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Establishing Dual Resistance to EGFR-TKI and MET-TKI in Lung Adenocarcinoma Cells In Vitro with a 2-step Dose-escalation Procedure
Published on: August 11, 2017
PAI-1 mediates acquired resistance to MET-targeted therapy in non-small cell lung cancer
Yin Min Thu1, Ken Suzawa1, Shuta Tomida2
1Department of General Thoracic Surgery and Breast and Endocrinological Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
Abstract:
Mechanisms underlying primary and acquired resistance to MET tyrosine kinase inhibitors (TKIs) in managing non-small cell lung cancer remain unclear. In this study, we investigated the possible mechanisms acquired for crizotinib in MET-amplified lung carcinoma cell lines. Two MET-amplified lung cancer cell lines, EBC-1 and H1993, were established for acquired resistance to MET-TKI crizotinib and were functionally elucidated. Genomic and transcriptomic data were used to assess the factors contributing to the resistance mechanism, and the alterations hypothesized to confer resistance were validated. Multiple mechanisms underlie acquired resistance to crizotinib in MET-amplified lung cancer cell lines. In EBC-1-derived resistant cells, the overexpression of SERPINE1, the gene encoding plasminogen activator inhibitor-1 (PAI-1), mediated the drug resistance mechanism. Crizotinib resistance was addressed by combination therapy with a PAI-1 inhibitor and PAI-1 knockdown. Another mechanism of resistance in different subline cells of EBC-1 was evaluated as epithelial-to-mesenchymal transition with the upregulation of antiapoptotic proteins. In H1993-derived resistant cells, MEK inhibitors could be a potential therapeutic strategy for overcoming resistance with downstream mitogen-activated protein kinase pathway activation. In this study, we revealed the different mechanisms of acquired resistance to the MET inhibitor crizotinib with potential therapeutic application in patients with MET-amplified lung carcinoma.
Insights
Acquired resistance to crizotinib in MET-amplified lung cancer involves multiple mechanisms, including SERPINE1 overexpression and epithelial-to-mesenchymal transition. Targeting these pathways offers potential therapeutic strategies for non-small cell lung cancer.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Mechanisms of resistance to MET tyrosine kinase inhibitors (TKIs) in non-small cell lung cancer (NSCLC) are not fully understood.
- MET amplification is a driver mutation in a subset of NSCLC, making MET TKIs a target for therapy.
Purpose of the Study:
- To investigate acquired resistance mechanisms to the MET TKI crizotinib in MET-amplified NSCLC cell lines.
- To identify potential therapeutic strategies to overcome crizotinib resistance.
Main Methods:
- Established crizotinib-resistant cell lines (EBC-1 and H1993) from MET-amplified NSCLC.
- Utilized genomic and transcriptomic analyses to identify resistance factors.
- Validated hypothesized resistance alterations and tested combination therapies.
Main Results:
- In EBC-1 derived cells, SERPINE1 (PAI-1) overexpression was a key resistance mechanism, responsive to PAI-1 inhibition and knockdown.
- Another EBC-1 subline exhibited resistance via epithelial-to-mesenchymal transition with upregulated antiapoptotic proteins.
- H1993 derived cells showed resistance linked to downstream mitogen-activated protein kinase pathway activation, suggesting MEK inhibitors as a therapeutic option.
Conclusions:
- Acquired resistance to crizotinib in MET-amplified NSCLC is multifactorial.
- SERPINE1 inhibition and MEK inhibition represent promising strategies to overcome crizotinib resistance in specific resistant NSCLC contexts.
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