Effect of dasatinib on EMT-mediated-mechanism of resistance against EGFR inhibitors in lung cancer cells
Highlights • A Combination of erlotinib and dasatinib prevented the acquired resistance via EMT. • The acquired resistance mechanism of the combination therapy was T790 M mutation. • Preemptive combination therapy may be a promising strategy.
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Veröffentlicht in: | Lung cancer (Amsterdam, Netherlands) Netherlands), 2017-02, Vol.104, p.85-90 |
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container_title | Lung cancer (Amsterdam, Netherlands) |
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creator | Sesumi, Yuichi Suda, Kenichi Mizuuchi, Hiroshi Kobayashi, Yoshihisa Sato, Katsuaki Chiba, Masato Masaki, Shimoji Tomizawa, Kenji Takemoto, Toshiki Mitsudomi, Tetsuya |
description | Highlights • A Combination of erlotinib and dasatinib prevented the acquired resistance via EMT. • The acquired resistance mechanism of the combination therapy was T790 M mutation. • Preemptive combination therapy may be a promising strategy. |
doi_str_mv | 10.1016/j.lungcan.2016.12.012 |
format | Article |
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Suda, Kenichi ; Mizuuchi, Hiroshi ; Kobayashi, Yoshihisa ; Sato, Katsuaki ; Chiba, Masato ; Masaki, Shimoji ; Tomizawa, Kenji ; Takemoto, Toshiki ; Mitsudomi, Tetsuya</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c570t-3e91097f96b6e3030865a0e87f120bf4500678d6e7286bf66db0015abb2bca9e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Acquired resistance</topic><topic>Carcinoma, Non-Small-Cell Lung - drug therapy</topic><topic>Carcinoma, Non-Small-Cell Lung - genetics</topic><topic>Carcinoma, Non-Small-Cell Lung - pathology</topic><topic>Cell Line, Tumor - drug effects</topic><topic>Cell Line, Tumor - metabolism</topic><topic>Dasatinib</topic><topic>Dasatinib - pharmacology</topic><topic>Drug Resistance, Neoplasm</topic><topic>Drug Therapy, Combination - methods</topic><topic>Epithelial-mesenchymal transition</topic><topic>Epithelial-Mesenchymal Transition - drug effects</topic><topic>Epithelial-Mesenchymal Transition - genetics</topic><topic>Erlotinib Hydrochloride</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>Humans</topic><topic>Lung Neoplasms - drug therapy</topic><topic>Lung Neoplasms - genetics</topic><topic>Lung Neoplasms - pathology</topic><topic>Mutation</topic><topic>Non-small cell lung cancer</topic><topic>Protein Kinase Inhibitors - pharmacology</topic><topic>Pulmonary/Respiratory</topic><topic>Receptor, Epidermal Growth Factor - antagonists & inhibitors</topic><topic>Receptor, Epidermal Growth Factor - genetics</topic><topic>Third- generation EGFR-TKI</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sesumi, Yuichi</creatorcontrib><creatorcontrib>Suda, Kenichi</creatorcontrib><creatorcontrib>Mizuuchi, Hiroshi</creatorcontrib><creatorcontrib>Kobayashi, Yoshihisa</creatorcontrib><creatorcontrib>Sato, Katsuaki</creatorcontrib><creatorcontrib>Chiba, Masato</creatorcontrib><creatorcontrib>Masaki, Shimoji</creatorcontrib><creatorcontrib>Tomizawa, Kenji</creatorcontrib><creatorcontrib>Takemoto, Toshiki</creatorcontrib><creatorcontrib>Mitsudomi, Tetsuya</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Lung cancer (Amsterdam, Netherlands)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sesumi, Yuichi</au><au>Suda, Kenichi</au><au>Mizuuchi, Hiroshi</au><au>Kobayashi, Yoshihisa</au><au>Sato, Katsuaki</au><au>Chiba, Masato</au><au>Masaki, Shimoji</au><au>Tomizawa, Kenji</au><au>Takemoto, Toshiki</au><au>Mitsudomi, Tetsuya</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of dasatinib on EMT-mediated-mechanism of resistance against EGFR inhibitors in lung cancer cells</atitle><jtitle>Lung cancer (Amsterdam, Netherlands)</jtitle><addtitle>Lung Cancer</addtitle><date>2017-02-01</date><risdate>2017</risdate><volume>104</volume><spage>85</spage><epage>90</epage><pages>85-90</pages><issn>0169-5002</issn><eissn>1872-8332</eissn><abstract>Highlights • A Combination of erlotinib and dasatinib prevented the acquired resistance via EMT. • The acquired resistance mechanism of the combination therapy was T790 M mutation. • Preemptive combination therapy may be a promising strategy.</abstract><cop>Ireland</cop><pub>Elsevier B.V</pub><pmid>28213007</pmid><doi>10.1016/j.lungcan.2016.12.012</doi><tpages>6</tpages></addata></record> |
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subjects | Acquired resistance Carcinoma, Non-Small-Cell Lung - drug therapy Carcinoma, Non-Small-Cell Lung - genetics Carcinoma, Non-Small-Cell Lung - pathology Cell Line, Tumor - drug effects Cell Line, Tumor - metabolism Dasatinib Dasatinib - pharmacology Drug Resistance, Neoplasm Drug Therapy, Combination - methods Epithelial-mesenchymal transition Epithelial-Mesenchymal Transition - drug effects Epithelial-Mesenchymal Transition - genetics Erlotinib Hydrochloride Hematology, Oncology and Palliative Medicine Humans Lung Neoplasms - drug therapy Lung Neoplasms - genetics Lung Neoplasms - pathology Mutation Non-small cell lung cancer Protein Kinase Inhibitors - pharmacology Pulmonary/Respiratory Receptor, Epidermal Growth Factor - antagonists & inhibitors Receptor, Epidermal Growth Factor - genetics Third- generation EGFR-TKI Treatment Outcome |
title | Effect of dasatinib on EMT-mediated-mechanism of resistance against EGFR inhibitors in lung cancer cells |
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