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Osteopontin is a marker for cancer aggressiveness and patient survival
BACKGROUND: Only a fraction of molecular cancer markers identified in the scientific literature have found clinical use. Specifically, few predictors of invasiveness are established in diagnostics. Meta-analysis is a valuable tool for biomarker validation. Here, we evaluate Osteopontin as a marker f...
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2966627/ https://www.ncbi.nlm.nih.gov/pubmed/20823889 http://dx.doi.org/10.1038/sj.bjc.6605834 |
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author | Weber, G F Lett, G S Haubein, N C |
author_facet | Weber, G F Lett, G S Haubein, N C |
author_sort | Weber, G F |
collection | PubMed |
description | BACKGROUND: Only a fraction of molecular cancer markers identified in the scientific literature have found clinical use. Specifically, few predictors of invasiveness are established in diagnostics. Meta-analysis is a valuable tool for biomarker validation. Here, we evaluate Osteopontin as a marker for tumor aggressiveness (grade, stage, early progression) and patient survival. METHODS: Publications through 2008 with the keywords ‘osteopontin AND cancer’ were retrieved. Titles and abstracts were screened for studies presenting original data on human subjects. This left 228 publications for data extraction. We applied categorical data analysis for testing the relationship between Osteopontin and a clinical variable. RESULTS: Osteopontin ranks correlated with lower overall and disease-free/relapse-free survival in all tumors combined, as well as in lung cancer, breast cancer, prostate cancer, head and neck cancer, and liver cancer. Further, Osteopontin levels correlated with tumor grade and stage for all tumors combined and for several individual tumor types. Osteopontin levels were significantly associated with the early progression of eight cancers, independent in one, and inversely correlated in two. CONCLUSIONS: Osteopontin is significantly associated with survival in several forms of cancer. Osteopontin levels are also markers for stage, grade, and early tumor progression in multiple cancers, reflecting a common molecular underpinning for distinct clinical measures. Osteopontin has value as a clinical tumor progression marker. |
format | Text |
id | pubmed-2966627 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-29666272011-09-07 Osteopontin is a marker for cancer aggressiveness and patient survival Weber, G F Lett, G S Haubein, N C Br J Cancer Molecular Diagnostics BACKGROUND: Only a fraction of molecular cancer markers identified in the scientific literature have found clinical use. Specifically, few predictors of invasiveness are established in diagnostics. Meta-analysis is a valuable tool for biomarker validation. Here, we evaluate Osteopontin as a marker for tumor aggressiveness (grade, stage, early progression) and patient survival. METHODS: Publications through 2008 with the keywords ‘osteopontin AND cancer’ were retrieved. Titles and abstracts were screened for studies presenting original data on human subjects. This left 228 publications for data extraction. We applied categorical data analysis for testing the relationship between Osteopontin and a clinical variable. RESULTS: Osteopontin ranks correlated with lower overall and disease-free/relapse-free survival in all tumors combined, as well as in lung cancer, breast cancer, prostate cancer, head and neck cancer, and liver cancer. Further, Osteopontin levels correlated with tumor grade and stage for all tumors combined and for several individual tumor types. Osteopontin levels were significantly associated with the early progression of eight cancers, independent in one, and inversely correlated in two. CONCLUSIONS: Osteopontin is significantly associated with survival in several forms of cancer. Osteopontin levels are also markers for stage, grade, and early tumor progression in multiple cancers, reflecting a common molecular underpinning for distinct clinical measures. Osteopontin has value as a clinical tumor progression marker. Nature Publishing Group 2010-09-07 2010-09-07 /pmc/articles/PMC2966627/ /pubmed/20823889 http://dx.doi.org/10.1038/sj.bjc.6605834 Text en Copyright © 2010 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 Weber, G F Lett, G S Haubein, N C Osteopontin is a marker for cancer aggressiveness and patient survival |
title | Osteopontin is a marker for cancer aggressiveness and patient survival |
title_full | Osteopontin is a marker for cancer aggressiveness and patient survival |
title_fullStr | Osteopontin is a marker for cancer aggressiveness and patient survival |
title_full_unstemmed | Osteopontin is a marker for cancer aggressiveness and patient survival |
title_short | Osteopontin is a marker for cancer aggressiveness and patient survival |
title_sort | osteopontin is a marker for cancer aggressiveness and patient survival |
topic | Molecular Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2966627/ https://www.ncbi.nlm.nih.gov/pubmed/20823889 http://dx.doi.org/10.1038/sj.bjc.6605834 |
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