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Prognostic significance of cell cycle-associated proteins p16, pRB, cyclin D1 and p53 in resected oropharyngeal carcinoma
BACKGROUND: Human papillomavirus (HPV)-related oropharyngeal squamous cell carcinoma (OPSCC) has an improved outcome and may allow for treatment de-escalation. High-risk HPV (HR-HPV) infection is associated with deregulated expression of the cell cycle-associated proteins p16(INK4), pRB, cyclin D1 a...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6127938/ https://www.ncbi.nlm.nih.gov/pubmed/30189895 http://dx.doi.org/10.1186/s40463-018-0298-3 |
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author | Plath, Michaela Broglie, Martina A. Förbs, Diana Stoeckli, Sandro J. Jochum, Wolfram |
author_facet | Plath, Michaela Broglie, Martina A. Förbs, Diana Stoeckli, Sandro J. Jochum, Wolfram |
author_sort | Plath, Michaela |
collection | PubMed |
description | BACKGROUND: Human papillomavirus (HPV)-related oropharyngeal squamous cell carcinoma (OPSCC) has an improved outcome and may allow for treatment de-escalation. High-risk HPV (HR-HPV) infection is associated with deregulated expression of the cell cycle-associated proteins p16(INK4), pRB, cyclin D1 and p53. The objective of this study was to assess cell cycle proteins as potential surrogate markers for HR-HPV DNA testing to identify OPSCC with favorable prognosis after resection. METHODS: Tissue microarray cores of 313 surgically treated OPSCC were stained for p16(INK4a), pRB, cyclin D1 and p53 using immunohistochemistry. Protein expression was scored as high or low based on the proportion of positive carcinoma cells. Tumor samples were analysed for HR-HPV DNA with polymerase chain reaction-based testing. Associations between cell cycle protein expression and HR-HPV DNA status were evaluated by calculating sensitivity, specificity, predictive values, and diagnostic odds ratios (DOR). Kaplan-Meier and Cox regression analysis were applied to evaluate associations between cell cycle protein expression and patient outcome. RESULTS: High expression of p16(INK4a), cyclin D1, pRB and p53 in tumor cells were observed in 51.8%, 51.4%, 41.9% and 33.5% of OPSCC, respectively. HR-HPV DNA positive were 158/313 (50.5%) tumor samples (HPV16: 147, HPV18: 1, HPV33: 5, HPV35: 2, HPV56: 2, and HPV59: 1). P16(INK4a) showed a higher DOR to predict HR-HPV DNA positivity than pRB, cyclin D1 and p53. Both the p16(INK4a)/pRB and the p16(INK4a)/pRB/cyclin D1/p53 signatures had lower DOR than p16(INK4a) alone. Improved 5-year overall and disease-specific survival were associated with HR-HPV DNA positivity, high p16(INK4a), low pRB, low cyclin D1, and low p53 expression. Associations with improved outcome were also observed for the marker combinations high p16(INK4a)/positive HR-HPV DNA, high p16(INK4a)/low pRB and high p16(INK4a)/low pRB/low cyclin D1/low p53. In a multivariate analysis adjusted for age, smoking history, pT and pN category, high p16(INK4a) expression showed the lowest hazard ratio for death. CONCLUSIONS: High p16(INK4a) expression is a reliable marker for survival prognostication in surgically treated OPSCC patients. Protein signatures including the pRB, cyclin D1 and p53 proteins do not further increase the prognostic performance of p16(INK4a) as a single marker. |
format | Online Article Text |
id | pubmed-6127938 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61279382018-09-10 Prognostic significance of cell cycle-associated proteins p16, pRB, cyclin D1 and p53 in resected oropharyngeal carcinoma Plath, Michaela Broglie, Martina A. Förbs, Diana Stoeckli, Sandro J. Jochum, Wolfram J Otolaryngol Head Neck Surg Original Research Article BACKGROUND: Human papillomavirus (HPV)-related oropharyngeal squamous cell carcinoma (OPSCC) has an improved outcome and may allow for treatment de-escalation. High-risk HPV (HR-HPV) infection is associated with deregulated expression of the cell cycle-associated proteins p16(INK4), pRB, cyclin D1 and p53. The objective of this study was to assess cell cycle proteins as potential surrogate markers for HR-HPV DNA testing to identify OPSCC with favorable prognosis after resection. METHODS: Tissue microarray cores of 313 surgically treated OPSCC were stained for p16(INK4a), pRB, cyclin D1 and p53 using immunohistochemistry. Protein expression was scored as high or low based on the proportion of positive carcinoma cells. Tumor samples were analysed for HR-HPV DNA with polymerase chain reaction-based testing. Associations between cell cycle protein expression and HR-HPV DNA status were evaluated by calculating sensitivity, specificity, predictive values, and diagnostic odds ratios (DOR). Kaplan-Meier and Cox regression analysis were applied to evaluate associations between cell cycle protein expression and patient outcome. RESULTS: High expression of p16(INK4a), cyclin D1, pRB and p53 in tumor cells were observed in 51.8%, 51.4%, 41.9% and 33.5% of OPSCC, respectively. HR-HPV DNA positive were 158/313 (50.5%) tumor samples (HPV16: 147, HPV18: 1, HPV33: 5, HPV35: 2, HPV56: 2, and HPV59: 1). P16(INK4a) showed a higher DOR to predict HR-HPV DNA positivity than pRB, cyclin D1 and p53. Both the p16(INK4a)/pRB and the p16(INK4a)/pRB/cyclin D1/p53 signatures had lower DOR than p16(INK4a) alone. Improved 5-year overall and disease-specific survival were associated with HR-HPV DNA positivity, high p16(INK4a), low pRB, low cyclin D1, and low p53 expression. Associations with improved outcome were also observed for the marker combinations high p16(INK4a)/positive HR-HPV DNA, high p16(INK4a)/low pRB and high p16(INK4a)/low pRB/low cyclin D1/low p53. In a multivariate analysis adjusted for age, smoking history, pT and pN category, high p16(INK4a) expression showed the lowest hazard ratio for death. CONCLUSIONS: High p16(INK4a) expression is a reliable marker for survival prognostication in surgically treated OPSCC patients. Protein signatures including the pRB, cyclin D1 and p53 proteins do not further increase the prognostic performance of p16(INK4a) as a single marker. BioMed Central 2018-09-06 /pmc/articles/PMC6127938/ /pubmed/30189895 http://dx.doi.org/10.1186/s40463-018-0298-3 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Original Research Article Plath, Michaela Broglie, Martina A. Förbs, Diana Stoeckli, Sandro J. Jochum, Wolfram Prognostic significance of cell cycle-associated proteins p16, pRB, cyclin D1 and p53 in resected oropharyngeal carcinoma |
title | Prognostic significance of cell cycle-associated proteins p16, pRB, cyclin D1 and p53 in resected oropharyngeal carcinoma |
title_full | Prognostic significance of cell cycle-associated proteins p16, pRB, cyclin D1 and p53 in resected oropharyngeal carcinoma |
title_fullStr | Prognostic significance of cell cycle-associated proteins p16, pRB, cyclin D1 and p53 in resected oropharyngeal carcinoma |
title_full_unstemmed | Prognostic significance of cell cycle-associated proteins p16, pRB, cyclin D1 and p53 in resected oropharyngeal carcinoma |
title_short | Prognostic significance of cell cycle-associated proteins p16, pRB, cyclin D1 and p53 in resected oropharyngeal carcinoma |
title_sort | prognostic significance of cell cycle-associated proteins p16, prb, cyclin d1 and p53 in resected oropharyngeal carcinoma |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6127938/ https://www.ncbi.nlm.nih.gov/pubmed/30189895 http://dx.doi.org/10.1186/s40463-018-0298-3 |
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