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miR-30e* is an independent subtype-specific prognostic marker in breast cancer

BACKGROUND: Breast cancer clinical outcome is affected by tumor molecular features, and the identification of subtype-specific prognostic biomarkers is relevant for breast cancer translational research. Gene expression signatures proved to be able to complement prognostic information provided by cla...

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Autores principales: D'Aiuto, F, Callari, M, Dugo, M, Merlino, G, Musella, V, Miodini, P, Paolini, B, Cappelletti, V, Daidone, M G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4506390/
https://www.ncbi.nlm.nih.gov/pubmed/26057454
http://dx.doi.org/10.1038/bjc.2015.206
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author D'Aiuto, F
Callari, M
Dugo, M
Merlino, G
Musella, V
Miodini, P
Paolini, B
Cappelletti, V
Daidone, M G
author_facet D'Aiuto, F
Callari, M
Dugo, M
Merlino, G
Musella, V
Miodini, P
Paolini, B
Cappelletti, V
Daidone, M G
author_sort D'Aiuto, F
collection PubMed
description BACKGROUND: Breast cancer clinical outcome is affected by tumor molecular features, and the identification of subtype-specific prognostic biomarkers is relevant for breast cancer translational research. Gene expression signatures proved to be able to complement prognostic information provided by classical clinico-pathological features. Recently, microRNAs (miRNAs) have been causally linked to tumorigenesis and cancer progression and have been associated with patient outcome, also in breast cancer. METHODS: MicroRNAs associated with the development of distant metastasis were identified in a cohort of 92 ESR1+/ERBB2− lymph node-negative breast cancers from patients not receiving adjuvant treatment. Results were confirmed and further investigated in a total of 1246 miRNA and gene expression profiles of the Molecular Taxonomy of Breast Cancer International Consortium data set. Moderated t-test, univariable and multivariable Cox regression models were used for statistical analyses. RESULTS: miR-30e* was identified as independent protective prognostic factor in lymph node-negative untreated patients with ESR1+/ERBB2− tumours and retained a significant association with a good prognosis in treated patients with the same tumor subtype as well as in the ERBB2+ subtype, but not in ESR1−/ERBB2− tumours. CONCLUSIONS: We highlighted a relevant and subtype-specific role in breast cancer for miR-30e* and demonstrated that adding miRNA markers to gene signatures and clinico-pathological features can help for a better prognostication.
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spelling pubmed-45063902015-07-21 miR-30e* is an independent subtype-specific prognostic marker in breast cancer D'Aiuto, F Callari, M Dugo, M Merlino, G Musella, V Miodini, P Paolini, B Cappelletti, V Daidone, M G Br J Cancer Molecular Diagnostics BACKGROUND: Breast cancer clinical outcome is affected by tumor molecular features, and the identification of subtype-specific prognostic biomarkers is relevant for breast cancer translational research. Gene expression signatures proved to be able to complement prognostic information provided by classical clinico-pathological features. Recently, microRNAs (miRNAs) have been causally linked to tumorigenesis and cancer progression and have been associated with patient outcome, also in breast cancer. METHODS: MicroRNAs associated with the development of distant metastasis were identified in a cohort of 92 ESR1+/ERBB2− lymph node-negative breast cancers from patients not receiving adjuvant treatment. Results were confirmed and further investigated in a total of 1246 miRNA and gene expression profiles of the Molecular Taxonomy of Breast Cancer International Consortium data set. Moderated t-test, univariable and multivariable Cox regression models were used for statistical analyses. RESULTS: miR-30e* was identified as independent protective prognostic factor in lymph node-negative untreated patients with ESR1+/ERBB2− tumours and retained a significant association with a good prognosis in treated patients with the same tumor subtype as well as in the ERBB2+ subtype, but not in ESR1−/ERBB2− tumours. CONCLUSIONS: We highlighted a relevant and subtype-specific role in breast cancer for miR-30e* and demonstrated that adding miRNA markers to gene signatures and clinico-pathological features can help for a better prognostication. Nature Publishing Group 2015-07-14 2015-06-09 /pmc/articles/PMC4506390/ /pubmed/26057454 http://dx.doi.org/10.1038/bjc.2015.206 Text en Copyright © 2015 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under the Creative Commons Attribution-Non-Commercial-Share Alike 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Molecular Diagnostics
D'Aiuto, F
Callari, M
Dugo, M
Merlino, G
Musella, V
Miodini, P
Paolini, B
Cappelletti, V
Daidone, M G
miR-30e* is an independent subtype-specific prognostic marker in breast cancer
title miR-30e* is an independent subtype-specific prognostic marker in breast cancer
title_full miR-30e* is an independent subtype-specific prognostic marker in breast cancer
title_fullStr miR-30e* is an independent subtype-specific prognostic marker in breast cancer
title_full_unstemmed miR-30e* is an independent subtype-specific prognostic marker in breast cancer
title_short miR-30e* is an independent subtype-specific prognostic marker in breast cancer
title_sort mir-30e* is an independent subtype-specific prognostic marker in breast cancer
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4506390/
https://www.ncbi.nlm.nih.gov/pubmed/26057454
http://dx.doi.org/10.1038/bjc.2015.206
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