Androgen regulation of ornithine decarboxylase in human prostatic cells identified using differential display

Alan M. Betts, Ian Waite, David E. Neal, Craig N. Robson

Research output: Contribution to journalArticlepeer-review

33 Scopus citations

Abstract

Androgens are essential for normal prostate physiology and have a permissive role in the development and progression of prostate cancer. Using the mRNA differential display technique, ornithine decarboxylase (ODC) was identified to be up-regulated by androgens in human prostatic LNCaP cells. On Northern analysis, the induction of ODC expression by 10 nM androgen was rapid and continued up to 48 h exposure with a maximum 6.3-fold up-regulation. The anti-androgen Casodex inhibited the androgen-induced up-regulation of DC, whereas the protein synthesis inhibitor cycloheximide did not. Together these data suggest that regulation is mediated through the androgen receptor protein and does require secondary protein synthesis, respectively. The kinetics of induction of ODC were almost identical to those of prostate specific antigen. Taken together these data suggest that ODC is directly regulated by androgens in LNCaP cells.

Original languageEnglish
Pages (from-to)328-332
Number of pages5
JournalFEBS Letters
Volume405
Issue number3
DOIs
StatePublished - Apr 1 1997
Externally publishedYes

Keywords

  • Androgen
  • Differential display
  • Mibolerone
  • Omithine decarboxylase
  • Prostate-specific antigen

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