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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.
Afiliação
  • Sablin MP; Department of Medical Oncology, Institut Curie, Paris and Saint-Cloud, France.
  • Dubot C; Department of Medical Oncology, Institut Curie, Paris and Saint-Cloud, France.
  • Klijanienko J; Unit of Pharmacogenomics, Department of Genetics, Institut Curie, Paris, France.
  • Vacher S; Department of Biopathology, Institut Curie, Paris, France.
  • Ouafi L; Unit of Pharmacogenomics, Department of Genetics, Institut Curie, Paris, France.
  • Chemlali W; Department of Biopathology, Institut Curie, Paris, France.
  • Caly M; Unit of Pharmacogenomics, Department of Genetics, Institut Curie, Paris, France.
  • Sastre-Garau X; Department of Biopathology, Institut Curie, Paris, France.
  • Lappartient E; Department of Biopathology, Institut Curie, Paris, France.
  • Mariani O; Department of Biopathology, Institut Curie, Paris, France.
  • Rodriguez J; Department of Biopathology, Institut Curie, Paris, France.
  • Jouffroy T; Department of Surgery, Institut Curie, Paris, France.
  • Girod A; Department of Surgery, Institut Curie, Paris, France.
  • Calugaru V; Department of Surgery, Institut Curie, Paris, France.
  • Hoffmann C; Department of Radiotherapy, Institut Curie, Paris, France.
  • Lidereau R; Department of Surgery, Institut Curie, Paris, France.
  • Berger F; Unit of Pharmacogenomics, Department of Genetics, Institut Curie, Paris, France.
  • Kamal M; Department of Surgery, Institut Curie, Paris, France.
  • Bieche I; Department of Biostatistics, Institut Curie, Paris, France.
  • Le Tourneau C; Department of Medical Oncology, Institut Curie, Paris and Saint-Cloud, France.
Oncotarget ; 7(30): 47418-47430, 2016 Jul 26.
Article em En | MEDLINE | ID: mdl-27329726
ABSTRACT

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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma de Células Escamosas / Neoplasias de Cabeça e Pescoço Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma de Células Escamosas / Neoplasias de Cabeça e Pescoço Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2016 Tipo de documento: Article