Synergism between androgens and protein kinase-C on androgen-regulated gene expression

Mol Cell Endocrinol. 1995 Apr 28;110(1-2):R1-6. doi: 10.1016/0303-7207(95)03534-e.

Abstract

Androgen (R1881) induced transcriptional activity of the human androgen receptor, stably expressed in CHO cells, can be stimulated an extra 2-fold by the addition of the protein kinase C activator, 4 beta-phorbol 12-myristate 13-acetate (PMA). This extra stimulation is not observed when the protein kinase A activator bromoadenosine 3':5'-cyclic monophosphate (8-BrcAMP) is used. The transcriptional activity was measured using a reporter plasmid containing the MMTV-promoter, coupled to the luciferase gene. The effect of PMA on R1881-induced transcription was not due to a higher expression level of the androgen receptor. Also, no extra phosphorylation of the androgen receptor could be measured after incubation with PMA. When GRE-tk-LUC and PSA-LUC reporters were used, the synergistic effect of PMA could not be observed. The findings on the composite MMTV-LTR promoter can be explained by either a direct synergistic interaction between occupied AP-1 like responsive elements and the androgen receptor or via an unknown transcription factor activated by the PKC pathway and interacting with the androgen receptor.

MeSH terms

  • Animals
  • CHO Cells
  • Cricetinae
  • Drug Synergism
  • Enzyme Activation / drug effects
  • Gene Expression Regulation / drug effects*
  • Humans
  • Luciferases / genetics
  • Mammary Tumor Virus, Mouse / genetics
  • Metribolone / pharmacology*
  • Phosphorylation
  • Promoter Regions, Genetic
  • Protein Kinase C / metabolism*
  • Regulatory Sequences, Nucleic Acid
  • Tetradecanoylphorbol Acetate / pharmacology
  • Transcription, Genetic

Substances

  • Metribolone
  • Luciferases
  • Protein Kinase C
  • Tetradecanoylphorbol Acetate