Back to Search Start Over

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

Authors :
Antonio Lopez-Beltran
Rodolfo Montironi
Francesco Massari
Elena Verri
Liang Cheng
Roberta Mazzucchelli
Alessia Cimadamore
Matteo Santoni
Gaetano Aurilio
Marina Scarpelli
Aurilio G.
Cimadamore A.
Mazzucchelli R.
Lopez-Beltran A.
Verri E.
Scarpelli M.
Massari F.
Cheng L.
Santoni M.
Montironi R.
Source :
Cells, Vol 9, Iss 2653, p 2653 (2020), Cells 2020, 9(12), 2653, Helvia. Repositorio Institucional de la Universidad de Córdoba, instname, Cells, Helvia: Repositorio Institucional de la Universidad de Córdoba, Universidad de Córdoba
Publication Year :
2020

Abstract

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.

Details

Language :
English
Database :
OpenAIRE
Journal :
Cells, Vol 9, Iss 2653, p 2653 (2020), Cells 2020, 9(12), 2653, Helvia. Repositorio Institucional de la Universidad de Córdoba, instname, Cells, Helvia: Repositorio Institucional de la Universidad de Córdoba, Universidad de Córdoba
Accession number :
edsair.doi.dedup.....c817aaf30e859c25c5ed1f5af5540da0