Regulatory genes in the androgen production, uptake and conversion (APUC) pathway in advanced prostate cancer

Author:

McSweeney Sean1ORCID,Bergom Hannah E23,Prizment Anna23,Halabi Susan4,Sharifi Nima5ORCID,Ryan Charles126,Hwang Justin23ORCID

Affiliation:

1. University of Minnesota Medical School, Minneapolis, Minnesota, USA

2. Department of Medicine, University of Minnesota Masonic Cancer Center, Minneapolis, Minnesota, USA

3. Division of Hematology, Oncology and Transplantation, University of Minnesota, Minneapolis, Minnesota, USA

4. Department of Biostatistics and Bioinformatics, Duke University, Durham, North Carolina, USA

5. Genitourinary Malignancies Research Center, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio, USA

6. Prostate Cancer Foundation, Santa Monica, California, USA

Abstract

The androgen receptor (AR) signaling pathway regulates the progression of prostate cancer (PC). Metastatic castration-resistant prostate cancer (mCRPC) patients generally receive AR-targeted therapies (ART) or androgen-deprivation therapies (ADT) with the initial response; however, resistance is inevitably observed. Prior studies have shown activity and upregulation of a family of androgen production, uptake, and conversion – APUC genes – based on genomic analyses of patient germlines. Genetic variants of some APUC genes, such as the conversion gene, HSD3B1, predict response to second-generation androgen-targeted therapies. Studies have begun to elucidate the overall role of APUC genes, each with unique actionable enzymatic activity, in mCRPC patient outcomes. The current role and knowledge of the genetic and genomic features of APUC genes in advanced prostate cancer and beyond are discussed in this review. These studies inform of how interpreting behavior of APUC genes through genomic tools will impact the treatment of advanced prostate cancer.

Publisher

Bioscientifica

Subject

General Engineering

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