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High CIP2A immunoreactivity is an independent prognostic indicator in early-stage tongue cancer
BACKGROUND: No reliable prognostic markers exist for squamous cell carcinoma of the tongue, and its prognosis can even in early stages be unpredictable and survival poor despite treatment. A potential marker is oncoprotein cancerous inhibitor of PP2A (CIP2A), which acts as a prognostic marker in gas...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3111200/ https://www.ncbi.nlm.nih.gov/pubmed/21610708 http://dx.doi.org/10.1038/bjc.2011.167 |
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author | Böckelman, C Hagström, J Mäkinen, L K Keski-Säntti, H Häyry, V Lundin, J Atula, T Ristimäki, A Haglund, C |
author_facet | Böckelman, C Hagström, J Mäkinen, L K Keski-Säntti, H Häyry, V Lundin, J Atula, T Ristimäki, A Haglund, C |
author_sort | Böckelman, C |
collection | PubMed |
description | BACKGROUND: No reliable prognostic markers exist for squamous cell carcinoma of the tongue, and its prognosis can even in early stages be unpredictable and survival poor despite treatment. A potential marker is oncoprotein cancerous inhibitor of PP2A (CIP2A), which acts as a prognostic marker in gastric and non-small cell lung cancers. METHODS: We collected specimens of 73 stage T1N0M0 and T2N0M0 oral squamous cell carcinomas of the tongue, as well as samples from normal oral mucosa, dysplastic lesions, and invasive carcinomas (n=39). All samples were stained for CIP2A by immunohistochemistry. Survival curves were constructed according to the Kaplan–Meier method. The Cox proportional hazard model served for univariate and multivariate survival analysis. RESULTS: High CIP2A immunoreactivity predicted poor survival in tongue cancer patients (P=0.027, logrank test). In multivariate survival analysis, CIP2A was an independent prognostic factor (HR 2.02, 95% confidence interval 1.07–3.82, P=0.030). Cytoplasmic CIP2A expression was higher in severe dysplasia than in mild dysplasia. CONCLUSION: Our results suggest that high CIP2A expression characterises aggressive disease. Acting as a prognostic marker it might be of help when choosing patients for adjuvant treatment in tongue cancer patients. |
format | Online Article Text |
id | pubmed-3111200 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-31112002012-06-07 High CIP2A immunoreactivity is an independent prognostic indicator in early-stage tongue cancer Böckelman, C Hagström, J Mäkinen, L K Keski-Säntti, H Häyry, V Lundin, J Atula, T Ristimäki, A Haglund, C Br J Cancer Molecular Diagnostics BACKGROUND: No reliable prognostic markers exist for squamous cell carcinoma of the tongue, and its prognosis can even in early stages be unpredictable and survival poor despite treatment. A potential marker is oncoprotein cancerous inhibitor of PP2A (CIP2A), which acts as a prognostic marker in gastric and non-small cell lung cancers. METHODS: We collected specimens of 73 stage T1N0M0 and T2N0M0 oral squamous cell carcinomas of the tongue, as well as samples from normal oral mucosa, dysplastic lesions, and invasive carcinomas (n=39). All samples were stained for CIP2A by immunohistochemistry. Survival curves were constructed according to the Kaplan–Meier method. The Cox proportional hazard model served for univariate and multivariate survival analysis. RESULTS: High CIP2A immunoreactivity predicted poor survival in tongue cancer patients (P=0.027, logrank test). In multivariate survival analysis, CIP2A was an independent prognostic factor (HR 2.02, 95% confidence interval 1.07–3.82, P=0.030). Cytoplasmic CIP2A expression was higher in severe dysplasia than in mild dysplasia. CONCLUSION: Our results suggest that high CIP2A expression characterises aggressive disease. Acting as a prognostic marker it might be of help when choosing patients for adjuvant treatment in tongue cancer patients. Nature Publishing Group 2011-06-07 2011-05-24 /pmc/articles/PMC3111200/ /pubmed/21610708 http://dx.doi.org/10.1038/bjc.2011.167 Text en Copyright © 2011 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Molecular Diagnostics Böckelman, C Hagström, J Mäkinen, L K Keski-Säntti, H Häyry, V Lundin, J Atula, T Ristimäki, A Haglund, C High CIP2A immunoreactivity is an independent prognostic indicator in early-stage tongue cancer |
title | High CIP2A immunoreactivity is an independent prognostic indicator in early-stage tongue cancer |
title_full | High CIP2A immunoreactivity is an independent prognostic indicator in early-stage tongue cancer |
title_fullStr | High CIP2A immunoreactivity is an independent prognostic indicator in early-stage tongue cancer |
title_full_unstemmed | High CIP2A immunoreactivity is an independent prognostic indicator in early-stage tongue cancer |
title_short | High CIP2A immunoreactivity is an independent prognostic indicator in early-stage tongue cancer |
title_sort | high cip2a immunoreactivity is an independent prognostic indicator in early-stage tongue cancer |
topic | Molecular Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3111200/ https://www.ncbi.nlm.nih.gov/pubmed/21610708 http://dx.doi.org/10.1038/bjc.2011.167 |
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