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Ethacrynic acid improves the antitumor effects of irreversible epidermal growth factor receptor tyrosine kinase inhibitors in breast cancer

Prolonged treatment of breast cancer with epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) often results in acquired resistance and a narrow therapeutic index. One strategy to improve the therapeutic effects of EGFR TKIs is to combine them with drugs used for other clinical...

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Autores principales: Liu, Bing, Huang, XinPing, Hu, YunLong, Chen, TingTing, Peng, BoYa, Gao, NingNing, Jin, ZhenChao, Jia, TieLiu, Zhang, Na, Wang, ZhuLin, Jin, GuangYi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5295410/
https://www.ncbi.nlm.nih.gov/pubmed/27487128
http://dx.doi.org/10.18632/oncotarget.10846
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author Liu, Bing
Huang, XinPing
Hu, YunLong
Chen, TingTing
Peng, BoYa
Gao, NingNing
Jin, ZhenChao
Jia, TieLiu
Zhang, Na
Wang, ZhuLin
Jin, GuangYi
author_facet Liu, Bing
Huang, XinPing
Hu, YunLong
Chen, TingTing
Peng, BoYa
Gao, NingNing
Jin, ZhenChao
Jia, TieLiu
Zhang, Na
Wang, ZhuLin
Jin, GuangYi
author_sort Liu, Bing
collection PubMed
description Prolonged treatment of breast cancer with epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) often results in acquired resistance and a narrow therapeutic index. One strategy to improve the therapeutic effects of EGFR TKIs is to combine them with drugs used for other clinical indications. Ethacrynic acid (EA) is an FDA approved drug that may have antitumor effects and may enhance the cytotoxicity of chemotherapeutic agents by binding to glutathione and inhibiting WNT signaling. While the α,β-unsaturated-keto structure of EA is similar to that of irreversible TKIs, the mechanism of action of EA when combined with irreversible EGFR TKIs in breast cancer remains unknown. We therefore investigated the combination of irreversible EGFR TKIs and EA. We found that irreversible EGFR TKIs and EA synergistically inhibit breast cancer both in vitro and in vivo. The combination of EGFR TKIs and EA induces necrosis and cell cycle arrest and represses WNT/β-catenin signaling as well as MAPK-ERK1/2 signaling. We conclude that EA synergistically enhances the antitumor effects of irreversible EGFR TKIs in breast cancer.
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spelling pubmed-52954102017-02-08 Ethacrynic acid improves the antitumor effects of irreversible epidermal growth factor receptor tyrosine kinase inhibitors in breast cancer Liu, Bing Huang, XinPing Hu, YunLong Chen, TingTing Peng, BoYa Gao, NingNing Jin, ZhenChao Jia, TieLiu Zhang, Na Wang, ZhuLin Jin, GuangYi Oncotarget Research Paper Prolonged treatment of breast cancer with epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) often results in acquired resistance and a narrow therapeutic index. One strategy to improve the therapeutic effects of EGFR TKIs is to combine them with drugs used for other clinical indications. Ethacrynic acid (EA) is an FDA approved drug that may have antitumor effects and may enhance the cytotoxicity of chemotherapeutic agents by binding to glutathione and inhibiting WNT signaling. While the α,β-unsaturated-keto structure of EA is similar to that of irreversible TKIs, the mechanism of action of EA when combined with irreversible EGFR TKIs in breast cancer remains unknown. We therefore investigated the combination of irreversible EGFR TKIs and EA. We found that irreversible EGFR TKIs and EA synergistically inhibit breast cancer both in vitro and in vivo. The combination of EGFR TKIs and EA induces necrosis and cell cycle arrest and represses WNT/β-catenin signaling as well as MAPK-ERK1/2 signaling. We conclude that EA synergistically enhances the antitumor effects of irreversible EGFR TKIs in breast cancer. Impact Journals LLC 2016-07-26 /pmc/articles/PMC5295410/ /pubmed/27487128 http://dx.doi.org/10.18632/oncotarget.10846 Text en Copyright: © 2016 Liu et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Liu, Bing
Huang, XinPing
Hu, YunLong
Chen, TingTing
Peng, BoYa
Gao, NingNing
Jin, ZhenChao
Jia, TieLiu
Zhang, Na
Wang, ZhuLin
Jin, GuangYi
Ethacrynic acid improves the antitumor effects of irreversible epidermal growth factor receptor tyrosine kinase inhibitors in breast cancer
title Ethacrynic acid improves the antitumor effects of irreversible epidermal growth factor receptor tyrosine kinase inhibitors in breast cancer
title_full Ethacrynic acid improves the antitumor effects of irreversible epidermal growth factor receptor tyrosine kinase inhibitors in breast cancer
title_fullStr Ethacrynic acid improves the antitumor effects of irreversible epidermal growth factor receptor tyrosine kinase inhibitors in breast cancer
title_full_unstemmed Ethacrynic acid improves the antitumor effects of irreversible epidermal growth factor receptor tyrosine kinase inhibitors in breast cancer
title_short Ethacrynic acid improves the antitumor effects of irreversible epidermal growth factor receptor tyrosine kinase inhibitors in breast cancer
title_sort ethacrynic acid improves the antitumor effects of irreversible epidermal growth factor receptor tyrosine kinase inhibitors in breast cancer
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5295410/
https://www.ncbi.nlm.nih.gov/pubmed/27487128
http://dx.doi.org/10.18632/oncotarget.10846
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