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Pharmacogenomics of endocrine therapy in breast cancer
The most important modality of treatment in the two-thirds of patients with an estrogen receptor (ER)-positive early breast cancer is endocrine therapy. In postmenopausal women, options include the selective ER modulators (SERMs), tamoxifen and raloxifene, and the ‘third-generation’ aromatase inhibi...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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2013
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3926210/ https://www.ncbi.nlm.nih.gov/pubmed/23635953 http://dx.doi.org/10.1038/jhg.2013.35 |
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author | Ingle, James N |
author_facet | Ingle, James N |
author_sort | Ingle, James N |
collection | PubMed |
description | The most important modality of treatment in the two-thirds of patients with an estrogen receptor (ER)-positive early breast cancer is endocrine therapy. In postmenopausal women, options include the selective ER modulators (SERMs), tamoxifen and raloxifene, and the ‘third-generation’ aromatase inhibitors (AIs), anastrozole, exemestane and letrozole. Under the auspices of the National Institutes of Health Global Alliance for Pharmacogenomics, Japan, the Mayo Clinic Pharmacogenomics Research Network Center and the RIKEN Center for Genomic Medicine have worked collaboratively to perform genome-wide association studies (GWAS) in women treated with both SERMs and AIs. On the basis of the results of the GWAS, scientists at the Mayo Clinic have proceeded with functional genomic laboratory studies. As will be seen in this review, this has led to new knowledge relating to endocrine biology that has provided a clear focus for further research to move toward truly personalized medicine for women with breast cancer. |
format | Online Article Text |
id | pubmed-3926210 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
record_format | MEDLINE/PubMed |
spelling | pubmed-39262102014-06-01 Pharmacogenomics of endocrine therapy in breast cancer Ingle, James N J Hum Genet Article The most important modality of treatment in the two-thirds of patients with an estrogen receptor (ER)-positive early breast cancer is endocrine therapy. In postmenopausal women, options include the selective ER modulators (SERMs), tamoxifen and raloxifene, and the ‘third-generation’ aromatase inhibitors (AIs), anastrozole, exemestane and letrozole. Under the auspices of the National Institutes of Health Global Alliance for Pharmacogenomics, Japan, the Mayo Clinic Pharmacogenomics Research Network Center and the RIKEN Center for Genomic Medicine have worked collaboratively to perform genome-wide association studies (GWAS) in women treated with both SERMs and AIs. On the basis of the results of the GWAS, scientists at the Mayo Clinic have proceeded with functional genomic laboratory studies. As will be seen in this review, this has led to new knowledge relating to endocrine biology that has provided a clear focus for further research to move toward truly personalized medicine for women with breast cancer. 2013-05-02 2013-06 /pmc/articles/PMC3926210/ /pubmed/23635953 http://dx.doi.org/10.1038/jhg.2013.35 Text en © 2013 The Japan Society of Human Genetics All rights reserved http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Article Ingle, James N Pharmacogenomics of endocrine therapy in breast cancer |
title | Pharmacogenomics of endocrine therapy in breast cancer |
title_full | Pharmacogenomics of endocrine therapy in breast cancer |
title_fullStr | Pharmacogenomics of endocrine therapy in breast cancer |
title_full_unstemmed | Pharmacogenomics of endocrine therapy in breast cancer |
title_short | Pharmacogenomics of endocrine therapy in breast cancer |
title_sort | pharmacogenomics of endocrine therapy in breast cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3926210/ https://www.ncbi.nlm.nih.gov/pubmed/23635953 http://dx.doi.org/10.1038/jhg.2013.35 |
work_keys_str_mv | AT inglejamesn pharmacogenomicsofendocrinetherapyinbreastcancer |