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
相关论文
共 89 条
[51]  
Linja MJ, 2001, CANCER RES, V61, P3550
[52]   AR Variant ARv567es Induces Carcinogenesis in a Novel Transgenic Mouse Model of Prostate Cancer [J].
Liu, Gang ;
Sprenger, Cynthia ;
Sun, Shihua ;
Epilepsia, Kathryn Soriano ;
Haugk, Kathleen ;
Zhang, Xiaotun ;
Coleman, Ilsa ;
Nelson, Peter S. ;
Plymate, Stephen .
NEOPLASIA, 2013, 15 (09) :1009-1017
[53]   A Whole Blood Assay for AR-V7 and ARv567es in Patients with Prostate Cancer [J].
Liu, Xichun ;
Ledet, Elisa ;
Li, Dongying ;
Dotiwala, Ary ;
Steinberger, Allie ;
Feibus, Allison ;
Li, Jianzhuo ;
Qi, Yanfeng ;
Silberstein, Jonathan ;
Lee, Benjamin ;
Dong, Yan ;
Sartor, Oliver ;
Zhang, Haitao .
JOURNAL OF UROLOGY, 2016, 196 (06) :1758-1763
[54]  
Lotan TL, 2020, AM J SURG PATHOL, V44, pE15, DOI 10.1097/PAS.0000000000001450
[55]   Decoding the androgen receptor splice variants [J].
Lu, Changxue ;
Luo, Jun .
TRANSLATIONAL ANDROLOGY AND UROLOGY, 2013, 2 (03) :178-186
[56]   Development of AR-V7 as a putative treatment selection marker for metastatic castration-resistant prostate cancer [J].
Luo, Jun .
ASIAN JOURNAL OF ANDROLOGY, 2016, 18 (04) :580-585
[57]   The Androgen Receptor in Health and Disease [J].
Matsumoto, Takahiro ;
Sakari, Matomo ;
Okada, Maiko ;
Yokoyama, Atsushi ;
Takahashi, Sayuri ;
Kouzmenko, Alexander ;
Kato, Shigeaki .
ANNUAL REVIEW OF PHYSIOLOGY, VOL 75, 2013, 75 :201-224
[58]   A review on the interactions between the tumor microenvironment and androgen receptor signaling in prostate cancer [J].
McAllister, Milly J. ;
Underwood, Mark A. ;
Leung, Hing Y. ;
Edwards, Joanne .
TRANSLATIONAL RESEARCH, 2019, 206 :91-106
[59]   Δ5-androstenediol is a natural hormone with androgenic activity in human prostate cancer cells [J].
Miyamoto, H ;
Yeh, SY ;
Lardy, H ;
Messing, E ;
Chang, CS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (19) :11083-11088
[60]  
Mononen N, 2000, CANCER RES, V60, P6479