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Evaluation of long noncoding RNA MALAT1 as a candidate blood-based biomarker for the diagnosis of non-small cell lung cancer

BACKGROUND: The long noncoding RNA MALAT1 (metastasis-associated lung adenocarcinoma transcript 1) is described as a potential biomarker for NSCLC (non-small cell lung cancer). Diagnostic biomarkers need to be detectable in easily accessible body fluids, should be characterized by high specificity,...

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Autores principales: Weber, Daniel Gilbert, Johnen, Georg, Casjens, Swaantje, Bryk, Oleksandr, Pesch, Beate, Jöckel, Karl-Heinz, Kollmeier, Jens, Brüning, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4029199/
https://www.ncbi.nlm.nih.gov/pubmed/24313945
http://dx.doi.org/10.1186/1756-0500-6-518
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author Weber, Daniel Gilbert
Johnen, Georg
Casjens, Swaantje
Bryk, Oleksandr
Pesch, Beate
Jöckel, Karl-Heinz
Kollmeier, Jens
Brüning, Thomas
author_facet Weber, Daniel Gilbert
Johnen, Georg
Casjens, Swaantje
Bryk, Oleksandr
Pesch, Beate
Jöckel, Karl-Heinz
Kollmeier, Jens
Brüning, Thomas
author_sort Weber, Daniel Gilbert
collection PubMed
description BACKGROUND: The long noncoding RNA MALAT1 (metastasis-associated lung adenocarcinoma transcript 1) is described as a potential biomarker for NSCLC (non-small cell lung cancer). Diagnostic biomarkers need to be detectable in easily accessible body fluids, should be characterized by high specificity, sufficient sensitivity, and robustness against influencing factors. The aim of this study was to evaluate the performance of MALAT1 as a blood based biomarker for NSCLC. RESULTS: MALAT1 was shown to be detectable in the cellular fraction of peripheral human blood, showing different expression levels between cancer patients and cancer-free controls. For the discrimination of NSCLC patients from cancer-free controls a sensitivity of 56% was calculated conditional on a high specificity of 96%. No impact of tumor stage, age, gender, and smoking status on MALAT1 levels could be observed, but results based on small numbers. CONCLUSIONS: The results of this study indicate that MALAT1 complies with key characteristics of diagnostic biomarkers, i.e., minimal invasiveness, high specificity, and robustness. Due to its relatively low sensitivity MALAT1 might not be feasible as a single biomarker for the diagnosis of NSCLC in the cellular fraction of blood. Alternatively, MALAT1 might be applicable as a complementary biomarker within a panel in order to improve the entire diagnostic performance.
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spelling pubmed-40291992014-05-22 Evaluation of long noncoding RNA MALAT1 as a candidate blood-based biomarker for the diagnosis of non-small cell lung cancer Weber, Daniel Gilbert Johnen, Georg Casjens, Swaantje Bryk, Oleksandr Pesch, Beate Jöckel, Karl-Heinz Kollmeier, Jens Brüning, Thomas BMC Res Notes Research Article BACKGROUND: The long noncoding RNA MALAT1 (metastasis-associated lung adenocarcinoma transcript 1) is described as a potential biomarker for NSCLC (non-small cell lung cancer). Diagnostic biomarkers need to be detectable in easily accessible body fluids, should be characterized by high specificity, sufficient sensitivity, and robustness against influencing factors. The aim of this study was to evaluate the performance of MALAT1 as a blood based biomarker for NSCLC. RESULTS: MALAT1 was shown to be detectable in the cellular fraction of peripheral human blood, showing different expression levels between cancer patients and cancer-free controls. For the discrimination of NSCLC patients from cancer-free controls a sensitivity of 56% was calculated conditional on a high specificity of 96%. No impact of tumor stage, age, gender, and smoking status on MALAT1 levels could be observed, but results based on small numbers. CONCLUSIONS: The results of this study indicate that MALAT1 complies with key characteristics of diagnostic biomarkers, i.e., minimal invasiveness, high specificity, and robustness. Due to its relatively low sensitivity MALAT1 might not be feasible as a single biomarker for the diagnosis of NSCLC in the cellular fraction of blood. Alternatively, MALAT1 might be applicable as a complementary biomarker within a panel in order to improve the entire diagnostic performance. BioMed Central 2013-12-06 /pmc/articles/PMC4029199/ /pubmed/24313945 http://dx.doi.org/10.1186/1756-0500-6-518 Text en Copyright © 2013 Weber 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
Weber, Daniel Gilbert
Johnen, Georg
Casjens, Swaantje
Bryk, Oleksandr
Pesch, Beate
Jöckel, Karl-Heinz
Kollmeier, Jens
Brüning, Thomas
Evaluation of long noncoding RNA MALAT1 as a candidate blood-based biomarker for the diagnosis of non-small cell lung cancer
title Evaluation of long noncoding RNA MALAT1 as a candidate blood-based biomarker for the diagnosis of non-small cell lung cancer
title_full Evaluation of long noncoding RNA MALAT1 as a candidate blood-based biomarker for the diagnosis of non-small cell lung cancer
title_fullStr Evaluation of long noncoding RNA MALAT1 as a candidate blood-based biomarker for the diagnosis of non-small cell lung cancer
title_full_unstemmed Evaluation of long noncoding RNA MALAT1 as a candidate blood-based biomarker for the diagnosis of non-small cell lung cancer
title_short Evaluation of long noncoding RNA MALAT1 as a candidate blood-based biomarker for the diagnosis of non-small cell lung cancer
title_sort evaluation of long noncoding rna malat1 as a candidate blood-based biomarker for the diagnosis of non-small cell lung cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4029199/
https://www.ncbi.nlm.nih.gov/pubmed/24313945
http://dx.doi.org/10.1186/1756-0500-6-518
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