliferative activity in HGC-27 cell lines. Western blotting showed that Lycopene significantly enhanced LC3-I, p-ERK proteins expression. In gastric cancer nude mice model, lycopene treatment significantly decreased tumour weight. These findings indicated that lycopene treatment induces the anti-proliferation of HGC-27 cells. CONCLUSION: Lycopene treatment inhibited HGC-27 cells growth by activating ERK.
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spelling pubmed-55661432017-08-29 INHIBITORY EFFECT OF LYCOPENE AGAINST THE GROWTH OF HUMAN GASTRIC CANCER CELLS Zhou, ShenKang Zhang, RuiLi Bi, TieNan Lu, Yong Jiang, LiangXian Afr J Tradit Complement Altern Med Article BACKGROUND: The aim of this study was to investigate the anti-proliferative effect of Lycopene on HGC-27 cells. MATERIALS AND METHODS: HGC-27 cells were treated with varying concentration lycopene for 24, 48, 72 h. The cell growth inhibition was analyzed by MTT. Western blotting was used to indicate changes in the levels of LC3-I, LC3-II, ERK (extracellular signal-regulated protein kinase) and phosphorylation-ERK (p-ERK). RESULTS: Lycopene displayed antiproliferative activity in HGC-27 cell lines. Western blotting showed that Lycopene significantly enhanced LC3-I, p-ERK proteins expression. In gastric cancer nude mice model, lycopene treatment significantly decreased tumour weight. These findings indicated that lycopene treatment induces the anti-proliferation of HGC-27 cells. CONCLUSION: Lycopene treatment inhibited HGC-27 cells growth by activating ERK. African Traditional Herbal Medicine Supporters Initiative (ATHMSI) 2016-07-03 /pmc/articles/PMC5566143/ /pubmed/28852735 http://dx.doi.org/10.21010/ajtcam.v13i4.24 Text en Copyright: © 2016 Afr. J. Traditional Complementary and Alternative Medicines http://creativecommons.org/licenses/CC-BY/4.0 This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License
spellingShingle Article
Zhou, ShenKang
Zhang, RuiLi
Bi, TieNan
Lu, Yong
Jiang, LiangXian
INHIBITORY EFFECT OF LYCOPENE AGAINST THE GROWTH OF HUMAN GASTRIC CANCER CELLS
title INHIBITORY EFFECT OF LYCOPENE AGAINST THE GROWTH OF HUMAN GASTRIC CANCER CELLS
title_full INHIBITORY EFFECT OF LYCOPENE AGAINST THE GROWTH OF HUMAN GASTRIC CANCER CELLS
title_fullStr INHIBITORY EFFECT OF LYCOPENE AGAINST THE GROWTH OF HUMAN GASTRIC CANCER CELLS
title_full_unstemmed INHIBITORY EFFECT OF LYCOPENE AGAINST THE GROWTH OF HUMAN GASTRIC CANCER CELLS
title_short INHIBITORY EFFECT OF LYCOPENE AGAINST THE GROWTH OF HUMAN GASTRIC CANCER CELLS
title_sort inhibitory effect of lycopene against the growth of human gastric cancer cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5566143/
https://www.ncbi.nlm.nih.gov/pubmed/28852735
http://dx.doi.org/10.21010/ajtcam.v13i4.24
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