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Amplification of EGFR T790M causes resistance to an irreversible EGFR inhibitor
Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors, gefitinib and erlotinib, are effective therapies against mutant non-small cell lung cancers (NSCLCs). Treatment is limited by the development of resistance in part explained by the gain of a secondary EGFR mutation, T790M, at the ga...
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| Autori principali: | , , , , , , , , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2010
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2859699/ https://ncbi.nlm.nih.gov/pubmed/20118985 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/onc.2009.526 |
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