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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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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. |
format | Online Article Text |
id | pubmed-4506390 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
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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