Trilostane, an inhibitor of 3β-hydroxysteroid dehydrogenase, has an agonistic activity on androgen receptor in human prostate cancer cells.
@article{Takizawa2010TrilostaneAI, title={Trilostane, an inhibitor of 3β-hydroxysteroid dehydrogenase, has an agonistic activity on androgen receptor in human prostate cancer cells.}, author={I. Takizawa and T. Nishiyama and N. Hara and T. Hoshii and F. Ishizaki and Y. Miyashiro and K. Takahashi}, journal={Cancer letters}, year={2010}, volume={297 2}, pages={ 226-30 } }
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… CONTINUE READING
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References
SHOWING 1-10 OF 29 REFERENCES
Inhibition of 3β-hydroxysteroid-dehydrogenase : an approach for prostate cancer treatment ?
- Biology
- 1995
- 16
Primary aldosteronism treated by trilostane (3 beta-hydroxysteroid dehydrogenase inhibitor).
- Medicine
- Urology
- 1985
- 14
Trilostane in advanced breast cancer
- Medicine
- Expert opinion on pharmacotherapy
- 2006
- 10
- Highly Influential
Comparison of effects of 4-hydroxy tamoxifen and trilostane on oestrogen-regulated gene expression in MCF-7 cells: Up-regulation of oestrogen receptor beta
- Biology, Medicine
- The Journal of Steroid Biochemistry and Molecular Biology
- 2006
- 10
Science behind total androgen blockade: from gene to combination therapy.
- Medicine
- Clinical and investigative medicine. Medecine clinique et experimentale
- 1993
- 103
Non‐competitive steroid inhibition of oestrogen receptor functions
- Biology, Medicine
- International journal of cancer
- 2002
- 35
Role of 17β-Hydroxysteroid Dehydrogenases in Sex Steroid Formation in Peripheral Intracrine Tissues
- Biology, Medicine
- Trends in Endocrinology & Metabolism
- 2000
- 139
Intracrinology of estrogens and androgens in breast carcinoma
- Biology, Medicine
- The Journal of Steroid Biochemistry and Molecular Biology
- 2008
- 77
A mutation in the ligand binding domain of the androgen receptor of human LNCaP cells affects steroid binding characteristics and response to anti-androgens.
- Biology, Medicine
- Biochemical and biophysical research communications
- 1990
- 940
- PDF