The roles of aldo-keto reductases in steroid hormone action

被引:65
作者
Bauman, DR [1 ]
Steckelbroeck, S [1 ]
Penning, TM [1 ]
机构
[1] Univ Penn, Sch Med, Dept Pharmacol, Philadelphia, PA 19104 USA
关键词
D O I
10.1358/dnp.2004.17.9.872570
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
dThe human aldo-keto reductase 1 C (AKR1C) isozymes are implicated in the pre-receptor regulation of steroid receptors, nuclear orphan receptors and membrane-bound ligand-gated ion channels. Human AKR members that may regulate the local concentration of steroid hormones include: AKR1C1, AKR1C2, AKR1C3, AKR1C4 and AKR1D1. Since, these enzymes are pluripotent, the physiological role for the human AKR1C isozymes is determined by their tissue-specific expression patterns and their substrate availability in target tissues. AKRs work in concert with short-chain dehydrogenases/reductases as switches to control ligand access to nuclear receptors. Consequently, they are potential targets in treating prostate cancer, breast cancer, endometriosis and endometrial cancer. (C) 2004 Prous Science. All rights reserved.
引用
收藏
页码:563 / 578
页数:16
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