A new dawn for androgens: Novel lessons from 11-oxygenated C19 steroids

被引:110
|
作者
Pretorius, Elzette [1 ]
Ark, Wiebke [2 ]
Storbeck, Karl-Heinz [1 ]
机构
[1] Univ Stellenbosch, Dept Biochem, ZA-7600 Stellenbosch, South Africa
[2] Univ Birmingham, Inst Metab & Syst Res, Birmingham B15 2TT, W Midlands, England
关键词
Adrenal androgens; Castration resistant prostate cancer (CRPC); Congenital adrenal hyperplasia (CAH); Polycystic ovary syndrome (PCOS); 11-Ketotestosterone (11KT); 11-Ketodihydrotestosterone (11KDHT); POLYCYSTIC-OVARY-SYNDROME; CONGENITAL ADRENAL-HYPERPLASIA; RESISTANT PROSTATE-CANCER; 3-BETA-HYDROXYSTEROID DEHYDROGENASE/DELTA(5)-DELTA(4) ISOMERASE; CYTOCHROME B(5) AUGMENTS; 21-HYDROXYLASE DEFICIENCY; HIRSUTE WOMEN; DEHYDROEPIANDROSTERONE-SULFATE; ORAL DEHYDROEPIANDROSTERONE; BETA-HYDROXYANDROSTENEDIONE;
D O I
10.1016/j.mce.2016.08.014
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The abundant adrenal C19 steroid 11 beta-hydroxyandrostenedione (11OA4) has been written off as a dead-end product of adrenal steroidogenesis. However, recent evidence has demonstrated that 11OHA4 is the precursor to the potent androgenic 11-oxygenated steroids, 11-ketotestosterone and 11-ketodihydrotestosterone, that bind and activate the human androgen receptor similarly to testosterone and DHT. The significance of this discovery becomes apparent when considering androgen dependent diseases such as castration resistant prostate cancer and diseases associated with androgen excess, e.g. congenital adrenal hyperplasia and polycystic ovary syndrome. In this review we describe the production and metabolism of 11-oxygenated steroids. We subsequently discuss their androgenic activity and highlight the putative role of these androgens in disease states. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:76 / 85
页数:10
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