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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...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
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
Descripción
Sumario: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.