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Eur Urol. 2015 Mar;67(3):470-9. doi: 10.1016/j.eururo.2014.09.049. Epub 2014 Oct 8.

Understanding the mechanisms of androgen deprivation resistance in prostate cancer at the molecular level.

Author information

1
Department of Genitourinary Medical Oncology-Research, The University of Texas MD Anderson Cancer Center, Houston, TX, USA. Electronic address: theodoroskarantanosmd@gmail.com.
2
Department of Urology, UC Davis Comprehensive Cancer Center, Sacramento, CA, USA.
3
Cliniques universitaires Saint Luc, Université catholique de Louvain, Brussels, Belgium.
4
Department of Genitourinary Medical Oncology-Research, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
5
Section of Pathological Anatomy, Polytechnic University of the Marche Region, School of Medicine, Ancona, Italy.
6
Brady Urological Institute, Johns Hopkins Medical Institutions, Baltimore, MD, USA.

Abstract

CONTEXT:

Various molecular mechanisms play a role in the development of resistance to androgen deprivation therapy in castration-resistant prostate cancer (CRPC).

OBJECTIVE:

To understand the mechanisms and biological pathways associated with the progression of prostate cancer (PCa) under systemic androgen depletion or administration of the novel antiandrogens abiraterone, enzalutamide, and ARN-509. This review also examines the introduction of novel combinational approaches for patients with CRPC.

EVIDENCE ACQUISITION:

PubMed was the data source. Keywords for the search were castrate resistant prostate cancer, abiraterone, enzalutamide resistance mechanisms, resistance to androgen deprivation, AR mutations, amplifications, splice variants, and AR alterations. Papers published before 1990 were excluded from the review, and only English-language papers were included.

EVIDENCE SYNTHESIS:

This review summarizes the current literature regarding the mechanisms implicated in the development of CRPC and the acquisition of resistance to novel antiandrogen axis agents. The review focuses on androgen biosynthesis in the tumor microenvironment, androgen receptor (AR) alterations and post-transcriptional modifications, the role of glucocorticoid receptor, and alternative oncogenic signaling that is derepressed on maximum AR inhibition and thus promotes cancer survival and progression.

CONCLUSIONS:

The mechanisms implicated in the development of resistance to AR inhibition in PCa are multiple and complex, involving virtually all classes of genomic alteration and leading to a host of selective/adaptive responses. Combinational therapeutic approaches targeting both AR signaling and alternative oncogenic pathways may be reasonable for patients with CRPC.

PATIENT SUMMARY:

We looked for mechanisms related to the progression of PCa in patients undergoing hormonal therapy and treatment with novel drugs targeting the AR. Based on recent data, combining maximal AR inhibition with novel agents targeting other tumor-compensatory, non-AR-related pathways may improve the survival and quality of life of patients with castration-resistant PCa.

KEYWORDS:

Alternative signaling; Androgen receptor; Castration-resistant prostate cancer; Novel antiandrogens

PMID:
25306226
PMCID:
PMC5301306
DOI:
10.1016/j.eururo.2014.09.049
[Indexed for MEDLINE]
Free PMC Article

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