Title: AKR1C3 as a target in castrate resistant prostate cancer.
Authors: Adeniji, Adegoke O; Chen, Mo; Penning, Trevor M
Published In J Steroid Biochem Mol Biol, (2013 Sep)
Abstract: Aberrant androgen receptor (AR) activation is the major driver of castrate resistant prostate cancer (CRPC). CRPC is ultimately fatal and more therapeutic agents are needed to treat this disease. Compounds that target the androgen axis by inhibiting androgen biosynthesis and or AR signaling are potential candidates for use in CRPC treatment and are currently being pursued aggressively. Aldo-keto reductase 1C3 (AKR1C3) plays a pivotal role in androgen biosynthesis within the prostate. It catalyzes the 17-ketoreduction of weak androgen precursors to give testosterone and 5α-dihydrotestosterone. AKR1C3 expression and activity has been implicated in the development of CRPC, making it a rational target. Selective inhibition of AKR1C3 will be important, however, due to the presence of closely related isoforms, AKR1C1 and AKR1C2 that are also involved in androgen inactivation. We examine the evidence that supports the vital role of AKR1C3 in CRPC and recent developments in the discovery of potent and selective AKR1C3 inhibitors. This article is part of a Special Issue entitled 'CSR 2013'.
PubMed ID: 23748150
MeSH Terms: 3-Hydroxysteroid Dehydrogenases/drug effects*; 3-Hydroxysteroid Dehydrogenases/metabolism; Aldo-Keto Reductase Family 1 Member C3; Humans; Hydroxyprostaglandin Dehydrogenases/drug effects*; Hydroxyprostaglandin Dehydrogenases/metabolism; Male; Orchiectomy; Prostatic Neoplasms/metabolism*