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The synthetic androgen mibolerone induces transient suppression of the transformed phenotype in an androgen responsive human prostatic carcinoma cell line.
- Source :
-
Andrologia [Andrologia] 1990; Vol. 22 Suppl 1, pp. 56-66. - Publication Year :
- 1990
-
Abstract
- The synthetic androgen mibolerone elicits a set of distinct changes in the behaviour of an androgen responsive human prostatic carcinoma cell line (LNCaP). Inhibition of cell proliferation, induction of morphological change and of a prostate specific mRNA, and inhibition of colony formation in soft agar are induced by very low concentrations of mibolerone. The natural androgen dihydrotestosterone is much less effective. The changes in growth characteristics and morphology are reverted by excess antiandrogen, i.e. cyproterone acetate or hydroxyflutamide. Cell lines lacking androgen receptors (PC-3, DU 145 and MRC-5) are completely unresponsive to mibolerone. Taken together, our results indicate androgen receptor mediated suppression of the transformed phenotype in LNCaP cells.
- Subjects :
- Androgen Antagonists pharmacology
Cell Division drug effects
Cell Transformation, Neoplastic
Cyproterone analogs & derivatives
Cyproterone pharmacology
Cyproterone Acetate
Dihydrotestosterone pharmacology
Flutamide analogs & derivatives
Flutamide pharmacology
Humans
Male
Nandrolone pharmacology
Prostatic Neoplasms metabolism
RNA, Messenger metabolism
Receptors, Androgen physiology
Tumor Cells, Cultured
Androgens pharmacology
Nandrolone analogs & derivatives
Prostatic Neoplasms pathology
Subjects
Details
- Language :
- English
- ISSN :
- 0303-4569
- Volume :
- 22 Suppl 1
- Database :
- MEDLINE
- Journal :
- Andrologia
- Publication Type :
- Academic Journal
- Accession number :
- 2151880
- Full Text :
- https://doi.org/10.1111/j.1439-0272.1990.tb02071.x