Abstract

Therapies targeting SRC family kinases (SFKs) have shown efficacy in treating non-small cell lung cancer (NSCLC). However, recent clinical trials have found that the SFK inhibitor dasatinib is ineffective in some patient cohorts. Regardless, dasatinib treatment may benefit some NSCLC patient subgroups. Here, we investigated whether expression of LYN, a member of the SFK family, is associated with patient survival, the efficacy of dasatinib, and/or NSCLC cell viability. LYN expression was associated with poor overall survival in a multivariate analysis, and this association was strongest in non-smoker female patients with adenocarcinoma (ADC). In lung ADC cells, LYN expression enhanced cell proliferation, migration, and invasion. Dasatinib inhibited LYN activity and decreased cell viability in LYN-positive ADC cell lines and xenografts. Additionally, we identified the SFKs SRC and YES as candidate dasatinib targets in LYN-negative ADC cell lines. Our findings suggest that LYN is a useful prognostic marker and a selective target of dasatinib therapy in the lung ADC subpopulation especially in female non-smokers with lung ADC.

Highlights

  • Lung cancer, the leading cause of cancer-related death worldwide, can be classified as either small cell or non-small cell lung carcinoma (NSCLC)

  • Clinicopathological features of the enrolled non-small cell lung cancer (NSCLC) patients are summarized in Supplementary Table S1 and grouped according to LYN expression status

  • Because LYN expression is associated with clinical outcomes in lung adenocarcinoma, and in patients with ADC in general, we examined the functions of LYN in ADC cell lines

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Summary

Introduction

The leading cause of cancer-related death worldwide, can be classified as either small cell or non-small cell lung carcinoma (NSCLC). NSCLC is often associated with epidermal growth factor receptor (EGFR) overexpression, which occurs in 40%–80% of patients; EGFRtargeting therapies have been investigated [2]. These therapies are effective only in NSCLC patients with activating EGFR mutations; alternative therapies are required to target NSCLCs that do not respond to current treatment regimens [3]. A potent SFKs inhibitor, is currently being evaluated in several clinical trials for use in NSCLC. These studies, which did not consider genetic information, reported that www.impactjournals.com/oncotarget dasatinib was ineffective in their patient cohorts [9,10,11,12]. It is of interest to determine whether certain NSCLC patient subgroups may benefit from dasatinib treatment, either as a monotherapy or in combination with other therapies, compared to NSCLC patients in general

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