Research Progress of Acquired Resistance Mediated by MET Amplification 
in Advanced Non-small Cell Lung Cancer

Mesenchymal-epithelial transition factor (MET) amplification is an important driver of resistance in epidermal growth factor receptor (EGFR)-mutant non-small cell lung cancer (NSCLC), and the combination of MET proto-oncogene (MET) and EGFR-tyrosine kinase inhibitors (TKIs) has shown promise in over...

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Main Authors: Sisi PAN, Na WANG, Xia SONG
Format: Article
Language:zho
Published: Chinese Anti-Cancer Association; Chinese Antituberculosis Association 2022-08-01
Series:Chinese Journal of Lung Cancer
Subjects:
Online Access:http://dx.doi.org/10.3779/j.issn.1009-3419.2022.102.23
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author Sisi PAN
Na WANG
Xia SONG
author_facet Sisi PAN
Na WANG
Xia SONG
author_sort Sisi PAN
collection DOAJ
description Mesenchymal-epithelial transition factor (MET) amplification is an important driver of resistance in epidermal growth factor receptor (EGFR)-mutant non-small cell lung cancer (NSCLC), and the combination of MET proto-oncogene (MET) and EGFR-tyrosine kinase inhibitors (TKIs) has shown promise in overcoming this molecularly defined acquired resistance. Emerging data also demonstrate MET amplification as a resistance driver to TKIs-treated anaplastic lymphoma kinase (ALK)-, RET-, and ROS1-fusion NSCLC. Here, we review the literature on recent research progress of MET amplification as a resistance driver to targeted therapy in oncogene-driven NSCLC and summarize the progress of clinical strategies to overcome the resistance mechanism.
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spelling doaj.art-fef825899f304a7ab658c7db0724bbe92022-12-22T04:02:38ZzhoChinese Anti-Cancer Association; Chinese Antituberculosis AssociationChinese Journal of Lung Cancer1009-34191999-61872022-08-0125861562110.3779/j.issn.1009-3419.2022.102.23Research Progress of Acquired Resistance Mediated by MET Amplification 
in Advanced Non-small Cell Lung CancerSisi PAN0Na WANG1Xia SONG2The Second Clinical Medical College of Shanxi Medical University, Taiyuan 030001, ChinaThe Second Clinical Medical College of Shanxi Medical University, Taiyuan 030001, ChinaThe Second Department of Respiratory, Shanxi Provincial Cancer Hospital, Taiyuan 030013, ChinaMesenchymal-epithelial transition factor (MET) amplification is an important driver of resistance in epidermal growth factor receptor (EGFR)-mutant non-small cell lung cancer (NSCLC), and the combination of MET proto-oncogene (MET) and EGFR-tyrosine kinase inhibitors (TKIs) has shown promise in overcoming this molecularly defined acquired resistance. Emerging data also demonstrate MET amplification as a resistance driver to TKIs-treated anaplastic lymphoma kinase (ALK)-, RET-, and ROS1-fusion NSCLC. Here, we review the literature on recent research progress of MET amplification as a resistance driver to targeted therapy in oncogene-driven NSCLC and summarize the progress of clinical strategies to overcome the resistance mechanism.http://dx.doi.org/10.3779/j.issn.1009-3419.2022.102.23lung neoplasmstargeted therapymet amplificationacquired resistance
spellingShingle Sisi PAN
Na WANG
Xia SONG
Research Progress of Acquired Resistance Mediated by MET Amplification 
in Advanced Non-small Cell Lung Cancer
Chinese Journal of Lung Cancer
lung neoplasms
targeted therapy
met amplification
acquired resistance
title Research Progress of Acquired Resistance Mediated by MET Amplification 
in Advanced Non-small Cell Lung Cancer
title_full Research Progress of Acquired Resistance Mediated by MET Amplification 
in Advanced Non-small Cell Lung Cancer
title_fullStr Research Progress of Acquired Resistance Mediated by MET Amplification 
in Advanced Non-small Cell Lung Cancer
title_full_unstemmed Research Progress of Acquired Resistance Mediated by MET Amplification 
in Advanced Non-small Cell Lung Cancer
title_short Research Progress of Acquired Resistance Mediated by MET Amplification 
in Advanced Non-small Cell Lung Cancer
title_sort research progress of acquired resistance mediated by met amplification 
in advanced non small cell lung cancer
topic lung neoplasms
targeted therapy
met amplification
acquired resistance
url http://dx.doi.org/10.3779/j.issn.1009-3419.2022.102.23
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