Reduced levels of 5-α reductase 2 in adult prostate tissue and implications for BPH therapy

Prostate. 2011 Sep;71(12):1317-24. doi: 10.1002/pros.21348. Epub 2011 Feb 9.

Abstract

Background: 5-α reductase 2 (5-AR 2) is a key enzyme that is responsible of proper development of prostate tissue. Inhibition of 5-AR 2 has proven to be efficacious for management of urinary symptoms secondary benign prostatic hyperplasia (BPH). However, some patients are resistant to the therapeutic effects of 5-AR 2 inhibitor. We wished to determine why some benign non-cancerous adult human prostates do not express 5-AR 2, and hypothesized that methylation of 5-AR 2 promoter region correlated with low expression of 5-AR 2 protein.

Methods: The transition zone of 42 human prostate tissues after radical prostatectomy was used for evaluation. Initially, 21 paraffin embedded samples were used to assess immunoreactivity to 5-AR 2 antibody in non-cancerous BPH samples. In the next 21 samples, fresh frozen prostate transition zone samples without cancer were assessed for immunoreactivity and methylation of the 5-AR 2 promoter using methyl-specific PCR.

Results: We show that 6/21 (29%) of benign human prostate samples did not express the 5-AR 2 protein. Moreover, the promoter region of 5-AR 2 contains a CpG island that is methylated in benign prostate epithelial cells in culture and also in 39% (7/18) human prostate tissues. We show a strong correlation between methylation of the 5-AR 2 promoter region and absence of 5-AR 2 protein expression (P = 0.0025, Fisher's exact test).

Conclusions: Methylation of 5-AR 2 promoter may account for low or absent expression of 5-AR 2 in some human adult prostate tissues.

MeSH terms

  • Aged
  • Cell Line, Transformed
  • Cholestenone 5 alpha-Reductase / genetics
  • Cholestenone 5 alpha-Reductase / metabolism*
  • CpG Islands
  • DNA Methylation
  • Down-Regulation
  • Epithelial Cells / metabolism
  • Gene Expression
  • Humans
  • Immunohistochemistry
  • Isoenzymes / genetics
  • Isoenzymes / metabolism
  • Male
  • Middle Aged
  • Promoter Regions, Genetic
  • Prostate / enzymology*
  • Prostatic Hyperplasia / enzymology*
  • Prostatic Hyperplasia / genetics
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • Isoenzymes
  • Cholestenone 5 alpha-Reductase