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Epithelial to mesenchymal transition and HPV infection in squamous cell oropharyngeal carcinomas: the papillophar study.

Authors :
Lefevre, Marine
Rousseau, Alexandra
Rayon, Thomas
Dalstein, Véronique
Clavel, Christine
Beby-Defaux, Agnès
Pretet, Jean-Luc
Soussan, Patrick
Polette, Myriam
Lacau Saint Guily, Jean
Birembaut, Philippe
Dalstein, Véronique
Beby-Defaux, Agnès
Papillophar Study Group
Source :
British Journal of Cancer; 1/31/2017, Vol. 116 Issue 3, p362-369, 8p, 1 Color Photograph, 3 Charts, 1 Graph
Publication Year :
2017

Abstract

<bold>Background: </bold>Human Papillomavirus (HPV) infection is recognised as aetiological factor of carcinogenesis in oropharyngeal squamous cell carcinomas (OPC). HPV-related OPC respond better to treatments and have a significantly favourable outcome. Epithelial to mesenchymal transition (EMT) implicated in tumour invasion, is a hallmark of a poor prognosis in carcinomas.<bold>Methods: </bold>We have studied the relationship of EMT markers (E-cadherin, β-catenin and vimentin) with HPV infection (DNA and E6/E7 mRNA detection), p16INK4a expression and survival outcomes in a cohort of 296 patients with OPC.<bold>Results: </bold>Among the 296 OPSSC, 26% were HPV positive, 20.3% had overt EMT (>25% of vimentin positive tumour cells). Lower E-cadherin expression was associated with a higher risk of distant metastasis in univariate (P=0.0110) and multivariate analyses (hazard ratios (HR)=6.86 (1.98; 23.84)). Vimentin expression tends towards worse metastasis-free survival (MFS; HR=2.53 (1.00; 6.41)) and was an independent prognostic factor of progression-free survival (HR=1.55 (1.03; 2.34)).<bold>Conclusions: </bold>There was a non significant association of EMT with HPV status. This may be explained by a mixed subpopulation of patients HPV positive with associated risk factors (HPV, tobacco and alcohol). Thus, the detection of EMT in OPC represents another reliable approach in the prognosis and the management of OPC whatever their HPV status. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00070920
Volume :
116
Issue :
3
Database :
Complementary Index
Journal :
British Journal of Cancer
Publication Type :
Academic Journal
Accession number :
121032624
Full Text :
https://doi.org/10.1038/bjc.2016.434