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Estrogen independent gene expression defines clinically relevant subgroups of estrogen receptor positive breast cancer
BACKGROUND: Human breast cancer represents a significantly heterogeneous disease. Global gene expression profiling measurements have been used to classify tumors into multiple molecular subtypes. The capacity to define subtypes of breast tumors provides a framework to enable improved understanding o...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4289221/ https://www.ncbi.nlm.nih.gov/pubmed/25420785 http://dx.doi.org/10.1186/1471-2407-14-871 |
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author | Hallett, Robin M Hassell, John A |
author_facet | Hallett, Robin M Hassell, John A |
author_sort | Hallett, Robin M |
collection | PubMed |
description | BACKGROUND: Human breast cancer represents a significantly heterogeneous disease. Global gene expression profiling measurements have been used to classify tumors into multiple molecular subtypes. The capacity to define subtypes of breast tumors provides a framework to enable improved understanding of the mechanisms of breast oncogenesis, as well as to provide opportunities for improved therapeutic intervention in patients. METHODS: We used publicly available gene expression profiling data to identify ‘estrogen independent’ genes in estrogen receptor alpha (ER+) breast tumors, and subsequently identified 6 subgroups of ER + breast tumors. RESULTS: Each of the 6 identified subgroups exhibited distinct clinical behaviors and biology. Patients whose tumors comprised subgroups 2,5&6 experienced excellent long-term survival, whereas those patients whose tumors belonged to subgroups 1&4 experienced much poorer survival. Breast tumor cell lines representative of the different subgroups responded to therapeutic compounds in accordance with their subgroup classification. CONCLUSIONS: These data support the existence of 6 distinct subgroups of ER + breast cancer and suggest that knowledge of the ER + subgroup status of patient samples have the potential to guide therapy choice. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2407-14-871) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4289221 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42892212015-01-11 Estrogen independent gene expression defines clinically relevant subgroups of estrogen receptor positive breast cancer Hallett, Robin M Hassell, John A BMC Cancer Research Article BACKGROUND: Human breast cancer represents a significantly heterogeneous disease. Global gene expression profiling measurements have been used to classify tumors into multiple molecular subtypes. The capacity to define subtypes of breast tumors provides a framework to enable improved understanding of the mechanisms of breast oncogenesis, as well as to provide opportunities for improved therapeutic intervention in patients. METHODS: We used publicly available gene expression profiling data to identify ‘estrogen independent’ genes in estrogen receptor alpha (ER+) breast tumors, and subsequently identified 6 subgroups of ER + breast tumors. RESULTS: Each of the 6 identified subgroups exhibited distinct clinical behaviors and biology. Patients whose tumors comprised subgroups 2,5&6 experienced excellent long-term survival, whereas those patients whose tumors belonged to subgroups 1&4 experienced much poorer survival. Breast tumor cell lines representative of the different subgroups responded to therapeutic compounds in accordance with their subgroup classification. CONCLUSIONS: These data support the existence of 6 distinct subgroups of ER + breast cancer and suggest that knowledge of the ER + subgroup status of patient samples have the potential to guide therapy choice. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2407-14-871) contains supplementary material, which is available to authorized users. BioMed Central 2014-11-24 /pmc/articles/PMC4289221/ /pubmed/25420785 http://dx.doi.org/10.1186/1471-2407-14-871 Text en © Hallett and Hassell; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Hallett, Robin M Hassell, John A Estrogen independent gene expression defines clinically relevant subgroups of estrogen receptor positive breast cancer |
title | Estrogen independent gene expression defines clinically relevant subgroups of estrogen receptor positive breast cancer |
title_full | Estrogen independent gene expression defines clinically relevant subgroups of estrogen receptor positive breast cancer |
title_fullStr | Estrogen independent gene expression defines clinically relevant subgroups of estrogen receptor positive breast cancer |
title_full_unstemmed | Estrogen independent gene expression defines clinically relevant subgroups of estrogen receptor positive breast cancer |
title_short | Estrogen independent gene expression defines clinically relevant subgroups of estrogen receptor positive breast cancer |
title_sort | estrogen independent gene expression defines clinically relevant subgroups of estrogen receptor positive breast cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4289221/ https://www.ncbi.nlm.nih.gov/pubmed/25420785 http://dx.doi.org/10.1186/1471-2407-14-871 |
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