Trilostane, an inhibitor of 3β-hydroxysteroid dehydrogenase, has an agonistic activity on androgen receptor in human prostate cancer cells.

Abstract:

:The intracellular androgen metabolism and cell activity in prostate cancer cells with mutated (LNCaP-FGC) or wild-type (VCaP) androgen receptors in the presence of trilostane, an inhibitor of 3β-hydroxysteroid dehydrogenase, were examined. Trilostane suppressed the intracellular production of androstenedione, testosterone, and dihydrotestosterone from dehydroepiandrosterone in LNCaP-FGC cells. In both LNCaP-FGC and VCaP cell types, the prostate-specific antigen (PSA) levels in media were increased by trilostane alone in a concentration-dependent manner. Both cells pretreated with trilostane showed a dose-dependent decrease in PSA production with bicalutamide (P<0.001). Trilostane should be used with particular concern when treating prostate cancer.

journal_name

Cancer Lett

journal_title

Cancer letters

authors

Takizawa I,Nishiyama T,Hara N,Hoshii T,Ishizaki F,Miyashiro Y,Takahashi K

doi

10.1016/j.canlet.2010.05.015

subject

Has Abstract

pub_date

2010-11-28 00:00:00

pages

226-30

issue

2

eissn

0304-3835

issn

1872-7980

pii

S0304-3835(10)00304-6

journal_volume

297

pub_type

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