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Are circulating microRNAs suitable for the early detection of malignant mesothelioma? Results from a nested case–control study
OBJECTIVE: Malignant mesothelioma is an aggressive cancer of the serous membranes. For the detection of the tumor at early stages non- or minimally-invasive biomarkers are needed. The circulating biomarkers miR-132-3p, miR-126-3p, and miR-103a-3p were analyzed in a nested case–control study using pl...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6371620/ https://www.ncbi.nlm.nih.gov/pubmed/30744695 http://dx.doi.org/10.1186/s13104-019-4113-7 |
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author | Weber, Daniel Gilbert Brik, Alexander Casjens, Swaantje Burek, Katarzyna Lehnert, Martin Pesch, Beate Taeger, Dirk Brüning, Thomas Johnen, Georg |
author_facet | Weber, Daniel Gilbert Brik, Alexander Casjens, Swaantje Burek, Katarzyna Lehnert, Martin Pesch, Beate Taeger, Dirk Brüning, Thomas Johnen, Georg |
author_sort | Weber, Daniel Gilbert |
collection | PubMed |
description | OBJECTIVE: Malignant mesothelioma is an aggressive cancer of the serous membranes. For the detection of the tumor at early stages non- or minimally-invasive biomarkers are needed. The circulating biomarkers miR-132-3p, miR-126-3p, and miR-103a-3p were analyzed in a nested case–control study using plasma samples from 17 prediagnostic mesothelioma cases and 34 matched asbestos-exposed controls without a malignant disease. RESULTS: Using prediagnostic plasma samples collected in median 8.9 months prior the clinical diagnosis miR-132-3p, miR-126-3p, and miR-103a-3p revealed 0% sensitivity on a defined specificity of 98%. Thus, the analyzed miRNAs failed to detect the cancer in prediagnostic samples, showing that they are not feasible for the early detection of malignant mesothelioma. However, the miRNAs might still serve as possible markers for prognosis and response to therapy, but this needs to be analyzed in appropriate studies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13104-019-4113-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6371620 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63716202019-02-25 Are circulating microRNAs suitable for the early detection of malignant mesothelioma? Results from a nested case–control study Weber, Daniel Gilbert Brik, Alexander Casjens, Swaantje Burek, Katarzyna Lehnert, Martin Pesch, Beate Taeger, Dirk Brüning, Thomas Johnen, Georg BMC Res Notes Research Note OBJECTIVE: Malignant mesothelioma is an aggressive cancer of the serous membranes. For the detection of the tumor at early stages non- or minimally-invasive biomarkers are needed. The circulating biomarkers miR-132-3p, miR-126-3p, and miR-103a-3p were analyzed in a nested case–control study using plasma samples from 17 prediagnostic mesothelioma cases and 34 matched asbestos-exposed controls without a malignant disease. RESULTS: Using prediagnostic plasma samples collected in median 8.9 months prior the clinical diagnosis miR-132-3p, miR-126-3p, and miR-103a-3p revealed 0% sensitivity on a defined specificity of 98%. Thus, the analyzed miRNAs failed to detect the cancer in prediagnostic samples, showing that they are not feasible for the early detection of malignant mesothelioma. However, the miRNAs might still serve as possible markers for prognosis and response to therapy, but this needs to be analyzed in appropriate studies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13104-019-4113-7) contains supplementary material, which is available to authorized users. BioMed Central 2019-02-11 /pmc/articles/PMC6371620/ /pubmed/30744695 http://dx.doi.org/10.1186/s13104-019-4113-7 Text en © The Author(s) 2019 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 Note Weber, Daniel Gilbert Brik, Alexander Casjens, Swaantje Burek, Katarzyna Lehnert, Martin Pesch, Beate Taeger, Dirk Brüning, Thomas Johnen, Georg Are circulating microRNAs suitable for the early detection of malignant mesothelioma? Results from a nested case–control study |
title | Are circulating microRNAs suitable for the early detection of malignant mesothelioma? Results from a nested case–control study |
title_full | Are circulating microRNAs suitable for the early detection of malignant mesothelioma? Results from a nested case–control study |
title_fullStr | Are circulating microRNAs suitable for the early detection of malignant mesothelioma? Results from a nested case–control study |
title_full_unstemmed | Are circulating microRNAs suitable for the early detection of malignant mesothelioma? Results from a nested case–control study |
title_short | Are circulating microRNAs suitable for the early detection of malignant mesothelioma? Results from a nested case–control study |
title_sort | are circulating micrornas suitable for the early detection of malignant mesothelioma? results from a nested case–control study |
topic | Research Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6371620/ https://www.ncbi.nlm.nih.gov/pubmed/30744695 http://dx.doi.org/10.1186/s13104-019-4113-7 |
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