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Refinement of breast cancer molecular classification by miRNA expression profiles

BACKGROUND: Accurate classification of breast cancer using gene expression profiles has contributed to a better understanding of the biological mechanisms behind the disease and has paved the way for better prognostication and treatment prediction. RESULTS: We found that miRNA profiles largely recap...

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Autores principales: Søkilde, Rolf, Persson, Helena, Ehinger, Anna, Pirona, Anna Chiara, Fernö, Mårten, Hegardt, Cecilia, Larsson, Christer, Loman, Niklas, Malmberg, Martin, Rydén, Lisa, Saal, Lao, Borg, Åke, Vallon-Christerson, Johan, Rovira, Carlos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6580620/
https://www.ncbi.nlm.nih.gov/pubmed/31208318
http://dx.doi.org/10.1186/s12864-019-5887-7
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author Søkilde, Rolf
Persson, Helena
Ehinger, Anna
Pirona, Anna Chiara
Fernö, Mårten
Hegardt, Cecilia
Larsson, Christer
Loman, Niklas
Malmberg, Martin
Rydén, Lisa
Saal, Lao
Borg, Åke
Vallon-Christerson, Johan
Rovira, Carlos
author_facet Søkilde, Rolf
Persson, Helena
Ehinger, Anna
Pirona, Anna Chiara
Fernö, Mårten
Hegardt, Cecilia
Larsson, Christer
Loman, Niklas
Malmberg, Martin
Rydén, Lisa
Saal, Lao
Borg, Åke
Vallon-Christerson, Johan
Rovira, Carlos
author_sort Søkilde, Rolf
collection PubMed
description BACKGROUND: Accurate classification of breast cancer using gene expression profiles has contributed to a better understanding of the biological mechanisms behind the disease and has paved the way for better prognostication and treatment prediction. RESULTS: We found that miRNA profiles largely recapitulate intrinsic subtypes. In the case of HER2-enriched tumors a small set of miRNAs including the HER2-encoded mir-4728 identifies the group with very high specificity. We also identified differential expression of the miR-99a/let-7c/miR-125b miRNA cluster as a marker for separation of the Luminal A and B subtypes. High expression of this miRNA cluster is linked to better overall survival among patients with Luminal A tumors. Correlation between the miRNA cluster and their precursor LINC00478 is highly significant suggesting that its expression could help improve the accuracy of present day’s signatures. CONCLUSIONS: We show here that miRNA expression can be translated into mRNA profiles and that the inclusion of miRNA information facilitates the molecular diagnosis of specific subtypes, in particular the clinically relevant sub-classification of luminal tumors. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-019-5887-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-65806202019-06-24 Refinement of breast cancer molecular classification by miRNA expression profiles Søkilde, Rolf Persson, Helena Ehinger, Anna Pirona, Anna Chiara Fernö, Mårten Hegardt, Cecilia Larsson, Christer Loman, Niklas Malmberg, Martin Rydén, Lisa Saal, Lao Borg, Åke Vallon-Christerson, Johan Rovira, Carlos BMC Genomics Research Article BACKGROUND: Accurate classification of breast cancer using gene expression profiles has contributed to a better understanding of the biological mechanisms behind the disease and has paved the way for better prognostication and treatment prediction. RESULTS: We found that miRNA profiles largely recapitulate intrinsic subtypes. In the case of HER2-enriched tumors a small set of miRNAs including the HER2-encoded mir-4728 identifies the group with very high specificity. We also identified differential expression of the miR-99a/let-7c/miR-125b miRNA cluster as a marker for separation of the Luminal A and B subtypes. High expression of this miRNA cluster is linked to better overall survival among patients with Luminal A tumors. Correlation between the miRNA cluster and their precursor LINC00478 is highly significant suggesting that its expression could help improve the accuracy of present day’s signatures. CONCLUSIONS: We show here that miRNA expression can be translated into mRNA profiles and that the inclusion of miRNA information facilitates the molecular diagnosis of specific subtypes, in particular the clinically relevant sub-classification of luminal tumors. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-019-5887-7) contains supplementary material, which is available to authorized users. BioMed Central 2019-06-17 /pmc/articles/PMC6580620/ /pubmed/31208318 http://dx.doi.org/10.1186/s12864-019-5887-7 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 Article
Søkilde, Rolf
Persson, Helena
Ehinger, Anna
Pirona, Anna Chiara
Fernö, Mårten
Hegardt, Cecilia
Larsson, Christer
Loman, Niklas
Malmberg, Martin
Rydén, Lisa
Saal, Lao
Borg, Åke
Vallon-Christerson, Johan
Rovira, Carlos
Refinement of breast cancer molecular classification by miRNA expression profiles
title Refinement of breast cancer molecular classification by miRNA expression profiles
title_full Refinement of breast cancer molecular classification by miRNA expression profiles
title_fullStr Refinement of breast cancer molecular classification by miRNA expression profiles
title_full_unstemmed Refinement of breast cancer molecular classification by miRNA expression profiles
title_short Refinement of breast cancer molecular classification by miRNA expression profiles
title_sort refinement of breast cancer molecular classification by mirna expression profiles
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6580620/
https://www.ncbi.nlm.nih.gov/pubmed/31208318
http://dx.doi.org/10.1186/s12864-019-5887-7
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