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AZD0530 sensitizes drug‐resistant ALK‐positive lung cancer cells by inhibiting SRC signaling

Most tumors develop resistance to targeted cancer drugs, even though these drugs have produced substantial clinical responses. Here we established anaplastic lymphoma kinase (ALK)‐positive drug‐resistant lung cancer cell lines, which are resistant to ceritinib (LDK378). We found that ceritinib treat...

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Detalles Bibliográficos
Autores principales: Zhao, Yi, Yang, Yi, Xu, Yunhua, Lu, Shun, Jian, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5377386/
https://www.ncbi.nlm.nih.gov/pubmed/28396832
http://dx.doi.org/10.1002/2211-5463.12162
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author Zhao, Yi
Yang, Yi
Xu, Yunhua
Lu, Shun
Jian, Hong
author_facet Zhao, Yi
Yang, Yi
Xu, Yunhua
Lu, Shun
Jian, Hong
author_sort Zhao, Yi
collection PubMed
description Most tumors develop resistance to targeted cancer drugs, even though these drugs have produced substantial clinical responses. Here we established anaplastic lymphoma kinase (ALK)‐positive drug‐resistant lung cancer cell lines, which are resistant to ceritinib (LDK378). We found that ceritinib treatment resulted in robust upregulation of SRC activity, as measured by the phosphorylation of the SRC substrate paxillin. Knockdown of SRC alone with siRNA effectively sensitized ceritinib resistance in ALK‐positive cells. Furthermore, SRC inhibition by AZD0530 was effective in ALK‐resistant cancer cells. Thus, ALK inhibition by ceritinib may lead to upregulation of SRC signaling, and AZD0530 could serve as a potential drug in the clinic to treat ALK‐resistant lung cancer patients.
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spelling pubmed-53773862017-04-10 AZD0530 sensitizes drug‐resistant ALK‐positive lung cancer cells by inhibiting SRC signaling Zhao, Yi Yang, Yi Xu, Yunhua Lu, Shun Jian, Hong FEBS Open Bio Research Articles Most tumors develop resistance to targeted cancer drugs, even though these drugs have produced substantial clinical responses. Here we established anaplastic lymphoma kinase (ALK)‐positive drug‐resistant lung cancer cell lines, which are resistant to ceritinib (LDK378). We found that ceritinib treatment resulted in robust upregulation of SRC activity, as measured by the phosphorylation of the SRC substrate paxillin. Knockdown of SRC alone with siRNA effectively sensitized ceritinib resistance in ALK‐positive cells. Furthermore, SRC inhibition by AZD0530 was effective in ALK‐resistant cancer cells. Thus, ALK inhibition by ceritinib may lead to upregulation of SRC signaling, and AZD0530 could serve as a potential drug in the clinic to treat ALK‐resistant lung cancer patients. John Wiley and Sons Inc. 2017-03-10 /pmc/articles/PMC5377386/ /pubmed/28396832 http://dx.doi.org/10.1002/2211-5463.12162 Text en © 2016 The Authors. Published by FEBS Press and John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Zhao, Yi
Yang, Yi
Xu, Yunhua
Lu, Shun
Jian, Hong
AZD0530 sensitizes drug‐resistant ALK‐positive lung cancer cells by inhibiting SRC signaling
title AZD0530 sensitizes drug‐resistant ALK‐positive lung cancer cells by inhibiting SRC signaling
title_full AZD0530 sensitizes drug‐resistant ALK‐positive lung cancer cells by inhibiting SRC signaling
title_fullStr AZD0530 sensitizes drug‐resistant ALK‐positive lung cancer cells by inhibiting SRC signaling
title_full_unstemmed AZD0530 sensitizes drug‐resistant ALK‐positive lung cancer cells by inhibiting SRC signaling
title_short AZD0530 sensitizes drug‐resistant ALK‐positive lung cancer cells by inhibiting SRC signaling
title_sort azd0530 sensitizes drug‐resistant alk‐positive lung cancer cells by inhibiting src signaling
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5377386/
https://www.ncbi.nlm.nih.gov/pubmed/28396832
http://dx.doi.org/10.1002/2211-5463.12162
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