Src mediates cigarette smoke-induced resistance to tyrosine kinase inhibitors in NSCLC cells

Simone Filosto, David S. Baston, Samuel Chung, Cathleen R. Becker, Tzipora Goldkorn

Research output: Contribution to journalArticlepeer-review

28 Scopus citations

Abstract

The EGF receptor (EGFR) is a proto-oncogene commonly dysregulated in several cancers including non- small cell lung carcinoma (NSCLC) and, thus, is targeted for treatment using tyrosine kinase inhibitors (TKI) such as erlotinib. However, despite the efficacy observed in patients withNSCLCharboring oncogenic variants of the EGFR, general ineffectiveness of TKIs in patients with NSCLC who are current and former smokers necessitates identification of novel mechanisms to overcome this phenomenon. Previously, we showed that NSCLC cells harboring either wild-type (WT) EGFR or oncogenic mutant (MT) L858R EGFR become resistant to the effects of TKIs when exposed to cigarette smoke, evidenced by their autophosphorylation and prolonged downstream signaling. Here, we present Src as a target mediating cigarette smoke-induced resistance to TKIs in bothWTEGFR- and L858RMTEGFR-expressing NSCLCcells. First, weshow that cigarette smoke exposure of A549 cells leads to time-dependent activation of Src, which then abnormally binds to the WT EGFR causing TKI resistance, contrasting previous observations of constitutive binding between inactive Src and TKIsensitive L858R MT EGFR. Next, we show that Src inhibition restores TKI sensitivity in cigarette smoke- exposed NSCLC cells, preventing EGFR autophosphorylation in the presence of erlotinib. Furthermore, we show that overexpression of a dominant-negative Src (Y527F/K295R) restores TKI sensitivity to A549 exposed to cigarette smoke. Importantly, the TKI resistance that emerges even in cigarette smoke-exposed L858R EGFR-expressing NSCLC cells could be eliminated with Src inhibition. Together, these findings offer new rationale for using Src inhibitors for treating TKI-resistant NSCLC commonly observed in smokers. Mol Cancer Ther; 12(8); 1579-90.

Original languageEnglish (US)
Pages (from-to)1579-1590
Number of pages12
JournalMolecular Cancer Therapeutics
Volume12
Issue number8
DOIs
StatePublished - Aug 2013

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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