共 50 条
Androgen Receptor Signaling Pathway in Prostate Cancer: From Genetics to Clinical Applications
被引:149
|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
来源:
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
相关论文