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Genetic Classification of Oral and Oropharyngeal Carcinomas Identifies Subgroups with a Different Prognosis

The common risk factors for oral and oropharyngeal cancer are tobacco smoking and alcohol consumption, and recently the human papillomavirus (HPV) was shown to be involved in a subgroup. HPV-positive and -negative carcinomas can be distinguished on basis of their genetic profiles. Aim of this study...

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Autores principales: Smeets, Serge J., Brakenhoff, Ruud H., Ylstrab, Bauke, van Wieringen, Wessel N., van de Wiel, Mark A., Leemans, C. René, Braakhuis, Boudewijn J. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4618915/
https://www.ncbi.nlm.nih.gov/pubmed/19633365
http://dx.doi.org/10.3233/CLO-2009-0471
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author Smeets, Serge J.
Brakenhoff, Ruud H.
Ylstrab, Bauke
van Wieringen, Wessel N.
van de Wiel, Mark A.
Leemans, C. René
Braakhuis, Boudewijn J. M.
author_facet Smeets, Serge J.
Brakenhoff, Ruud H.
Ylstrab, Bauke
van Wieringen, Wessel N.
van de Wiel, Mark A.
Leemans, C. René
Braakhuis, Boudewijn J. M.
author_sort Smeets, Serge J.
collection PubMed
description The common risk factors for oral and oropharyngeal cancer are tobacco smoking and alcohol consumption, and recently the human papillomavirus (HPV) was shown to be involved in a subgroup. HPV-positive and -negative carcinomas can be distinguished on basis of their genetic profiles. Aim of this study was to investigate patterns of chromosomal aberrations of HPV-negative oral and oropharyngeal squamous cell carcinomas (OOSCC) in order to improve stratification of patients regarding outcome. Thirty-nine OOSCCs were classified on basis of their genetic pattern determined by array comparative genomic hybridization (aCGH). Resulting groups were related to patient and tumor characteristics using the Fisher’s exact test and in addition to survival with the Kaplan–Meier and log rank tests. Classification distinguished three groups, one characterized by hardly any chromosomal aberration (N = 8) and another by a relatively high level (N = 26), and one with a very high level (N = 5) of chromosomal aberrations. This classification was significantly (p = 0.003) associated with survival, with the best survival in the genetically ‘silent’ group and the worst survival in the most aberrant group. The silent profile was significantly (p < 0.05) associated with wild-type TP53, an absence of alcohol consumption and a female gender. These carcinomas were negative for microsatellite instability. This classification of OOSCC was confirmed in an independent set of 89 oral carcinomas. In conclusion, the discovery of these new classes of oral and oropharyngeal cancer with unique genetic and clinical characteristics has important consequences for future basic and clinical studies.
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spelling pubmed-46189152016-01-12 Genetic Classification of Oral and Oropharyngeal Carcinomas Identifies Subgroups with a Different Prognosis Smeets, Serge J. Brakenhoff, Ruud H. Ylstrab, Bauke van Wieringen, Wessel N. van de Wiel, Mark A. Leemans, C. René Braakhuis, Boudewijn J. M. Cell Oncol Other The common risk factors for oral and oropharyngeal cancer are tobacco smoking and alcohol consumption, and recently the human papillomavirus (HPV) was shown to be involved in a subgroup. HPV-positive and -negative carcinomas can be distinguished on basis of their genetic profiles. Aim of this study was to investigate patterns of chromosomal aberrations of HPV-negative oral and oropharyngeal squamous cell carcinomas (OOSCC) in order to improve stratification of patients regarding outcome. Thirty-nine OOSCCs were classified on basis of their genetic pattern determined by array comparative genomic hybridization (aCGH). Resulting groups were related to patient and tumor characteristics using the Fisher’s exact test and in addition to survival with the Kaplan–Meier and log rank tests. Classification distinguished three groups, one characterized by hardly any chromosomal aberration (N = 8) and another by a relatively high level (N = 26), and one with a very high level (N = 5) of chromosomal aberrations. This classification was significantly (p = 0.003) associated with survival, with the best survival in the genetically ‘silent’ group and the worst survival in the most aberrant group. The silent profile was significantly (p < 0.05) associated with wild-type TP53, an absence of alcohol consumption and a female gender. These carcinomas were negative for microsatellite instability. This classification of OOSCC was confirmed in an independent set of 89 oral carcinomas. In conclusion, the discovery of these new classes of oral and oropharyngeal cancer with unique genetic and clinical characteristics has important consequences for future basic and clinical studies. IOS Press 2009 2009-07-24 /pmc/articles/PMC4618915/ /pubmed/19633365 http://dx.doi.org/10.3233/CLO-2009-0471 Text en Copyright © 2009 Hindawi Publishing Corporation and the authors.
spellingShingle Other
Smeets, Serge J.
Brakenhoff, Ruud H.
Ylstrab, Bauke
van Wieringen, Wessel N.
van de Wiel, Mark A.
Leemans, C. René
Braakhuis, Boudewijn J. M.
Genetic Classification of Oral and Oropharyngeal Carcinomas Identifies Subgroups with a Different Prognosis
title Genetic Classification of Oral and Oropharyngeal Carcinomas Identifies Subgroups with a Different Prognosis
title_full Genetic Classification of Oral and Oropharyngeal Carcinomas Identifies Subgroups with a Different Prognosis
title_fullStr Genetic Classification of Oral and Oropharyngeal Carcinomas Identifies Subgroups with a Different Prognosis
title_full_unstemmed Genetic Classification of Oral and Oropharyngeal Carcinomas Identifies Subgroups with a Different Prognosis
title_short Genetic Classification of Oral and Oropharyngeal Carcinomas Identifies Subgroups with a Different Prognosis
title_sort genetic classification of oral and oropharyngeal carcinomas identifies subgroups with a different prognosis
topic Other
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4618915/
https://www.ncbi.nlm.nih.gov/pubmed/19633365
http://dx.doi.org/10.3233/CLO-2009-0471
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