Pharmacogenomics of endocrine therapy in breast cancer

被引:17
|
作者
Ingle, James N. [1 ]
机构
[1] Mayo Clin, Div Med Oncol, Rochester, MN 55905 USA
关键词
aromatase inhibitors; breast cancer; pharmacogenomics; tamoxifen; SURGICAL ADJUVANT BREAST; STAR P-2 TRIAL; AROMATASE INHIBITORS; OSTEOPOROTIC FRACTURES; POSTMENOPAUSAL WOMEN; BOWEL PROJECT; TAMOXIFEN; METAANALYSIS; OUTCOMES; BONE;
D O I
10.1038/jhg.2013.35
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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.
引用
收藏
页码:306 / 312
页数:7
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