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TWIST1 a new determinant of epithelial to mesenchymal transition in EGFR mutated lung adenocarcinoma

Metastasis is a multistep process and the main cause of mortality in lung cancer patients. We previously showed that EGFR mutations were associated with a copy number gain at a locus encompassing the TWIST1 gene on chromosome 7. TWIST1 is a highly conserved developmental gene involved in embryogenes...

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Published in:PloS one 2012-01, Vol.7 (1), p.e29954-e29954
Main Authors: Pallier, Karine, Cessot, Anatole, Côté, Jean-Francois, Just, Pierre-Alexandre, Cazes, Aurélie, Fabre, Elizabeth, Danel, Claire, Riquet, Marc, Devouassoux-Shisheboran, Mojgan, Ansieau, Stéphane, Puisieux, Alain, Laurent-Puig, Pierre, Blons, Hélène
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Language:English
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Summary:Metastasis is a multistep process and the main cause of mortality in lung cancer patients. We previously showed that EGFR mutations were associated with a copy number gain at a locus encompassing the TWIST1 gene on chromosome 7. TWIST1 is a highly conserved developmental gene involved in embryogenesis that may be reactivated in cancers promoting both malignant conversion and cancer progression through an epithelial to mesenchymal transition (EMT). The aim of this study was to investigate the possible implication of TWIST1 reactivation on the acquisition of a mesenchymal phenotype in EGFR mutated lung cancer. We studied a series of consecutive lung adenocarcinoma from Caucasian non-smokers for which surgical frozen samples were available (n = 33) and showed that TWIST1 expression was linked to EGFR mutations (P
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0029954