Androgen Receptor Signaling Pathway in Prostate Cancer: From Genetics to Clinical Applications

被引:180
作者
Aurilio, Gaetano [1 ]
Cimadamore, Alessia [2 ]
Mazzucchelli, Roberta [2 ]
Lopez-Beltran, Antonio [3 ]
Verri, Elena [1 ]
Scarpelli, Marina [2 ]
Massari, Francesco [4 ]
Cheng, Liang [5 ]
Santoni, Matteo [6 ]
Montironi, Rodolfo [2 ]
机构
[1] European Inst Oncol IRCCS, Med Oncol Div Urogenital & Head & Neck Tumours, IEO, I-20141 Milan, Italy
[2] Polytech Univ Marche Reg, United Hosp, Sch Med, Sect Pathol Anat, I-60126 Ancona, Italy
[3] Cordoba Univ, Dept Surg, Med Sch, Cordoba 14071, Spain
[4] St Orsola Marcello Malpighi Hosp, Div Oncol, I-40138 Bologna, Italy
[5] Indiana Univ Sch Med, Dept Pathol & Lab Med, Indianapolis, IN 46202 USA
[6] Macerata Hosp, Oncol Unit, I-62100 Macerata, Italy
关键词
prostate cancer; androgen receptor; AR-V7; AR variants; AR antagonists; AR resistance; SPLICE VARIANTS; BINDING DOMAIN; MALIGNANT-TRANSFORMATION; PLASMA DNA; MUTATIONS; HORMONE; ENZALUTAMIDE; RESISTANCE; AR-V7; ABIRATERONE;
D O I
10.3390/cells9122653
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Around 80-90% of prostate cancer (PCa) cases are dependent on androgens at initial diagnosis; hence, androgen ablation therapy directed toward a reduction in serum androgens and the inhibition of androgen receptor (AR) is generally the first therapy adopted. However, the patient's response to androgen ablation therapy is variable, and 20-30% of PCa cases become castration resistant (CRPCa). Several mechanisms can guide treatment resistance to anti-AR molecules. In this regard, AR-dependent and -independent resistance mechanisms can be distinguished within the AR pathway. In this article, we investigate the multitude of AR signaling aspects, encompassing the biological structure of AR, current AR-targeted therapies, mechanisms driving resistance to AR, and AR crosstalk with other pathways, in an attempt to provide a comprehensive review for the PCa research community. We also summarize the new anti-AR drugs approved in non-metastatic castration-resistant PCa, in the castration-sensitive setting, and combination therapies with other drugs.
引用
收藏
页码:1 / 14
页数:14
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