Cargando…

Cell Line Models for Acquired Resistance to First-Line Osimertinib in Lung Cancers—Applications and Limitations

Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) are first-line drugs for lung cancers with activating EGFR mutations. Although first- and second-generation EGFR-TKIs were standard first-line treatments, acquired resistance (AR) to these drugs is almost inevitable. Cell line...

Descripción completa

Detalles Bibliográficos
Autores principales: Ohara, Shuta, Suda, Kenichi, Mitsudomi, Tetsuya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7915563/
https://www.ncbi.nlm.nih.gov/pubmed/33572269
http://dx.doi.org/10.3390/cells10020354
_version_ 1783657272318099456
author Ohara, Shuta
Suda, Kenichi
Mitsudomi, Tetsuya
author_facet Ohara, Shuta
Suda, Kenichi
Mitsudomi, Tetsuya
author_sort Ohara, Shuta
collection PubMed
description Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) are first-line drugs for lung cancers with activating EGFR mutations. Although first- and second-generation EGFR-TKIs were standard first-line treatments, acquired resistance (AR) to these drugs is almost inevitable. Cell line models have been widely used to explore the molecular mechanisms of AR to first- and second-generation EGFR-TKIs. Many research groups, including ours, have established AR cell lines that harbor the EGFR T790M secondary mutation, MET gene amplification, or epithelial–mesenchymal transition (EMT) features, which are all found in clinical specimens obtained from TKI-refractory lesions. Currently, many oncologists prescribe osimertinib, a third-generation EGFR-TKI that can overcome T790M-mediated resistance, as a first-line TKI. Although few clinical data are available about AR mechanisms that arise when osimertinib is used as a first-line therapy, many research groups have established cell lines with AR to osimertinib and have reported on their AR mechanisms. In this review, we summarize the findings on AR mechanisms against first-line osimertinib obtained from analyses of cell line models.
format Online
Article
Text
id pubmed-7915563
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-79155632021-03-01 Cell Line Models for Acquired Resistance to First-Line Osimertinib in Lung Cancers—Applications and Limitations Ohara, Shuta Suda, Kenichi Mitsudomi, Tetsuya Cells Review Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) are first-line drugs for lung cancers with activating EGFR mutations. Although first- and second-generation EGFR-TKIs were standard first-line treatments, acquired resistance (AR) to these drugs is almost inevitable. Cell line models have been widely used to explore the molecular mechanisms of AR to first- and second-generation EGFR-TKIs. Many research groups, including ours, have established AR cell lines that harbor the EGFR T790M secondary mutation, MET gene amplification, or epithelial–mesenchymal transition (EMT) features, which are all found in clinical specimens obtained from TKI-refractory lesions. Currently, many oncologists prescribe osimertinib, a third-generation EGFR-TKI that can overcome T790M-mediated resistance, as a first-line TKI. Although few clinical data are available about AR mechanisms that arise when osimertinib is used as a first-line therapy, many research groups have established cell lines with AR to osimertinib and have reported on their AR mechanisms. In this review, we summarize the findings on AR mechanisms against first-line osimertinib obtained from analyses of cell line models. MDPI 2021-02-09 /pmc/articles/PMC7915563/ /pubmed/33572269 http://dx.doi.org/10.3390/cells10020354 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Ohara, Shuta
Suda, Kenichi
Mitsudomi, Tetsuya
Cell Line Models for Acquired Resistance to First-Line Osimertinib in Lung Cancers—Applications and Limitations
title Cell Line Models for Acquired Resistance to First-Line Osimertinib in Lung Cancers—Applications and Limitations
title_full Cell Line Models for Acquired Resistance to First-Line Osimertinib in Lung Cancers—Applications and Limitations
title_fullStr Cell Line Models for Acquired Resistance to First-Line Osimertinib in Lung Cancers—Applications and Limitations
title_full_unstemmed Cell Line Models for Acquired Resistance to First-Line Osimertinib in Lung Cancers—Applications and Limitations
title_short Cell Line Models for Acquired Resistance to First-Line Osimertinib in Lung Cancers—Applications and Limitations
title_sort cell line models for acquired resistance to first-line osimertinib in lung cancers—applications and limitations
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7915563/
https://www.ncbi.nlm.nih.gov/pubmed/33572269
http://dx.doi.org/10.3390/cells10020354
work_keys_str_mv AT oharashuta celllinemodelsforacquiredresistancetofirstlineosimertinibinlungcancersapplicationsandlimitations
AT sudakenichi celllinemodelsforacquiredresistancetofirstlineosimertinibinlungcancersapplicationsandlimitations
AT mitsudomitetsuya celllinemodelsforacquiredresistancetofirstlineosimertinibinlungcancersapplicationsandlimitations