Abstract

<div>Abstract<p><b>Purpose:</b> Lung adenocarcinoma and lung squamous cell carcinoma (SCC) are the most common non–small cell lung cancer (NSCLC) subtypes. This study was designed to determine whether reduced expression of TGFβ type II receptor (<i>TGFβRII</i>) promotes lung adenocarcinoma and SCC carcinogenesis.</p><p><b>Experimental Design:</b> We examined <i>TGFβRII</i> expression at the protein and mRNA levels in human NSCLC samples and assessed the relationship between <i>TGFβRII</i> expression and clinicopathologic parameters. To determine whether sporadic <i>TGFβRII</i> deletion in airway epithelial cells induces NSCLC formation, we targeted <i>TGFβRII</i> deletion alone and in combination with oncogenic Kras<sup>G12D</sup> to murine airways using a keratin 5 (<i>K5</i>) promoter and inducible Cre recombinase.</p><p><b>Results:</b> Reduced <i>TGFβRII</i> expression in human NSCLC is associated with male gender, smoking, SCC histology, reduced differentiation, increased tumor stage, increased nodal metastasis, and reduced survival. Homozygous or heterozygous <i>TGFβRII</i> deletion in mouse airway epithelia increases the size and number of <i>Kras<sup>G12D</sup></i>-initiated adenocarcinoma and SCC. <i>TGFβRII</i> deletion increases proliferation, local inflammation, and TGFβ ligand elaboration; <i>TGFβRII</i> knockdown in airway epithelial cells increases migration and invasion.</p><p><b>Conclusions:</b> Reduced <i>TGFβRII</i> expression in human NSCLC is associated with more aggressive tumor behavior and inflammation that is, at least partially, mediated by increased TGFβ1 expression. <i>TGFβRII</i> deletion in mouse airway epithelial cells promotes adenocarcinoma and SCC formation, indicating that <i>TGFβRII</i> loss plays a causal role in lung carcinogenesis. That <i>TGFβRII</i> shows haploid insufficiency suggests that a 50% TGFβRII protein reduction would negatively impact lung cancer prognosis. <i>Clin Cancer Res; 18(8); 2173–83. ©2012 AACR</i>.</p></div>

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call