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SNAI2 and TWIST1 in lymph node progression in early stages of NSCLC patients.
Emprou, Camille; Le Van Quyen, Pauline; Jégu, Jérémie; Prim, Nathalie; Weingertner, Noëlle; Guérin, Eric; Pencreach, Erwan; Legrain, Michèle; Voegeli, Anne-Claire; Leduc, Charlotte; Mennecier, Bertrand; Falcoz, Pierre-Emmanuel; Olland, Anne; Santelmo, Nicolas; Quoix, Elisabeth; Massard, Gilbert; Guenot, Dominique; Chenard, Marie-Pierre; Beau-Faller, Michèle.
Afiliação
  • Emprou C; Department of Pathology, Hôpital de Hautepierre, University Hospital of Strasbourg, Strasbourg, France.
  • Le Van Quyen P; Department of Pathology, Hôpital de Hautepierre, University Hospital of Strasbourg, Strasbourg, France.
  • Jégu J; Department of Public Health, Nouvel Hôpital Civil, University Hospital of Strasbourg, Strasbourg, France.
  • Prim N; EA3430: Tumoral Progression and Micro-environment, Translational and Epidemiological Approaches, Université de Strasbourg, Strasbourg, France.
  • Weingertner N; Department of Pneumology, Nouvel Hôpital Civil, University Hospital of Strasbourg, Strasbourg, France.
  • Guérin E; Department of Pathology, Hôpital de Hautepierre, University Hospital of Strasbourg, Strasbourg, France.
  • Pencreach E; EA3430: Tumoral Progression and Micro-environment, Translational and Epidemiological Approaches, Université de Strasbourg, Strasbourg, France.
  • Legrain M; Department of Molecular Biology, Oncobiology Laboratory, Regional Institute of Cancer Strasbourg, Hôpital de Hautepierre, University Hospital of Strasbourg, Strasbourg, France.
  • Voegeli AC; EA3430: Tumoral Progression and Micro-environment, Translational and Epidemiological Approaches, Université de Strasbourg, Strasbourg, France.
  • Leduc C; Department of Molecular Biology, Oncobiology Laboratory, Regional Institute of Cancer Strasbourg, Hôpital de Hautepierre, University Hospital of Strasbourg, Strasbourg, France.
  • Mennecier B; Department of Molecular Biology, Oncobiology Laboratory, Regional Institute of Cancer Strasbourg, Hôpital de Hautepierre, University Hospital of Strasbourg, Strasbourg, France.
  • Falcoz PE; Department of Molecular Biology, Oncobiology Laboratory, Regional Institute of Cancer Strasbourg, Hôpital de Hautepierre, University Hospital of Strasbourg, Strasbourg, France.
  • Olland A; Department of Pneumology, Nouvel Hôpital Civil, University Hospital of Strasbourg, Strasbourg, France.
  • Santelmo N; Department of Pneumology, Nouvel Hôpital Civil, University Hospital of Strasbourg, Strasbourg, France.
  • Quoix E; Department of Thoracic Surgery, Nouvel Hôpital Civil, University Hospital of Strasbourg, Strasbourg, France.
  • Massard G; Department of Thoracic Surgery, Nouvel Hôpital Civil, University Hospital of Strasbourg, Strasbourg, France.
  • Guenot D; Department of Thoracic Surgery, Nouvel Hôpital Civil, University Hospital of Strasbourg, Strasbourg, France.
  • Chenard MP; Department of Pneumology, Nouvel Hôpital Civil, University Hospital of Strasbourg, Strasbourg, France.
  • Beau-Faller M; Department of Thoracic Surgery, Nouvel Hôpital Civil, University Hospital of Strasbourg, Strasbourg, France.
Cancer Med ; 7(7): 3278-3291, 2018 Jul.
Article em En | MEDLINE | ID: mdl-29845746
Lymph node metastasis is an important prognosis factor in non-small cell lung cancer (NSCLC) patients. The aim of this study was to investigate the role of epithelial to mesenchymal transition (EMT) in lymph node progression in the early stages of NSCLC. We studied a retrospective cohort of 160 consecutive surgically treated NSCLC patients with available frozen tumor samples for expression of EMT markers (CDH1, CTNNB1, CDH2, and VIMENTIN), inducers (TGFB1, c-MET, and CAIX), and transcription factors (EMT-TF: SNAI1, SNAI2, ZEB1, TWIST1, and TWIST2). Partial EMT was more frequent in N1-2 (N+) vs N0 patients (P < .01). TGFB1 (P = .02) as well as SNAI2 (P < .01) and TWIST1 (P = .04) were the most differentially expressed genes in N+ tumors. In this group, ZEB1 was correlated with all EMT inducers and other EMT-TFs were overexpressed depending on the inducers. CAIX was an independent prognostic factor for overall survival (IC 95% HR: 1.10-5.14, P = .03). Partial EMT is involved in lymph node progression of NSCLC patients and depends on the TGFß pathway. EMT-TFs are differentially expressed depending on EMT inducers. CAIX might be a relevant prognostic marker in early stage NSCLC.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2018 Tipo de documento: Article