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Luminal-B breast cancer and novel therapeutic targets
Gene expression profiling has led to a new molecular classification of breast cancer characterized by four intrinsic subtypes: basal-like, HER2-positive, luminal A, and luminal B. Despite expressing estrogen receptor, the luminal-B subtype confers increased risk of early relapse with endocrine thera...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3326541/ https://www.ncbi.nlm.nih.gov/pubmed/22217398 http://dx.doi.org/10.1186/bcr2904 |
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author | Tran, Ben Bedard, Philippe L |
author_facet | Tran, Ben Bedard, Philippe L |
author_sort | Tran, Ben |
collection | PubMed |
description | Gene expression profiling has led to a new molecular classification of breast cancer characterized by four intrinsic subtypes: basal-like, HER2-positive, luminal A, and luminal B. Despite expressing estrogen receptor, the luminal-B subtype confers increased risk of early relapse with endocrine therapy compared with the luminal-A subtype. Although luminal-B definitions vary, the hallmark appears to be increased expression of proliferation-related genes. Several biological pathways are identified as possible contributors to the poor outcomes, and novel agents targeting these pathways are being developed with aims to improve survival. We review the definition of luminal-B breast cancer, its pathological and clinical features, and potential targets for treatment. |
format | Online Article Text |
id | pubmed-3326541 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-33265412012-05-30 Luminal-B breast cancer and novel therapeutic targets Tran, Ben Bedard, Philippe L Breast Cancer Res Review Gene expression profiling has led to a new molecular classification of breast cancer characterized by four intrinsic subtypes: basal-like, HER2-positive, luminal A, and luminal B. Despite expressing estrogen receptor, the luminal-B subtype confers increased risk of early relapse with endocrine therapy compared with the luminal-A subtype. Although luminal-B definitions vary, the hallmark appears to be increased expression of proliferation-related genes. Several biological pathways are identified as possible contributors to the poor outcomes, and novel agents targeting these pathways are being developed with aims to improve survival. We review the definition of luminal-B breast cancer, its pathological and clinical features, and potential targets for treatment. BioMed Central 2011 2011-11-30 /pmc/articles/PMC3326541/ /pubmed/22217398 http://dx.doi.org/10.1186/bcr2904 Text en Copyright ©2011 BioMed Central Ltd |
spellingShingle | Review Tran, Ben Bedard, Philippe L Luminal-B breast cancer and novel therapeutic targets |
title | Luminal-B breast cancer and novel therapeutic targets |
title_full | Luminal-B breast cancer and novel therapeutic targets |
title_fullStr | Luminal-B breast cancer and novel therapeutic targets |
title_full_unstemmed | Luminal-B breast cancer and novel therapeutic targets |
title_short | Luminal-B breast cancer and novel therapeutic targets |
title_sort | luminal-b breast cancer and novel therapeutic targets |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3326541/ https://www.ncbi.nlm.nih.gov/pubmed/22217398 http://dx.doi.org/10.1186/bcr2904 |
work_keys_str_mv | AT tranben luminalbbreastcancerandnoveltherapeutictargets AT bedardphilippel luminalbbreastcancerandnoveltherapeutictargets |