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Calretinin as a blood-based biomarker for mesothelioma

BACKGROUND: Malignant mesothelioma (MM) is a deadly cancer mainly caused by previous exposure to asbestos. With a latency period up to 50 years the incidence of MM is still increasing, even in countries that banned asbestos. Secondary prevention has been established to provide persons at risk regula...

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Autores principales: Johnen, Georg, Gawrych, Katarzyna, Raiko, Irina, Casjens, Swaantje, Pesch, Beate, Weber, Daniel G., Taeger, Dirk, Lehnert, Martin, Kollmeier, Jens, Bauer, Torsten, Musk, Arthur W., Robinson, Bruce W. S., Brüning, Thomas, Creaney, Jenette
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5450182/
https://www.ncbi.nlm.nih.gov/pubmed/28558669
http://dx.doi.org/10.1186/s12885-017-3375-5
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author Johnen, Georg
Gawrych, Katarzyna
Raiko, Irina
Casjens, Swaantje
Pesch, Beate
Weber, Daniel G.
Taeger, Dirk
Lehnert, Martin
Kollmeier, Jens
Bauer, Torsten
Musk, Arthur W.
Robinson, Bruce W. S.
Brüning, Thomas
Creaney, Jenette
author_facet Johnen, Georg
Gawrych, Katarzyna
Raiko, Irina
Casjens, Swaantje
Pesch, Beate
Weber, Daniel G.
Taeger, Dirk
Lehnert, Martin
Kollmeier, Jens
Bauer, Torsten
Musk, Arthur W.
Robinson, Bruce W. S.
Brüning, Thomas
Creaney, Jenette
author_sort Johnen, Georg
collection PubMed
description BACKGROUND: Malignant mesothelioma (MM) is a deadly cancer mainly caused by previous exposure to asbestos. With a latency period up to 50 years the incidence of MM is still increasing, even in countries that banned asbestos. Secondary prevention has been established to provide persons at risk regular health examinations. An earlier detection with tumor markers might improve therapeutic options. Previously, we have developed a new blood-based assay for the protein marker calretinin. Aim of this study was the verification of the assay in an independent study population and comparison with the established marker mesothelin. METHODS: For a case-control study in men, a total of 163 cases of pleural MM and 163 controls were available from Australia, another 36 cases and 72 controls were recruited in Germany. All controls had asbestosis and/or plaques. Calretinin and mesothelin were determined by ELISA (enzyme-linked immunosorbent assay) in serum or plasma collected prior to therapy. We estimated the performance of both markers and tested factors potentially influencing marker concentrations like age, sample storage time, and MM subtype. RESULTS: Calretinin was able to detect all major subtypes except for sarcomatoid MM. Calretinin showed a similar performance in Australian and German men. At a pre-defined specificity of 95% the sensitivity of calretinin reached 71% and that of mesothelin 69%, when excluding sarcomatoid MM. At 97% specificity, the combination with calretinin increased the sensitivity of mesothelin from 66% to 75%. Sample storage time did not influence the results. In controls the concentrations of calretinin increased 1.87-fold (95% CI 1.10–3.20) per 10 years of age and slightly more for mesothelin (2.28, 95% CI 1.30–4.00). CONCLUSIONS: Calretinin could be verified as a blood-based marker for MM. The assay is robust and shows a performance that is comparable to that of mesothelin. Retrospective analyses would not be limited by storage time. The high specificity supports a combination of calretinin with other markers. Calretinin is specific for epithelioid and biphasic MM but not the rarer sarcomatoid form. Molecular markers like calretinin and mesothelin are promising tools to improve and supplement the diagnosis of MM and warrant further validation in a prospective study. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12885-017-3375-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-54501822017-06-01 Calretinin as a blood-based biomarker for mesothelioma Johnen, Georg Gawrych, Katarzyna Raiko, Irina Casjens, Swaantje Pesch, Beate Weber, Daniel G. Taeger, Dirk Lehnert, Martin Kollmeier, Jens Bauer, Torsten Musk, Arthur W. Robinson, Bruce W. S. Brüning, Thomas Creaney, Jenette BMC Cancer Research Article BACKGROUND: Malignant mesothelioma (MM) is a deadly cancer mainly caused by previous exposure to asbestos. With a latency period up to 50 years the incidence of MM is still increasing, even in countries that banned asbestos. Secondary prevention has been established to provide persons at risk regular health examinations. An earlier detection with tumor markers might improve therapeutic options. Previously, we have developed a new blood-based assay for the protein marker calretinin. Aim of this study was the verification of the assay in an independent study population and comparison with the established marker mesothelin. METHODS: For a case-control study in men, a total of 163 cases of pleural MM and 163 controls were available from Australia, another 36 cases and 72 controls were recruited in Germany. All controls had asbestosis and/or plaques. Calretinin and mesothelin were determined by ELISA (enzyme-linked immunosorbent assay) in serum or plasma collected prior to therapy. We estimated the performance of both markers and tested factors potentially influencing marker concentrations like age, sample storage time, and MM subtype. RESULTS: Calretinin was able to detect all major subtypes except for sarcomatoid MM. Calretinin showed a similar performance in Australian and German men. At a pre-defined specificity of 95% the sensitivity of calretinin reached 71% and that of mesothelin 69%, when excluding sarcomatoid MM. At 97% specificity, the combination with calretinin increased the sensitivity of mesothelin from 66% to 75%. Sample storage time did not influence the results. In controls the concentrations of calretinin increased 1.87-fold (95% CI 1.10–3.20) per 10 years of age and slightly more for mesothelin (2.28, 95% CI 1.30–4.00). CONCLUSIONS: Calretinin could be verified as a blood-based marker for MM. The assay is robust and shows a performance that is comparable to that of mesothelin. Retrospective analyses would not be limited by storage time. The high specificity supports a combination of calretinin with other markers. Calretinin is specific for epithelioid and biphasic MM but not the rarer sarcomatoid form. Molecular markers like calretinin and mesothelin are promising tools to improve and supplement the diagnosis of MM and warrant further validation in a prospective study. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12885-017-3375-5) contains supplementary material, which is available to authorized users. BioMed Central 2017-05-30 /pmc/articles/PMC5450182/ /pubmed/28558669 http://dx.doi.org/10.1186/s12885-017-3375-5 Text en © The Author(s). 2017 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 Research Article
Johnen, Georg
Gawrych, Katarzyna
Raiko, Irina
Casjens, Swaantje
Pesch, Beate
Weber, Daniel G.
Taeger, Dirk
Lehnert, Martin
Kollmeier, Jens
Bauer, Torsten
Musk, Arthur W.
Robinson, Bruce W. S.
Brüning, Thomas
Creaney, Jenette
Calretinin as a blood-based biomarker for mesothelioma
title Calretinin as a blood-based biomarker for mesothelioma
title_full Calretinin as a blood-based biomarker for mesothelioma
title_fullStr Calretinin as a blood-based biomarker for mesothelioma
title_full_unstemmed Calretinin as a blood-based biomarker for mesothelioma
title_short Calretinin as a blood-based biomarker for mesothelioma
title_sort calretinin as a blood-based biomarker for mesothelioma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5450182/
https://www.ncbi.nlm.nih.gov/pubmed/28558669
http://dx.doi.org/10.1186/s12885-017-3375-5
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