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Combination of MiR-103a-3p and Mesothelin Improves the Biomarker Performance of Malignant Mesothelioma Diagnosis

BACKGROUND: For the detection of malignant mesothelioma no single biomarker with reasonable sensitivity and specificity has been described so far. Mesothelin, the most prominent blood-based biomarker, is characterized by high specificity but low sensitivity. It might be reasonable to combine biomark...

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Autores principales: Weber, Daniel G., Casjens, Swaantje, Johnen, Georg, Bryk, Oleksandr, Raiko, Irina, Pesch, Beate, Kollmeier, Jens, Bauer, Torsten T., Brüning, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4255020/
https://www.ncbi.nlm.nih.gov/pubmed/25469901
http://dx.doi.org/10.1371/journal.pone.0114483
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author Weber, Daniel G.
Casjens, Swaantje
Johnen, Georg
Bryk, Oleksandr
Raiko, Irina
Pesch, Beate
Kollmeier, Jens
Bauer, Torsten T.
Brüning, Thomas
author_facet Weber, Daniel G.
Casjens, Swaantje
Johnen, Georg
Bryk, Oleksandr
Raiko, Irina
Pesch, Beate
Kollmeier, Jens
Bauer, Torsten T.
Brüning, Thomas
author_sort Weber, Daniel G.
collection PubMed
description BACKGROUND: For the detection of malignant mesothelioma no single biomarker with reasonable sensitivity and specificity has been described so far. Mesothelin, the most prominent blood-based biomarker, is characterized by high specificity but low sensitivity. It might be reasonable to combine biomarkers of different molecular classes in order to improve the overall performance. The aim of this study was to assess the performance of the combination of mesothelin and miR-103a-3p as blood-based biomarker for mesothelioma. METHODS/PRINCIPAL FINDINGS: Mesothelin concentration in plasma and miR-103a-3p levels in the cellular blood fraction were analyzed in 43 male mesothelioma patients and 52 male controls formerly exposed to asbestos. For the discrimination of epithelioid and biphasic mesothelioma from asbestos-exposed controls mesothelin and miR-103a-3p showed 74% and 89% sensitivity and 85% and 63% specificity, respectively. For the combination of mesothelin and miR-103a-3p a sensitivity of 95% and a specificity of 81% were calculated. CONCLUSIONS/SIGNIFICANCE: The results of this study show that the combination of mesothelin and miR-103a-3p improves the diagnostic performance of individual blood-based biomarker to detect malignant mesothelioma. The obtained results indicate that the use of biomarkers of different molecular classes might be a reasonable approach to assemble a biomarker panel.
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spelling pubmed-42550202014-12-11 Combination of MiR-103a-3p and Mesothelin Improves the Biomarker Performance of Malignant Mesothelioma Diagnosis Weber, Daniel G. Casjens, Swaantje Johnen, Georg Bryk, Oleksandr Raiko, Irina Pesch, Beate Kollmeier, Jens Bauer, Torsten T. Brüning, Thomas PLoS One Research Article BACKGROUND: For the detection of malignant mesothelioma no single biomarker with reasonable sensitivity and specificity has been described so far. Mesothelin, the most prominent blood-based biomarker, is characterized by high specificity but low sensitivity. It might be reasonable to combine biomarkers of different molecular classes in order to improve the overall performance. The aim of this study was to assess the performance of the combination of mesothelin and miR-103a-3p as blood-based biomarker for mesothelioma. METHODS/PRINCIPAL FINDINGS: Mesothelin concentration in plasma and miR-103a-3p levels in the cellular blood fraction were analyzed in 43 male mesothelioma patients and 52 male controls formerly exposed to asbestos. For the discrimination of epithelioid and biphasic mesothelioma from asbestos-exposed controls mesothelin and miR-103a-3p showed 74% and 89% sensitivity and 85% and 63% specificity, respectively. For the combination of mesothelin and miR-103a-3p a sensitivity of 95% and a specificity of 81% were calculated. CONCLUSIONS/SIGNIFICANCE: The results of this study show that the combination of mesothelin and miR-103a-3p improves the diagnostic performance of individual blood-based biomarker to detect malignant mesothelioma. The obtained results indicate that the use of biomarkers of different molecular classes might be a reasonable approach to assemble a biomarker panel. Public Library of Science 2014-12-03 /pmc/articles/PMC4255020/ /pubmed/25469901 http://dx.doi.org/10.1371/journal.pone.0114483 Text en © 2014 Weber et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Weber, Daniel G.
Casjens, Swaantje
Johnen, Georg
Bryk, Oleksandr
Raiko, Irina
Pesch, Beate
Kollmeier, Jens
Bauer, Torsten T.
Brüning, Thomas
Combination of MiR-103a-3p and Mesothelin Improves the Biomarker Performance of Malignant Mesothelioma Diagnosis
title Combination of MiR-103a-3p and Mesothelin Improves the Biomarker Performance of Malignant Mesothelioma Diagnosis
title_full Combination of MiR-103a-3p and Mesothelin Improves the Biomarker Performance of Malignant Mesothelioma Diagnosis
title_fullStr Combination of MiR-103a-3p and Mesothelin Improves the Biomarker Performance of Malignant Mesothelioma Diagnosis
title_full_unstemmed Combination of MiR-103a-3p and Mesothelin Improves the Biomarker Performance of Malignant Mesothelioma Diagnosis
title_short Combination of MiR-103a-3p and Mesothelin Improves the Biomarker Performance of Malignant Mesothelioma Diagnosis
title_sort combination of mir-103a-3p and mesothelin improves the biomarker performance of malignant mesothelioma diagnosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4255020/
https://www.ncbi.nlm.nih.gov/pubmed/25469901
http://dx.doi.org/10.1371/journal.pone.0114483
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