The role of CYP17A1 in prostate cancer development: structure, function, mechanism of action, genetic variations and its inhibition

被引:28
|
作者
Sivonova, Monika Kmet'ova [1 ]
Jurecekova, Jana [1 ]
Tatarkova, Zuzana [1 ]
Kaplan, Peter [1 ]
Lichardusova, Lucia [1 ]
Hatok, Jozef [1 ]
机构
[1] Comenius Univ, Jessenius Fac Med Martin, Dept Med Biochem, Martin, Slovakia
关键词
CYP17A1; Steroid 17 alpha-hydroxylase/17,20-lyase; polymorphisms; inhibitors; Prostate cancer; GENOME-WIDE ASSOCIATION; STEROID 17-ALPHA-HYDROXYLASE/17,20 LYASE; TRANSCRIPTION FACTORS GATA-4; ANDROGEN-RECEPTOR; ANTITUMOR-ACTIVITY; HORMONE-LEVELS; SERINE PHOSPHORYLATION; ADRENOCORTICAL-CELLS; SUSCEPTIBILITY LOCI; PROMOTER VARIANT;
D O I
10.4149/gpb_2017024
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Androgens play an important role during the development of both normal prostate epithelium and prostate cancer and variants of genes involved in androgen metabolism may be related to an increased risk of prostate disease. Cytochrome P450 17 alpha-hydroxylase/17,20-lyase (CYP17A1) is a key regulatory enzyme in the steroidogenic pathway; it catalyses both 17 alpha-hydroxylase and 17,20-lyase activities and is essential for the production of both androgens and glucocorticoids. In this review, we focus on the structure and enzymatic activity of CYP17A1 and the mechanism of modulation of CYP17A1 activities. We discuss the relationship between common genetic variations in CYP17A1 gene and prostate cancer risk and the main effects of these variations on the prediction of susceptibility and clinical outcomes of prostate cancer patients. The mechanism of action, the efficacy and the clinical potential of CYP17A1 inhibitors in prostate cancer are also summarized.
引用
收藏
页码:487 / 499
页数:13
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