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Prognostic significance of osteopontin expression in early-stage non-small-cell lung cancer
Osteopontin (OPN) is a multifunctional protein, which has recently been shown to be linked to tumorigenesis, progression and metastasis in different malignancies. Since non-small-cell lung cancer (NSCLC)'s prognosis remains bad, with few predictors of outcome, the purpose of this study was to e...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2005
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361587/ https://www.ncbi.nlm.nih.gov/pubmed/16091764 http://dx.doi.org/10.1038/sj.bjc.6602715 |
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author | Boldrini, L Donati, V Dell'Omodarme, M Prati, M C Faviana, P Camacci, T Lucchi, M Mussi, A Santoro, M Basolo, F Fontanini, G |
author_facet | Boldrini, L Donati, V Dell'Omodarme, M Prati, M C Faviana, P Camacci, T Lucchi, M Mussi, A Santoro, M Basolo, F Fontanini, G |
author_sort | Boldrini, L |
collection | PubMed |
description | Osteopontin (OPN) is a multifunctional protein, which has recently been shown to be linked to tumorigenesis, progression and metastasis in different malignancies. Since non-small-cell lung cancer (NSCLC)'s prognosis remains bad, with few predictors of outcome, the purpose of this study was to evaluate if OPN might be involved in NSCLC's biology and therefore represent a prognostic marker and a target for new therapeutic trials. Immunohistochemistry was used to detect OPN expression, evaluated as percentage of neoplastic cells with cytoplasmic immunoreactivity, in a wide cohort of patients with stage I NSCLC (136 cases). The median value of this series (20% of positive cells) was used as the cutoff value to distinguish tumours with low (<20%) from tumours with high (⩾20%) OPN expression. A statistically significant correlation between high levels of OPN and shorter overall (P=0.034) and disease-free (P=0.011) survival in our patients was shown. Our results support the hypothesis that high OPN expression is a significantly unfavourable prognostic factor for the survival of patients with stage I NSCLC. This conclusion has notable importance in terms of the biological characterization of early-stage tumours and therapeutic opportunities. |
format | Text |
id | pubmed-2361587 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23615872009-09-10 Prognostic significance of osteopontin expression in early-stage non-small-cell lung cancer Boldrini, L Donati, V Dell'Omodarme, M Prati, M C Faviana, P Camacci, T Lucchi, M Mussi, A Santoro, M Basolo, F Fontanini, G Br J Cancer Molecular Diagnostics Osteopontin (OPN) is a multifunctional protein, which has recently been shown to be linked to tumorigenesis, progression and metastasis in different malignancies. Since non-small-cell lung cancer (NSCLC)'s prognosis remains bad, with few predictors of outcome, the purpose of this study was to evaluate if OPN might be involved in NSCLC's biology and therefore represent a prognostic marker and a target for new therapeutic trials. Immunohistochemistry was used to detect OPN expression, evaluated as percentage of neoplastic cells with cytoplasmic immunoreactivity, in a wide cohort of patients with stage I NSCLC (136 cases). The median value of this series (20% of positive cells) was used as the cutoff value to distinguish tumours with low (<20%) from tumours with high (⩾20%) OPN expression. A statistically significant correlation between high levels of OPN and shorter overall (P=0.034) and disease-free (P=0.011) survival in our patients was shown. Our results support the hypothesis that high OPN expression is a significantly unfavourable prognostic factor for the survival of patients with stage I NSCLC. This conclusion has notable importance in terms of the biological characterization of early-stage tumours and therapeutic opportunities. Nature Publishing Group 2005-08-22 2005-08-09 /pmc/articles/PMC2361587/ /pubmed/16091764 http://dx.doi.org/10.1038/sj.bjc.6602715 Text en Copyright © 2005 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 Boldrini, L Donati, V Dell'Omodarme, M Prati, M C Faviana, P Camacci, T Lucchi, M Mussi, A Santoro, M Basolo, F Fontanini, G Prognostic significance of osteopontin expression in early-stage non-small-cell lung cancer |
title | Prognostic significance of osteopontin expression in early-stage non-small-cell lung cancer |
title_full | Prognostic significance of osteopontin expression in early-stage non-small-cell lung cancer |
title_fullStr | Prognostic significance of osteopontin expression in early-stage non-small-cell lung cancer |
title_full_unstemmed | Prognostic significance of osteopontin expression in early-stage non-small-cell lung cancer |
title_short | Prognostic significance of osteopontin expression in early-stage non-small-cell lung cancer |
title_sort | prognostic significance of osteopontin expression in early-stage non-small-cell lung cancer |
topic | Molecular Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361587/ https://www.ncbi.nlm.nih.gov/pubmed/16091764 http://dx.doi.org/10.1038/sj.bjc.6602715 |
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