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      <dc:title>NKX2-1 expression as a prognostic marker in early-stage non-small-cell lung cancer</dc:title>
      <dc:creator>Moisés, Jorge</dc:creator>
      <dc:creator>Navarro Ponz, Alfons</dc:creator>
      <dc:creator>Santasusagna, Sandra</dc:creator>
      <dc:creator>Viñolas Segarra, Núria</dc:creator>
      <dc:creator>Molins López-Rodó, Laureano</dc:creator>
      <dc:creator>Ramirez, José</dc:creator>
      <dc:creator>Osorio, Jeisson</dc:creator>
      <dc:creator>Saco, Adela</dc:creator>
      <dc:creator>Castellano, Joan Josep</dc:creator>
      <dc:creator>Muñoz García, Carmen</dc:creator>
      <dc:creator>Morales, Sara</dc:creator>
      <dc:creator>Monzó Planella, Mariano</dc:creator>
      <dc:creator>Marrades Sicart, Ramon Ma.</dc:creator>
      <dc:subject>Càncer de pulmó</dc:subject>
      <dc:subject>Marcadors tumorals</dc:subject>
      <dc:subject>Lung cancer</dc:subject>
      <dc:subject>Tumor markers</dc:subject>
      <dc:description>BACKGROUND: NKX2-1, a key molecule in lung development, is highly expressed in non-small cell lung cancer (NSCLC), particularly in lung adenocarcinoma (ADK), where it is a diagnostic marker. Studies of the prognostic role of NKX2-1 in NSCLC have reported contradictory findings. Two microRNAs (miRNAs) have been associated with NKX2-1: miR-365, which targets NKX2-1; and miR-33a, which is downstream of NKX2-1. We have examined the effect of NKX2-1, miR-365 and miR-33a on survival in a cohort of early-stage NSCLC patients and in sub-groups of patients classified according to the mutational status of TP53, KRAS, and EGFR. METHODS: mRNA and miRNA expression was determined using TaqMan assays in 110 early-stage NSCLC patients. TP53, KRAS, and EGFR mutations were assessed by Sanger sequencing. RESULTS: NKX2-1 expression was upregulated in never-smokers (P = 0.017), ADK (P &lt; 0.0001) and patients with wild-type TP53 (P = 0.001). A negative correlation between NKX2-1 and miR-365 expression was found (ρ = -0.287; P = 0.003) but there was no correlation between NKX2-1 and miR-33a expression. Overall survival (OS) was longer in patients with high expression of NKX2-1 than in those with low expression (80.8 vs 61.2 months (P = 0.035), while a trend towards longer OS was observed in patients with low miR-365 levels (P = 0.07). The impact of NKX2-1 on OS and DFS was higher in patients with neither TP53 nor KRAS mutations. Higher expression of NKX2-1 was related to higher OS (77.6 vs 54 months; P = 0.017) and DFS (74.6 vs 57.7 months; P = 0.006) compared to low expression. The association between NKX2-1 and OS and DFS was strengthened when the analysis was limited to patients with stage I disease (P = 0.005 and P=0.003 respectively). CONCLUSIONS: NKX2-1 expression impacts prognosis in early-stage NSCLC patients, particularly in those with neither TP53 nor KRAS mutations.</dc:description>
      <dc:date>2018-06-12T10:59:36Z</dc:date>
      <dc:date>2018-06-12T10:59:36Z</dc:date>
      <dc:date>2017-12-13</dc:date>
      <dc:date>2018-06-12T10:59:36Z</dc:date>
      <dc:type>info:eu-repo/semantics/article</dc:type>
      <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
      <dc:relation>Reproducció del document publicat a: https://doi.org/10.1186/s12890-017-0542-z</dc:relation>
      <dc:relation>BMC Pulmonary Medicine, 2017, vol. 17, num. 197</dc:relation>
      <dc:relation>https://doi.org/10.1186/s12890-017-0542-z</dc:relation>
      <dc:rights>cc-by (c) Moisés, Jorge et al., 2017</dc:rights>
      <dc:rights>http://creativecommons.org/licenses/by/3.0/es</dc:rights>
      <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
      <dc:publisher>BioMed Central</dc:publisher>
      <dc:source>Articles publicats en revistes (Cirurgia i Especialitats Medicoquirúrgiques)</dc:source>
   </ow:Publication>
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