Inhibitor-sensitive FGFR1 amplification in human non-small cell lung cancer.

PLoS One
Authors
Keywords
Abstract

BACKGROUND: Squamous cell lung carcinomas account for approximately 25% of new lung carcinoma cases and 40,000 deaths per year in the United States. Although there are multiple genomically targeted therapies for lung adenocarcinoma, none has yet been reported in squamous cell lung carcinoma.

METHODOLOGY/PRINCIPAL FINDINGS: Using SNP array analysis, we found that a region of chromosome segment 8p11-12 containing three genes-WHSC1L1, LETM2, and FGFR1-is amplified in 3% of lung adenocarcinomas and 21% of squamous cell lung carcinomas. Furthermore, we demonstrated that a non-small cell lung carcinoma cell line harboring focal amplification of FGFR1 is dependent on FGFR1 activity for cell growth, as treatment of this cell line either with FGFR1-specific shRNAs or with FGFR small molecule enzymatic inhibitors leads to cell growth inhibition.

CONCLUSIONS/SIGNIFICANCE: These studies show that FGFR1 amplification is common in squamous cell lung cancer, and that FGFR1 may represent a promising therapeutic target in non-small cell lung cancer.

Year of Publication
2011
Journal
PLoS One
Volume
6
Issue
6
Pages
e20351
Date Published
2011
ISSN
1932-6203
DOI
10.1371/journal.pone.0020351
PubMed ID
21666749
PubMed Central ID
PMC3110189
Links
Grant list
T32 CA009172 / CA / NCI NIH HHS / United States
T32 GM007753 / GM / NIGMS NIH HHS / United States