Androgen receptor function and targeted therapeutics across breast cancer subtypes

被引:50
作者
Kolyvas, Emily A. [1 ,2 ,3 ,4 ]
Caldas, Carlos [1 ,5 ,6 ,7 ]
Kelly, Kathleen [2 ]
Ahmad, Saif S. [1 ,8 ]
机构
[1] Univ Cambridge, Canc Res UK Cambridge Inst, Li Ka Shing Centre, Dept Oncol, Cambridge CB2 0RE, England
[2] NCI, Ctr Canc Res, Lab Genitourinary Canc Pathogenesis, Bethesda, MD USA
[3] Univ Cambridge, Cambridge Inst Med Res, Cambridge Scholars Program, NIH, Cambridge, England
[4] Univ Cambridge, Dept Med, Cambridge Scholars Program, NIH, Cambridge, England
[5] CRUK Cambridge Centre, Breast Canc Programme, Cambridge CB2 0RE, England
[6] Cambridge Univ Hospitals, NIHR, Cambridge BioMed Res Centre, Cambridge Breast Canc Res Unit,NHS Fdn Trust, Cambridge, England
[7] Cambridge Univ Hospitals, NIHR, Cambridge Expt Canc Med Centre, Cambridge Breast Canc Res Unit,NHS Fdn Trust, Cambridge, England
[8] Univ Cambridge, Sch Clin Med, Dept Oncol, Cambridge CB2 0SP, England
关键词
Androgen receptor; Breast cancer; Radiotherapy; DNA damage repair; Androgen deprivation therapy; ADVANCED PROSTATE-CANCER; INVASIVE APOCRINE CARCINOMA; ESTROGEN-RECEPTOR; PROGNOSTIC MARKERS; DNA-REPAIR; IN-SITU; EXPRESSION; TUMOR; RISK; PROLIFERATION;
D O I
10.1186/s13058-022-01574-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Despite significant progress in breast cancer (BC) therapy, it is globally the most commonly diagnosed cancer and leads to the death of over 650,000 women annually. Androgen receptor (AR) is emerging as a potential new therapeutic target in BC. While the role of AR is well established in prostate cancer (PCa), its function in BC remains incompletely understood. Emerging data show that AR's role in BC is dependent on several factors including, but not limited to, disease subtype, tumour microenvironment, and levels of circulating oestrogens and androgens. While targeting AR in PCa is becoming increasingly effective, these advances have yet to make any significant impact on the care of BC patients. However, this approach is increasingly being evaluated in BC and it is clear that improvements in our understanding of AR's role in BC will increase the likelihood of success for AR-targeted therapies. This review summarizes our current understanding of the function of AR across BC subtypes. We highlight limitations in our current knowledge and demonstrate the importance of categorizing BC subtypes effectively, in relation to determining AR activity. Further, we describe the current state of the art regarding AR-targeted approaches for BC as monotherapy or in combination with radiotherapy.
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页数:15
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