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Oncotarget. 2014 Sep 15;5(17):7328-41.

Overcoming EMT-associated resistance to anti-cancer drugs via Src/FAK pathway inhibition.

Author information

1
Department of Discovery Oncology, Genentech, 1 DNA Way, South San Francisco, CA.
2
Department of Discovery Protein Chemistry, Genentech, 1 DNA Way, South San Francisco, CA.
3
Department of Discovery Nonclinical Biostatistics, Genentech, 1 DNA Way, South San Francisco, CA.

Abstract

Epithelial to mesenchymal transition (EMT) is a key process in embryonic development and has been associated with cancer metastasis and drug resistance. For example, in EGFR mutated non-small cell lung cancers (NSCLC), EMT has been associated with acquired resistance to the EGFR inhibitor erlotinib. Moreover, "EGFR-addicted" cancer cell lines induced to undergo EMT become erlotinib-resistant in vitro. To identify potential therapeutic vulnerabilities specifically within these mesenchymal, erlotinib-resistant cells, we performed a small molecule screen of ~200 established anti-cancer agents using the EGFR mutant NSCLC HCC827 cell line and a corresponding mesenchymal derivative line. The mesenchymal cells were more resistant to most tested agents; however, a small number of agents showed selective growth inhibitory activity against the mesenchymal cells, with the most potent being the Abl/Src inhibitor, dasatinib. Analysis of the tyrosine phospho-proteome revealed several Src/FAK pathway kinases that were differentially phosphorylated in the mesenchymal cells, and RNAi depletion of the core Src/FAK pathway components in these mesenchymal cells caused apoptosis. These findings reveal a novel role for Src/FAK pathway kinases in drug resistance and identify dasatinib as a potential therapeutic for treatment of erlotinib resistance associated with EMT.

PMID:
25193862
PMCID:
PMC4202126
DOI:
10.18632/oncotarget.2397
[Indexed for MEDLINE]
Free PMC Article

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