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Synthetic androgens suppress the transformed phenotype in the human prostate carcinoma cell line LNCaP.

AbstractExperiments have been designed to investigate hormonal effects on the human prostatic carcinoma cell line LNCaP in the presence of complete foetal calf serum. At physiological concentrations (3.3 x 10(-9)M), several derivatives of 17 alpha-methyl-testosterone led to a significant reduction of cell proliferation, inhibition of colony formation in soft agar, change of morphology, induction of a prostate specific mRNA and down-regulation of c-myc RNA. Two different antiandrogens, hydroxyflutamide and cyproterone acetate, were capable of reversing the effects exerted by the synthetic androgens on growth properties. The proliferation rate of control cells devoid of androgen receptor was not inhibited by synthetic androgens. Our results indicate that the cellular androgen response mechanism of LNCaP cells is intact and that synthetic androgens elicit androgen receptor mediated suppression of the transformed phenotype. Rare cases of remission of prostatic cancer on androgen treatment have been reported. LNCaP cells may be a model of an uncommon class of prostatic cancer which responds favourably to androgen treatment.
AuthorsD A Wolf, P Schulz, F Fittler (Affiliation: Institut für Physiologische Chemie, Universität München, Germany.)
JournalBritish journal of cancer (Br J Cancer) Vol. 64 Issue 1 Pg. 47-53 (Jul 1991) ISSN: 0007-0920 ENGLAND
PMID1713053 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antigens, Neoplasm
  • RNA, Messenger
  • Testosterone Congeners
  • Dihydrotestosterone
  • Prostate-Specific Antigen
Topics
  • Antigens, Neoplasm (genetics)
  • Cell Aggregation (drug effects)
  • Cell Division (drug effects)
  • Cell Line
  • Dihydrotestosterone (pharmacology)
  • Genes, myc (drug effects)
  • Humans
  • Male
  • Phenotype
  • Prostate-Specific Antigen
  • Prostatic Neoplasms
  • RNA, Messenger (biosynthesis, genetics)
  • Testosterone Congeners (pharmacology)