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Deguelin exerts anticancer activity of human gastric cancer MGC-803 and MKN-45 cells in vitro

During the pathogenesis of gastric cancer, Akt signaling is considered as a pivotal inducer of gastric cancer development. Here we report the identification of anticancer activities of deguelin, a natural agent that inhibits Akt signaling. When applied to MGC-803 and MKN-45 cells, deguelin suppresse...

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Detalles Bibliográficos
Autores principales: Kang, Wen, Zheng, Xiao, Wang, Ping, Guo, Shanyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5881843/
https://www.ncbi.nlm.nih.gov/pubmed/29512685
http://dx.doi.org/10.3892/ijmm.2018.3532
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author Kang, Wen
Zheng, Xiao
Wang, Ping
Guo, Shanyu
author_facet Kang, Wen
Zheng, Xiao
Wang, Ping
Guo, Shanyu
author_sort Kang, Wen
collection PubMed
description During the pathogenesis of gastric cancer, Akt signaling is considered as a pivotal inducer of gastric cancer development. Here we report the identification of anticancer activities of deguelin, a natural agent that inhibits Akt signaling. When applied to MGC-803 and MKN-45 cells, deguelin suppressed the proliferation and arrested cell cycle by p21-mediated inhibition of cyclin E. We further present in vitro evidence that deguelin promoted apoptosis of cancer cells by decreasing the phospho-Akt signaling and affecting expression of the apoptosis-associated genes Bax and Bcl-2. Additionally, deguelin was found to suppress the migration and invasion of gastric cancer cells. Taken together, these results indicated that deguelin exerted anticancer activity of human gastric cancer MGC-803 and MKN-45 cells in vitro.
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spelling pubmed-58818432018-04-12 Deguelin exerts anticancer activity of human gastric cancer MGC-803 and MKN-45 cells in vitro Kang, Wen Zheng, Xiao Wang, Ping Guo, Shanyu Int J Mol Med Articles During the pathogenesis of gastric cancer, Akt signaling is considered as a pivotal inducer of gastric cancer development. Here we report the identification of anticancer activities of deguelin, a natural agent that inhibits Akt signaling. When applied to MGC-803 and MKN-45 cells, deguelin suppressed the proliferation and arrested cell cycle by p21-mediated inhibition of cyclin E. We further present in vitro evidence that deguelin promoted apoptosis of cancer cells by decreasing the phospho-Akt signaling and affecting expression of the apoptosis-associated genes Bax and Bcl-2. Additionally, deguelin was found to suppress the migration and invasion of gastric cancer cells. Taken together, these results indicated that deguelin exerted anticancer activity of human gastric cancer MGC-803 and MKN-45 cells in vitro. D.A. Spandidos 2018-06 2018-03-05 /pmc/articles/PMC5881843/ /pubmed/29512685 http://dx.doi.org/10.3892/ijmm.2018.3532 Text en Copyright: © Kang 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
Kang, Wen
Zheng, Xiao
Wang, Ping
Guo, Shanyu
Deguelin exerts anticancer activity of human gastric cancer MGC-803 and MKN-45 cells in vitro
title Deguelin exerts anticancer activity of human gastric cancer MGC-803 and MKN-45 cells in vitro
title_full Deguelin exerts anticancer activity of human gastric cancer MGC-803 and MKN-45 cells in vitro
title_fullStr Deguelin exerts anticancer activity of human gastric cancer MGC-803 and MKN-45 cells in vitro
title_full_unstemmed Deguelin exerts anticancer activity of human gastric cancer MGC-803 and MKN-45 cells in vitro
title_short Deguelin exerts anticancer activity of human gastric cancer MGC-803 and MKN-45 cells in vitro
title_sort deguelin exerts anticancer activity of human gastric cancer mgc-803 and mkn-45 cells in vitro
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5881843/
https://www.ncbi.nlm.nih.gov/pubmed/29512685
http://dx.doi.org/10.3892/ijmm.2018.3532
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