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Plasma osteopontin levels in patients with head and neck cancer and cervix cancer are critically dependent on the choice of ELISA system

BACKGROUND: The tumor-associated glycoprotein osteopontin (OPN) is discussed as a plasma surrogate marker of tumor hypoxia and as an indicator of the presence of pleural mesothelioma in asbestos-exposed individuals. The clinical introduction of plasma OPN measurements requires the availability of a...

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Autores principales: Vordermark, Dirk, Said, Harun M, Katzer, Astrid, Kuhnt, Thomas, Hänsgen, Gabriele, Dunst, Jürgen, Flentje, Michael, Bache, Matthias
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1564036/
https://www.ncbi.nlm.nih.gov/pubmed/16911785
http://dx.doi.org/10.1186/1471-2407-6-207
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author Vordermark, Dirk
Said, Harun M
Katzer, Astrid
Kuhnt, Thomas
Hänsgen, Gabriele
Dunst, Jürgen
Flentje, Michael
Bache, Matthias
author_facet Vordermark, Dirk
Said, Harun M
Katzer, Astrid
Kuhnt, Thomas
Hänsgen, Gabriele
Dunst, Jürgen
Flentje, Michael
Bache, Matthias
author_sort Vordermark, Dirk
collection PubMed
description BACKGROUND: The tumor-associated glycoprotein osteopontin (OPN) is discussed as a plasma surrogate marker of tumor hypoxia and as an indicator of the presence of pleural mesothelioma in asbestos-exposed individuals. The clinical introduction of plasma OPN measurements requires the availability of a reliable enzyme-linked immunosorbence assay (ELISA). METHODS: We compared previously described and currently available ELISA systems on 88 archival plasma samples obtained from patients with head and neck or cervix cancer between 20 days before and 171 after the start of radiotherapy. RESULTS: Median (range) plasma OPN levels were 667 (148.8–2095) ng/ml and 9.8 (3.5–189.5) ng/ml for a previously described and a newly marketed assay, respectively. Although results for different assays were significantly correlated (r = 0.38, p < 0.05, Spearman rank test), between-assay factors ranged from 2.0 to 217.9 (median 74.6) in individual patients. OPN levels in cervix cancer patients were comparable to those of head and neck cancer patients. CONCLUSION: Commercially available OPN ELISA systems produce different absolute plasma OPN levels, compromising a comparison of individual patient data with published results. However, different assays appear to have a similar capacity to rank patients according to plasma OPN level. A review of literature data suggests that plasma OPN levels measured even with identical ELISA systems can only be compared with caution.
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spelling pubmed-15640362006-09-12 Plasma osteopontin levels in patients with head and neck cancer and cervix cancer are critically dependent on the choice of ELISA system Vordermark, Dirk Said, Harun M Katzer, Astrid Kuhnt, Thomas Hänsgen, Gabriele Dunst, Jürgen Flentje, Michael Bache, Matthias BMC Cancer Research Article BACKGROUND: The tumor-associated glycoprotein osteopontin (OPN) is discussed as a plasma surrogate marker of tumor hypoxia and as an indicator of the presence of pleural mesothelioma in asbestos-exposed individuals. The clinical introduction of plasma OPN measurements requires the availability of a reliable enzyme-linked immunosorbence assay (ELISA). METHODS: We compared previously described and currently available ELISA systems on 88 archival plasma samples obtained from patients with head and neck or cervix cancer between 20 days before and 171 after the start of radiotherapy. RESULTS: Median (range) plasma OPN levels were 667 (148.8–2095) ng/ml and 9.8 (3.5–189.5) ng/ml for a previously described and a newly marketed assay, respectively. Although results for different assays were significantly correlated (r = 0.38, p < 0.05, Spearman rank test), between-assay factors ranged from 2.0 to 217.9 (median 74.6) in individual patients. OPN levels in cervix cancer patients were comparable to those of head and neck cancer patients. CONCLUSION: Commercially available OPN ELISA systems produce different absolute plasma OPN levels, compromising a comparison of individual patient data with published results. However, different assays appear to have a similar capacity to rank patients according to plasma OPN level. A review of literature data suggests that plasma OPN levels measured even with identical ELISA systems can only be compared with caution. BioMed Central 2006-08-15 /pmc/articles/PMC1564036/ /pubmed/16911785 http://dx.doi.org/10.1186/1471-2407-6-207 Text en Copyright © 2006 Vordermark et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Vordermark, Dirk
Said, Harun M
Katzer, Astrid
Kuhnt, Thomas
Hänsgen, Gabriele
Dunst, Jürgen
Flentje, Michael
Bache, Matthias
Plasma osteopontin levels in patients with head and neck cancer and cervix cancer are critically dependent on the choice of ELISA system
title Plasma osteopontin levels in patients with head and neck cancer and cervix cancer are critically dependent on the choice of ELISA system
title_full Plasma osteopontin levels in patients with head and neck cancer and cervix cancer are critically dependent on the choice of ELISA system
title_fullStr Plasma osteopontin levels in patients with head and neck cancer and cervix cancer are critically dependent on the choice of ELISA system
title_full_unstemmed Plasma osteopontin levels in patients with head and neck cancer and cervix cancer are critically dependent on the choice of ELISA system
title_short Plasma osteopontin levels in patients with head and neck cancer and cervix cancer are critically dependent on the choice of ELISA system
title_sort plasma osteopontin levels in patients with head and neck cancer and cervix cancer are critically dependent on the choice of elisa system
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1564036/
https://www.ncbi.nlm.nih.gov/pubmed/16911785
http://dx.doi.org/10.1186/1471-2407-6-207
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