Androgen receptor in estrogen receptor positive breast cancer: Beyond expression |
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Affiliation: | 1. Department of Oncology, the People''s Hospital of Yuxi City, Yuxi 653100, China;2. Department of Cardiothoracic Surgery, Southwest Hospital, Third Military Medical University, Chongqing 400038, China;3. College of Bioengineering, Chongqing University, Chongqing 400044, China;1. Department of Biochemistry and Molecular Biology, Wayne State University School of Medicine, Detroit, MI 48201, USA;2. Department of Biochemistry and Molecular Biology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA;3. Center for Cancer Epigenetics, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA;4. Advanced Photon Source, Argonne National Laboratory, Argonne, IL 60439, USA;5. Nutraceuticals and Functional Food Research and Development Center, Faculty of Agro-Industry, Prince of Songkla University, Hat-Yai, Songkhla 90112, Thailand |
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Abstract: | In recent years, new therapeutic approaches have reshaped the overall strategy of breast cancer (BC) treatment and have markedly improved patient survival. This is, in part, due to novel therapies for estrogen receptor (ER)-positive BC. Unfortunately, many patients present de novo resistance to these therapies or develop an acquired resistance over time. Therefore, research is now focused on discovering new molecular targets to overcome these resistances. Interestingly, preclinical and clinical studies have shown a critical role for the cross-talk between androgen receptor (AR) and ER in luminal-like BC. AR is expressed in >60% of BC and in up to 90% of ERα-positive tumors. Multiple studies suggest that AR is associated with a favorable prognosis. However, AR overexpression and, in particular, the high AR:ER ratio, seem to be involved in resistance to hormonal treatment. In this setting, a group of BCs could benefit from AR-inhibitors; nevertheless, some ER-positive BC patients do not seem to benefit from this strategy. Therefore, it is crucial to identify biomarkers that would enable the selection of patients who might benefit from combination treatment with ER and AR inhibitors. |
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Keywords: | Breast cancer Androgen receptor Anti-androgen therapy Endocrine resistance |
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