Oxytocin differentially effects 3β-hydroxysteroid dehydrogenase and α-reductase activities in prostate cancer cell lines

被引:4
|
作者
Assinder, Stephen J.
Davies, Kathryn
Surija, Jonathan
Liu-Fu, Frank
机构
[1] Univ Sydney, Disciplines Physiol, Sch Med Sci, Sydney, NSW 2006, Australia
[2] Univ Sydney, Bosch Inst, Sydney, NSW 2006, Australia
关键词
De novo steroidogenesis; Steroid-5-alpha-reductase; 3-Oxo-5alpha-steroid delta 4-dehydrogenase; Hydroxy-delta-5-steroid dehydrogenase; Progesterone reductase; DE-NOVO STEROIDOGENESIS; INTRATUMORAL ANDROGENS; RECEPTOR SYSTEM; UP-REGULATION; IN-VITRO; CASTRATION; PROLIFERATION; PROGRESSION; EXPRESSION; CARCINOMA;
D O I
10.1016/j.peptides.2015.07.015
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
It is known that oxytocin stimulates steroidogenesis in several organs by modulating activity of 3 beta-hydroxysteroid dehydrogenases (HSD3B) and steroid 5 alpha-reductases (SRD5A). However, this has not been established in prostate cancer where these enzymes, key to local production of androgens, are increased. Analysis of both HSD3B and SRD5A activities using a live cell in situ colourimetric assay demonstrated that in PC-3 cells HSD3B activity was significantly increased by oxytocin whilst SRD5A activity was unchanged. This was confirmed in ELISA based assays of conversion of pregnenolone to progesterone and testosterone to dihydrotestosterone in cell lysates following treatment. In contrast, oxytocin significantly inhibited HSD3B activity in LNCaPs, but significantly increased activity of SRD5A, as confirmed by ELISA assays. Analysis of both cell lines by microarray and qRT-PCR determined that these changes were not due to altered gene transcription. This study demonstrates differential effects of oxytocin on the activities of key de novo steroidogenic enzymes in prostate cancer cells. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:149 / 155
页数:7
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