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Econazole nitrate inhibits PI3K activity and promotes apoptosis in lung cancer cells

The phosphatidylinositol-3-kinase (PI3K)/AKT signaling pathway plays a pivotal role in many cellular processes, including the proliferation, survival and differentiation of lung cancer cells. Thus, PI3K is a promising therapeutic target for lung cancer treatment. In this study, we applied free and o...

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Autores principales: Dong, Chao, Yang, Runxiang, Li, Hongjian, Ke, Kunbin, Luo, Chunxiang, Yang, Fang, Shi, Xi-Nan, Zhu, Ying, Liu, Xu, Wong, Man-Hon, Lin, Guimiao, Wang, Xiaomei, Leung, Kwong-Sak, Kung, Hsiang-Fu, Chen, Ceshi, Lin, Marie Chia-mi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5740072/
https://www.ncbi.nlm.nih.gov/pubmed/29269744
http://dx.doi.org/10.1038/s41598-017-18178-0
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author Dong, Chao
Yang, Runxiang
Li, Hongjian
Ke, Kunbin
Luo, Chunxiang
Yang, Fang
Shi, Xi-Nan
Zhu, Ying
Liu, Xu
Wong, Man-Hon
Lin, Guimiao
Wang, Xiaomei
Leung, Kwong-Sak
Kung, Hsiang-Fu
Chen, Ceshi
Lin, Marie Chia-mi
author_facet Dong, Chao
Yang, Runxiang
Li, Hongjian
Ke, Kunbin
Luo, Chunxiang
Yang, Fang
Shi, Xi-Nan
Zhu, Ying
Liu, Xu
Wong, Man-Hon
Lin, Guimiao
Wang, Xiaomei
Leung, Kwong-Sak
Kung, Hsiang-Fu
Chen, Ceshi
Lin, Marie Chia-mi
author_sort Dong, Chao
collection PubMed
description The phosphatidylinositol-3-kinase (PI3K)/AKT signaling pathway plays a pivotal role in many cellular processes, including the proliferation, survival and differentiation of lung cancer cells. Thus, PI3K is a promising therapeutic target for lung cancer treatment. In this study, we applied free and open-source protein-ligand docking software, screened 3167 FDA-approved small molecules, and identified putative PI3Kα inhibitors. Among them, econazole nitrate, an antifungal agent, exhibited the highest activity in decreasing cell viability in pathological types of NSCLC cell lines, including H661 (large cell lung cancer) and A549 (adenocarcinoma). Econazole decreased the protein levels of p-AKT and Bcl-2, but had no effect on the phosphorylation level of ERK. It inhibited cell growth and promote apoptosis in a dose-dependent manner. Furthermore, the combination of econazole and cisplatin exhibited additive and synergistic effects in the H661 and A549 lung cancer cell lines, respectively. Finally, we demonstrated that econazole significantly suppressed A549 tumor growth in nude mice. Our findings suggest that econazole is a new PI3K inhibitor and a potential drug that can be used in lung cancer treatment alone or in combination with cisplatin.
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spelling pubmed-57400722018-01-03 Econazole nitrate inhibits PI3K activity and promotes apoptosis in lung cancer cells Dong, Chao Yang, Runxiang Li, Hongjian Ke, Kunbin Luo, Chunxiang Yang, Fang Shi, Xi-Nan Zhu, Ying Liu, Xu Wong, Man-Hon Lin, Guimiao Wang, Xiaomei Leung, Kwong-Sak Kung, Hsiang-Fu Chen, Ceshi Lin, Marie Chia-mi Sci Rep Article The phosphatidylinositol-3-kinase (PI3K)/AKT signaling pathway plays a pivotal role in many cellular processes, including the proliferation, survival and differentiation of lung cancer cells. Thus, PI3K is a promising therapeutic target for lung cancer treatment. In this study, we applied free and open-source protein-ligand docking software, screened 3167 FDA-approved small molecules, and identified putative PI3Kα inhibitors. Among them, econazole nitrate, an antifungal agent, exhibited the highest activity in decreasing cell viability in pathological types of NSCLC cell lines, including H661 (large cell lung cancer) and A549 (adenocarcinoma). Econazole decreased the protein levels of p-AKT and Bcl-2, but had no effect on the phosphorylation level of ERK. It inhibited cell growth and promote apoptosis in a dose-dependent manner. Furthermore, the combination of econazole and cisplatin exhibited additive and synergistic effects in the H661 and A549 lung cancer cell lines, respectively. Finally, we demonstrated that econazole significantly suppressed A549 tumor growth in nude mice. Our findings suggest that econazole is a new PI3K inhibitor and a potential drug that can be used in lung cancer treatment alone or in combination with cisplatin. Nature Publishing Group UK 2017-12-21 /pmc/articles/PMC5740072/ /pubmed/29269744 http://dx.doi.org/10.1038/s41598-017-18178-0 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Dong, Chao
Yang, Runxiang
Li, Hongjian
Ke, Kunbin
Luo, Chunxiang
Yang, Fang
Shi, Xi-Nan
Zhu, Ying
Liu, Xu
Wong, Man-Hon
Lin, Guimiao
Wang, Xiaomei
Leung, Kwong-Sak
Kung, Hsiang-Fu
Chen, Ceshi
Lin, Marie Chia-mi
Econazole nitrate inhibits PI3K activity and promotes apoptosis in lung cancer cells
title Econazole nitrate inhibits PI3K activity and promotes apoptosis in lung cancer cells
title_full Econazole nitrate inhibits PI3K activity and promotes apoptosis in lung cancer cells
title_fullStr Econazole nitrate inhibits PI3K activity and promotes apoptosis in lung cancer cells
title_full_unstemmed Econazole nitrate inhibits PI3K activity and promotes apoptosis in lung cancer cells
title_short Econazole nitrate inhibits PI3K activity and promotes apoptosis in lung cancer cells
title_sort econazole nitrate inhibits pi3k activity and promotes apoptosis in lung cancer cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5740072/
https://www.ncbi.nlm.nih.gov/pubmed/29269744
http://dx.doi.org/10.1038/s41598-017-18178-0
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