Changes in tissue transglutaminase activity and expression during retinoic acid-induced growth arrest and apoptosis in primary cultures of human epithelial prostate cells

J Clin Endocrinol Metab. 1999 Apr;84(4):1463-9. doi: 10.1210/jcem.84.4.5593.


We treated primary epithelial cells from human normal prostate (NEPC) and prostate cancer (CEPC) with all-trans-retinoic acid (RA) to study whether it regulates the activity of tissue transglutaminase (tTGase), an enzyme that accumulates in cells undergoing apoptosis. tTGase activity was assessed by [14C]spermidine incorporation; tTGase, P53, Bcl-2, and p21 protein levels were evaluated by Western blotting; and RA receptors (RAR alpha, -beta, and -gamma), tTGase, retinol-binding protein (RBP), and cellular RBP type I transcripts were determined by semiquantitative RT-PCR. After 72-96 h of 10(-6) mol/L RA treatment, cell growth inhibition and apoptosis were associated with increased tTGase activity in both NEPC and CEPC, and with increased tTGase protein and messenger ribonucleic acid levels only in NEPC. Moreover, RA down-regulated RAR alpha and -beta and increased RBP messenger ribonucleic acid levels in NEPC, whereas it increased RAR beta gene expression and decreased Bcl-2 protein levels in CEPC. Our results suggest that RA induces tTGase gene expression and enzyme activity in normal prostate cells, and that RA-regulated pathways are impaired in cancer cells. Moreover, down-regulation of Bcl-2 protein and up-regulation of RAR beta suggest that retinoid may act on the genetic defect responsible for prostate cancer progression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / drug effects*
  • Cell Division / drug effects
  • Cells, Cultured
  • Epithelial Cells / drug effects
  • Epithelial Cells / enzymology
  • Epithelial Cells / pathology
  • Gene Expression Regulation, Enzymologic / drug effects
  • Humans
  • Male
  • Prostate / drug effects*
  • Prostate / enzymology
  • Prostate / pathology
  • Proto-Oncogene Proteins c-bcl-2 / analysis
  • Receptors, Retinoic Acid / physiology
  • Retinoic Acid Receptor alpha
  • Transglutaminases / genetics
  • Transglutaminases / metabolism*
  • Tretinoin / pharmacology*
  • Tumor Suppressor Protein p53 / analysis


  • Proto-Oncogene Proteins c-bcl-2
  • RARA protein, human
  • Receptors, Retinoic Acid
  • Retinoic Acid Receptor alpha
  • Tumor Suppressor Protein p53
  • retinoic acid receptor beta
  • Tretinoin
  • Transglutaminases