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SNAI2 and TWIST1 in lymph node progression in early stages of NSCLC patients

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 cons...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6051239/
https://www.ncbi.nlm.nih.gov/pubmed/29845746
http://dx.doi.org/10.1002/cam4.1545
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author 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
author_facet 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
author_sort Emprou, Camille
collection PubMed
description 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 TGFβ 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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spelling pubmed-60512392018-07-20 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 Cancer Med Cancer Biology 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 TGFβ pathway. EMT‐TFs are differentially expressed depending on EMT inducers. CAIX might be a relevant prognostic marker in early stage NSCLC. John Wiley and Sons Inc. 2018-05-29 /pmc/articles/PMC6051239/ /pubmed/29845746 http://dx.doi.org/10.1002/cam4.1545 Text en © 2018 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Cancer Biology
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
SNAI2 and TWIST1 in lymph node progression in early stages of NSCLC patients
title SNAI2 and TWIST1 in lymph node progression in early stages of NSCLC patients
title_full SNAI2 and TWIST1 in lymph node progression in early stages of NSCLC patients
title_fullStr SNAI2 and TWIST1 in lymph node progression in early stages of NSCLC patients
title_full_unstemmed SNAI2 and TWIST1 in lymph node progression in early stages of NSCLC patients
title_short SNAI2 and TWIST1 in lymph node progression in early stages of NSCLC patients
title_sort snai2 and twist1 in lymph node progression in early stages of nsclc patients
topic Cancer Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6051239/
https://www.ncbi.nlm.nih.gov/pubmed/29845746
http://dx.doi.org/10.1002/cam4.1545
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