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Characterisation of the androgen regulation of glycine N-methyltransferase in prostate cancer cells.

Abstract
The development and growth of prostate cancer is dependent on androgens; thus, the identification of androgen-regulated genes in prostate cancer cells is vital for defining the mechanisms of prostate cancer development and progression and developing new markers and targets for prostate cancer treatment. Glycine N-methyltransferase (GNMT) is a S-adenosylmethionine-dependent methyltransferase that has been recently identified as a novel androgen-regulated gene in prostate cancer cells. Although the importance of this protein in prostate cancer progression has been extensively addressed, little is known about the mechanism of its androgen regulation. Here, we show that GNMT expression is stimulated by androgen in androgen receptor (AR) expressing cells and that the stimulation occurs at the mRNA and protein levels. We have identified an androgen response element within the first exon of the GNMT gene and demonstrated that AR binds to this element in vitro and in vivo. Together, these studies identify GNMT as a direct transcriptional target of the AR. As this is an evolutionarily conserved regulatory element, this highlights androgen regulation as an important feature of GNMT regulation.
AuthorsSilvia Ottaviani, Greg N Brooke, Ciara O'Hanlon-Brown, Jonathan Waxman, Simak Ali, Laki Buluwela
JournalJournal of molecular endocrinology (J Mol Endocrinol) Vol. 51 Issue 3 Pg. 301-12 (Dec 2013) ISSN: 1479-6813 [Electronic] England
PMID23997240 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Androgens
  • Receptors, Androgen
  • Glycine N-Methyltransferase
Topics
  • Androgens (metabolism)
  • Blotting, Western
  • Cell Line, Tumor
  • Chromatin Immunoprecipitation
  • Electrophoretic Mobility Shift Assay
  • Glycine N-Methyltransferase (metabolism)
  • Humans
  • Male
  • Microscopy, Confocal
  • Prostatic Neoplasms (enzymology, metabolism)
  • Real-Time Polymerase Chain Reaction
  • Receptors, Androgen (metabolism)

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