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Identification of new candidate therapeutic target genes in head and neck squamous cell carcinomas
BACKGROUND: We aimed at identifying druggable molecular alterations at the RNA level from untreated HNSCC patients, and assessing their prognostic significance. METHODS: We retrieved 96 HNSCC patients who underwent primary surgery. Real-time quantitative RT-PCR was used to analyze a panel of 42 gene...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5216951/ https://www.ncbi.nlm.nih.gov/pubmed/27329726 http://dx.doi.org/10.18632/oncotarget.10163 |
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author | Sablin, Marie-Paule Dubot, Coraline Klijanienko, Jerzy Vacher, Sophie Ouafi, Lamia Chemlali, Walid Caly, Martial Sastre-Garau, Xavier Lappartient, Emmanuelle Mariani, Odette Rodriguez, José Jouffroy, Thomas Girod, Angélique Calugaru, Valentin Hoffmann, Caroline Lidereau, Rosette Berger, Frédérique Kamal, Maud Bieche, Ivan Le Tourneau, Christophe |
author_facet | Sablin, Marie-Paule Dubot, Coraline Klijanienko, Jerzy Vacher, Sophie Ouafi, Lamia Chemlali, Walid Caly, Martial Sastre-Garau, Xavier Lappartient, Emmanuelle Mariani, Odette Rodriguez, José Jouffroy, Thomas Girod, Angélique Calugaru, Valentin Hoffmann, Caroline Lidereau, Rosette Berger, Frédérique Kamal, Maud Bieche, Ivan Le Tourneau, Christophe |
author_sort | Sablin, Marie-Paule |
collection | PubMed |
description | BACKGROUND: We aimed at identifying druggable molecular alterations at the RNA level from untreated HNSCC patients, and assessing their prognostic significance. METHODS: We retrieved 96 HNSCC patients who underwent primary surgery. Real-time quantitative RT-PCR was used to analyze a panel of 42 genes coding for major druggable proteins. Univariate and multivariate analyses were performed to assess the prognostic significance of overexpressed genes. RESULTS: Median age was 56 years [35–78]. Most of patients were men (80%) with a history of alcohol (70.4%) and/or tobacco consumption (72.5%). Twelve patients (12%) were HPV-positive. Most significantly overexpressed genes involved cell cycle regulation (CCND1 [27%], CDK6 [21%]), tyrosine kinase receptors (MET [18%], EGFR [14%]), angiogenesis (PGF [301%], VEGFA [14%]), and immune system (PDL1/CD274 [28%]). PIK3CA expression was an independent prognostic marker, associated with shorter disease-free survival. CONCLUSIONS: We identified druggable overexpressed genes associated with a poor outcome that might be of interest for personalizing treatment of HNSCC patients. |
format | Online Article Text |
id | pubmed-5216951 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-52169512017-01-17 Identification of new candidate therapeutic target genes in head and neck squamous cell carcinomas Sablin, Marie-Paule Dubot, Coraline Klijanienko, Jerzy Vacher, Sophie Ouafi, Lamia Chemlali, Walid Caly, Martial Sastre-Garau, Xavier Lappartient, Emmanuelle Mariani, Odette Rodriguez, José Jouffroy, Thomas Girod, Angélique Calugaru, Valentin Hoffmann, Caroline Lidereau, Rosette Berger, Frédérique Kamal, Maud Bieche, Ivan Le Tourneau, Christophe Oncotarget Research Paper BACKGROUND: We aimed at identifying druggable molecular alterations at the RNA level from untreated HNSCC patients, and assessing their prognostic significance. METHODS: We retrieved 96 HNSCC patients who underwent primary surgery. Real-time quantitative RT-PCR was used to analyze a panel of 42 genes coding for major druggable proteins. Univariate and multivariate analyses were performed to assess the prognostic significance of overexpressed genes. RESULTS: Median age was 56 years [35–78]. Most of patients were men (80%) with a history of alcohol (70.4%) and/or tobacco consumption (72.5%). Twelve patients (12%) were HPV-positive. Most significantly overexpressed genes involved cell cycle regulation (CCND1 [27%], CDK6 [21%]), tyrosine kinase receptors (MET [18%], EGFR [14%]), angiogenesis (PGF [301%], VEGFA [14%]), and immune system (PDL1/CD274 [28%]). PIK3CA expression was an independent prognostic marker, associated with shorter disease-free survival. CONCLUSIONS: We identified druggable overexpressed genes associated with a poor outcome that might be of interest for personalizing treatment of HNSCC patients. Impact Journals LLC 2016-06-18 /pmc/articles/PMC5216951/ /pubmed/27329726 http://dx.doi.org/10.18632/oncotarget.10163 Text en Copyright: © 2016 Sablin et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Sablin, Marie-Paule Dubot, Coraline Klijanienko, Jerzy Vacher, Sophie Ouafi, Lamia Chemlali, Walid Caly, Martial Sastre-Garau, Xavier Lappartient, Emmanuelle Mariani, Odette Rodriguez, José Jouffroy, Thomas Girod, Angélique Calugaru, Valentin Hoffmann, Caroline Lidereau, Rosette Berger, Frédérique Kamal, Maud Bieche, Ivan Le Tourneau, Christophe Identification of new candidate therapeutic target genes in head and neck squamous cell carcinomas |
title | Identification of new candidate therapeutic target genes in head and neck squamous cell carcinomas |
title_full | Identification of new candidate therapeutic target genes in head and neck squamous cell carcinomas |
title_fullStr | Identification of new candidate therapeutic target genes in head and neck squamous cell carcinomas |
title_full_unstemmed | Identification of new candidate therapeutic target genes in head and neck squamous cell carcinomas |
title_short | Identification of new candidate therapeutic target genes in head and neck squamous cell carcinomas |
title_sort | identification of new candidate therapeutic target genes in head and neck squamous cell carcinomas |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5216951/ https://www.ncbi.nlm.nih.gov/pubmed/27329726 http://dx.doi.org/10.18632/oncotarget.10163 |
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