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Molecular Classification of Triple-Negative Breast Cancer
Tumor heterogeneity of triple-negative breast cancer (TNBC) has been the main barrier in conquering breast cancer. To dissect the molecular diversity of TNBC and discover therapeutic targets for TNBC, the molecular classification of TNBC is a prioritized issue in research area. Accordingly, recent s...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Breast Cancer Society
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5053306/ https://www.ncbi.nlm.nih.gov/pubmed/27721871 http://dx.doi.org/10.4048/jbc.2016.19.3.223 |
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author | Ahn, Sung Gwe Kim, Seung Jun Kim, Cheungyeul Jeong, Joon |
author_facet | Ahn, Sung Gwe Kim, Seung Jun Kim, Cheungyeul Jeong, Joon |
author_sort | Ahn, Sung Gwe |
collection | PubMed |
description | Tumor heterogeneity of triple-negative breast cancer (TNBC) has been the main barrier in conquering breast cancer. To dissect the molecular diversity of TNBC and discover therapeutic targets for TNBC, the molecular classification of TNBC is a prioritized issue in research area. Accordingly, recent studies have been successful in classifying TNBC into several distinct subtypes with specific biologic pathways. Despite the different methodologies used and varied number of final subtypes, these studies identically suggested that TNBC consists of four major subtypes: basal-like, mesenchymal, luminal androgen receptor, and immune-enriched. By reviewing these methods of classifications of TNBC, we highlight the unmet need to develop a molecular classifier suited for TNBC. |
format | Online Article Text |
id | pubmed-5053306 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Korean Breast Cancer Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-50533062016-10-07 Molecular Classification of Triple-Negative Breast Cancer Ahn, Sung Gwe Kim, Seung Jun Kim, Cheungyeul Jeong, Joon J Breast Cancer Review Article Tumor heterogeneity of triple-negative breast cancer (TNBC) has been the main barrier in conquering breast cancer. To dissect the molecular diversity of TNBC and discover therapeutic targets for TNBC, the molecular classification of TNBC is a prioritized issue in research area. Accordingly, recent studies have been successful in classifying TNBC into several distinct subtypes with specific biologic pathways. Despite the different methodologies used and varied number of final subtypes, these studies identically suggested that TNBC consists of four major subtypes: basal-like, mesenchymal, luminal androgen receptor, and immune-enriched. By reviewing these methods of classifications of TNBC, we highlight the unmet need to develop a molecular classifier suited for TNBC. Korean Breast Cancer Society 2016-09 2016-09-23 /pmc/articles/PMC5053306/ /pubmed/27721871 http://dx.doi.org/10.4048/jbc.2016.19.3.223 Text en © 2016 Korean Breast Cancer Society. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Ahn, Sung Gwe Kim, Seung Jun Kim, Cheungyeul Jeong, Joon Molecular Classification of Triple-Negative Breast Cancer |
title | Molecular Classification of Triple-Negative Breast Cancer |
title_full | Molecular Classification of Triple-Negative Breast Cancer |
title_fullStr | Molecular Classification of Triple-Negative Breast Cancer |
title_full_unstemmed | Molecular Classification of Triple-Negative Breast Cancer |
title_short | Molecular Classification of Triple-Negative Breast Cancer |
title_sort | molecular classification of triple-negative breast cancer |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5053306/ https://www.ncbi.nlm.nih.gov/pubmed/27721871 http://dx.doi.org/10.4048/jbc.2016.19.3.223 |
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