Targeting the Androgen Receptor in Breast Cancer

被引:84
作者
Chia, KeeMing [1 ]
O'Brien, Megan [1 ,4 ]
Brown, Myles [5 ]
Lim, Elgene [1 ,2 ,3 ,4 ,5 ]
机构
[1] Olivia Newton John Canc Res Inst, Heidelberg, Vic, Australia
[2] Univ Melbourne, Melbourne, Vic, Australia
[3] La Trobe Univ, Bundoora, Vic, Australia
[4] Dana Farber Canc Inst, Boston, MA 02115 USA
[5] Harvard Univ, Boston, MA 02115 USA
基金
英国医学研究理事会;
关键词
Androgen receptor; Breast cancer; Breast cancer subtype; Androgen receptor-directed therapy; TAMOXIFEN RESISTANCE; PIK3CA MUTATIONS; PHASE-II; ER-ALPHA; EXPRESSION; THERAPY; BETA; ENDOCRINE; TUMORS; IDENTIFICATION;
D O I
10.1007/s11912-014-0427-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The androgen receptor (AR) is expressed in the majority of breast cancer and across the three main breast cancer subtypes. Historically, the oncogenic role of AR has best been described in molecular apocrine breast cancers, an estrogen receptor (ER)-/AR+ subtype which has a steroid response signature similar to that in the ER-positive breast cancer. The signalling effect of AR is likely to be different across breast cancer subtypes, and particularly important is its interaction with ER signalling. Despite the high frequency of AR expression in breast cancer, it is still not a standard clinical practice to use AR antagonists as therapy. Older trials of AR-directed therapies in breast cancer have had generally been disappointing. More recently, more potent, next-generation, AR-directed therapies have been developed in the context of prostate cancer. Here, we will review the emerging literature dissecting the role of AR signalling in a context-dependent manner in breast cancer and the renewed interest and wave of clinical trials targeting the AR in breast cancer.
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页数:6
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