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FAS/FASL Expression Profile as a Prognostic Marker in Squamous Cell Carcinoma of the Oral Cavity

FAS/FASL altered expression may cause tumor protecting immunomodulation, with a direct impact on patient prognosis. FAS expression was studied in 60 squamous cell carcinomas of the oral cavity. FAS expression did not show a significant association with tumor histopathological characteristics, but wa...

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Autores principales: de Carvalho-Neto, Paulo Bentes, dos Santos, Marcelo, de Carvalho, Marcos Brasilino, Mercante, Ana Maria da Cunha, dos Santos, Viviane Priscila Pina, Severino, Patrícia, Tajara, Eloiza Helena, Louro, Iuri Drumond, da Silva-Conforti, Adriana Madeira Álvares
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3716880/
https://www.ncbi.nlm.nih.gov/pubmed/23894399
http://dx.doi.org/10.1371/journal.pone.0069024
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author de Carvalho-Neto, Paulo Bentes
dos Santos, Marcelo
de Carvalho, Marcos Brasilino
Mercante, Ana Maria da Cunha
dos Santos, Viviane Priscila Pina
Severino, Patrícia
Tajara, Eloiza Helena
Louro, Iuri Drumond
da Silva-Conforti, Adriana Madeira Álvares
author_facet de Carvalho-Neto, Paulo Bentes
dos Santos, Marcelo
de Carvalho, Marcos Brasilino
Mercante, Ana Maria da Cunha
dos Santos, Viviane Priscila Pina
Severino, Patrícia
Tajara, Eloiza Helena
Louro, Iuri Drumond
da Silva-Conforti, Adriana Madeira Álvares
author_sort de Carvalho-Neto, Paulo Bentes
collection PubMed
description FAS/FASL altered expression may cause tumor protecting immunomodulation, with a direct impact on patient prognosis. FAS expression was studied in 60 squamous cell carcinomas of the oral cavity. FAS expression did not show a significant association with tumor histopathological characteristics, but was significantly associated with lymph node positivity. FAS expression was significantly associated with disease specific death and negative FAS expression was an independent risk factor, increasing risk 4 times when compared to positive expression. When FAS and FASL expression results were combined, we were able to define high, intermediate and low risk profiles. Disease-free and disease-specific survival were significantly correlated with FAS/FASL expression profiles. The high risk category was an independent marker for earlier disease relapse and disease-specific death, with approximately 4- and 6-fold increased risk, respectively, when compared to the low risk profile. Risk profiles based on FAS/FASL expression showed that high risk was significantly associated with increased disease relapse and death, as well as shorter disease-free or disease-specific survival. This categorization, added to patient clinical data, may facilitate the choice of therapy, minimizing treatment failure and increasing disease control.
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spelling pubmed-37168802013-07-26 FAS/FASL Expression Profile as a Prognostic Marker in Squamous Cell Carcinoma of the Oral Cavity de Carvalho-Neto, Paulo Bentes dos Santos, Marcelo de Carvalho, Marcos Brasilino Mercante, Ana Maria da Cunha dos Santos, Viviane Priscila Pina Severino, Patrícia Tajara, Eloiza Helena Louro, Iuri Drumond da Silva-Conforti, Adriana Madeira Álvares PLoS One Research Article FAS/FASL altered expression may cause tumor protecting immunomodulation, with a direct impact on patient prognosis. FAS expression was studied in 60 squamous cell carcinomas of the oral cavity. FAS expression did not show a significant association with tumor histopathological characteristics, but was significantly associated with lymph node positivity. FAS expression was significantly associated with disease specific death and negative FAS expression was an independent risk factor, increasing risk 4 times when compared to positive expression. When FAS and FASL expression results were combined, we were able to define high, intermediate and low risk profiles. Disease-free and disease-specific survival were significantly correlated with FAS/FASL expression profiles. The high risk category was an independent marker for earlier disease relapse and disease-specific death, with approximately 4- and 6-fold increased risk, respectively, when compared to the low risk profile. Risk profiles based on FAS/FASL expression showed that high risk was significantly associated with increased disease relapse and death, as well as shorter disease-free or disease-specific survival. This categorization, added to patient clinical data, may facilitate the choice of therapy, minimizing treatment failure and increasing disease control. Public Library of Science 2013-07-19 /pmc/articles/PMC3716880/ /pubmed/23894399 http://dx.doi.org/10.1371/journal.pone.0069024 Text en © 2013 de Carvalho-Neto et al http://creativecommons.org/licenses/by/4.0/ 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 properly credited.
spellingShingle Research Article
de Carvalho-Neto, Paulo Bentes
dos Santos, Marcelo
de Carvalho, Marcos Brasilino
Mercante, Ana Maria da Cunha
dos Santos, Viviane Priscila Pina
Severino, Patrícia
Tajara, Eloiza Helena
Louro, Iuri Drumond
da Silva-Conforti, Adriana Madeira Álvares
FAS/FASL Expression Profile as a Prognostic Marker in Squamous Cell Carcinoma of the Oral Cavity
title FAS/FASL Expression Profile as a Prognostic Marker in Squamous Cell Carcinoma of the Oral Cavity
title_full FAS/FASL Expression Profile as a Prognostic Marker in Squamous Cell Carcinoma of the Oral Cavity
title_fullStr FAS/FASL Expression Profile as a Prognostic Marker in Squamous Cell Carcinoma of the Oral Cavity
title_full_unstemmed FAS/FASL Expression Profile as a Prognostic Marker in Squamous Cell Carcinoma of the Oral Cavity
title_short FAS/FASL Expression Profile as a Prognostic Marker in Squamous Cell Carcinoma of the Oral Cavity
title_sort fas/fasl expression profile as a prognostic marker in squamous cell carcinoma of the oral cavity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3716880/
https://www.ncbi.nlm.nih.gov/pubmed/23894399
http://dx.doi.org/10.1371/journal.pone.0069024
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