Cargando…

Characterization of epithelial-mesenchymal transition intermediate/hybrid phenotypes associated to resistance to EGFR inhibitors in non-small cell lung cancer cell lines

Increasing evidence points to a key role played by epithelial-mesenchymal transition (EMT) in cancer progression and drug resistance. In this study, we used wet and in silico approaches to investigate whether EMT phenotypes are associated to resistance to target therapy in a non-small cell lung canc...

Descripción completa

Detalles Bibliográficos
Autores principales: Fustaino, Valentina, Presutti, Dario, Colombo, Teresa, Cardinali, Beatrice, Papoff, Giuliana, Brandi, Rossella, Bertolazzi, Paola, Felici, Giovanni, Ruberti, Giovina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5732732/
https://www.ncbi.nlm.nih.gov/pubmed/29262566
http://dx.doi.org/10.18632/oncotarget.21132
_version_ 1783286767116353536
author Fustaino, Valentina
Presutti, Dario
Colombo, Teresa
Cardinali, Beatrice
Papoff, Giuliana
Brandi, Rossella
Bertolazzi, Paola
Felici, Giovanni
Ruberti, Giovina
author_facet Fustaino, Valentina
Presutti, Dario
Colombo, Teresa
Cardinali, Beatrice
Papoff, Giuliana
Brandi, Rossella
Bertolazzi, Paola
Felici, Giovanni
Ruberti, Giovina
author_sort Fustaino, Valentina
collection PubMed
description Increasing evidence points to a key role played by epithelial-mesenchymal transition (EMT) in cancer progression and drug resistance. In this study, we used wet and in silico approaches to investigate whether EMT phenotypes are associated to resistance to target therapy in a non-small cell lung cancer model system harboring activating mutations of the epidermal growth factor receptor. The combination of different analysis techniques allowed us to describe intermediate/hybrid and complete EMT phenotypes respectively in HCC827- and HCC4006-derived drug-resistant human cancer cell lines. Interestingly, intermediate/hybrid EMT phenotypes, a collective cell migration and increased stem-like ability associate to resistance to the epidermal growth factor receptor inhibitor, erlotinib, in HCC827 derived cell lines. Moreover, the use of three complementary approaches for gene expression analysis supported the identification of a small EMT-related gene list, which may have otherwise been overlooked by standard stand-alone methods for gene expression analysis.
format Online
Article
Text
id pubmed-5732732
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Impact Journals LLC
record_format MEDLINE/PubMed
spelling pubmed-57327322017-12-19 Characterization of epithelial-mesenchymal transition intermediate/hybrid phenotypes associated to resistance to EGFR inhibitors in non-small cell lung cancer cell lines Fustaino, Valentina Presutti, Dario Colombo, Teresa Cardinali, Beatrice Papoff, Giuliana Brandi, Rossella Bertolazzi, Paola Felici, Giovanni Ruberti, Giovina Oncotarget Research Paper Increasing evidence points to a key role played by epithelial-mesenchymal transition (EMT) in cancer progression and drug resistance. In this study, we used wet and in silico approaches to investigate whether EMT phenotypes are associated to resistance to target therapy in a non-small cell lung cancer model system harboring activating mutations of the epidermal growth factor receptor. The combination of different analysis techniques allowed us to describe intermediate/hybrid and complete EMT phenotypes respectively in HCC827- and HCC4006-derived drug-resistant human cancer cell lines. Interestingly, intermediate/hybrid EMT phenotypes, a collective cell migration and increased stem-like ability associate to resistance to the epidermal growth factor receptor inhibitor, erlotinib, in HCC827 derived cell lines. Moreover, the use of three complementary approaches for gene expression analysis supported the identification of a small EMT-related gene list, which may have otherwise been overlooked by standard stand-alone methods for gene expression analysis. Impact Journals LLC 2017-09-22 /pmc/articles/PMC5732732/ /pubmed/29262566 http://dx.doi.org/10.18632/oncotarget.21132 Text en Copyright: © 2017 Fustaino et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Fustaino, Valentina
Presutti, Dario
Colombo, Teresa
Cardinali, Beatrice
Papoff, Giuliana
Brandi, Rossella
Bertolazzi, Paola
Felici, Giovanni
Ruberti, Giovina
Characterization of epithelial-mesenchymal transition intermediate/hybrid phenotypes associated to resistance to EGFR inhibitors in non-small cell lung cancer cell lines
title Characterization of epithelial-mesenchymal transition intermediate/hybrid phenotypes associated to resistance to EGFR inhibitors in non-small cell lung cancer cell lines
title_full Characterization of epithelial-mesenchymal transition intermediate/hybrid phenotypes associated to resistance to EGFR inhibitors in non-small cell lung cancer cell lines
title_fullStr Characterization of epithelial-mesenchymal transition intermediate/hybrid phenotypes associated to resistance to EGFR inhibitors in non-small cell lung cancer cell lines
title_full_unstemmed Characterization of epithelial-mesenchymal transition intermediate/hybrid phenotypes associated to resistance to EGFR inhibitors in non-small cell lung cancer cell lines
title_short Characterization of epithelial-mesenchymal transition intermediate/hybrid phenotypes associated to resistance to EGFR inhibitors in non-small cell lung cancer cell lines
title_sort characterization of epithelial-mesenchymal transition intermediate/hybrid phenotypes associated to resistance to egfr inhibitors in non-small cell lung cancer cell lines
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5732732/
https://www.ncbi.nlm.nih.gov/pubmed/29262566
http://dx.doi.org/10.18632/oncotarget.21132
work_keys_str_mv AT fustainovalentina characterizationofepithelialmesenchymaltransitionintermediatehybridphenotypesassociatedtoresistancetoegfrinhibitorsinnonsmallcelllungcancercelllines
AT presuttidario characterizationofepithelialmesenchymaltransitionintermediatehybridphenotypesassociatedtoresistancetoegfrinhibitorsinnonsmallcelllungcancercelllines
AT colomboteresa characterizationofepithelialmesenchymaltransitionintermediatehybridphenotypesassociatedtoresistancetoegfrinhibitorsinnonsmallcelllungcancercelllines
AT cardinalibeatrice characterizationofepithelialmesenchymaltransitionintermediatehybridphenotypesassociatedtoresistancetoegfrinhibitorsinnonsmallcelllungcancercelllines
AT papoffgiuliana characterizationofepithelialmesenchymaltransitionintermediatehybridphenotypesassociatedtoresistancetoegfrinhibitorsinnonsmallcelllungcancercelllines
AT brandirossella characterizationofepithelialmesenchymaltransitionintermediatehybridphenotypesassociatedtoresistancetoegfrinhibitorsinnonsmallcelllungcancercelllines
AT bertolazzipaola characterizationofepithelialmesenchymaltransitionintermediatehybridphenotypesassociatedtoresistancetoegfrinhibitorsinnonsmallcelllungcancercelllines
AT felicigiovanni characterizationofepithelialmesenchymaltransitionintermediatehybridphenotypesassociatedtoresistancetoegfrinhibitorsinnonsmallcelllungcancercelllines
AT rubertigiovina characterizationofepithelialmesenchymaltransitionintermediatehybridphenotypesassociatedtoresistancetoegfrinhibitorsinnonsmallcelllungcancercelllines