Carcinoma cell lines resistant for growth inhibition and apoptosis to retinoic acid are responsive to 4-hydroxy-phenyl-retinamide: correlation with tissue transglutaminase

Biochem Biophys Res Commun. 1999 Jan 27;254(3):636-41. doi: 10.1006/bbrc.1998.9987.

Abstract

Retinoic acid (RA)-resistant cell lines are highly malignant. To inhibit the growth of the RA-resistant cells we used 4-HPR, a synthetic retinoid, which may act through alternative signal transduction pathways. 4-HPR induced cell growth inhibition and apoptosis in all RA-sensitive as well as -resistant cells, demonstrating a wider spectrum of potency over RA. 4-HPR induced tissue TGase activity. A tight correlation between the induction of tissue TGase, the inhibition of cell growth, and apoptosis was evident in all eight RA-sensitive cell lines. However, basal TGase differed in the different cells, suggesting inducibility rather than basal levels as the relevant parameter. In sharp contrast to the RA-sensitive cells, RA-resistant cells showed sporadic response to 4-HPR for tissue TGase. The wider spectrum of activity of 4-HPR in inhibiting cell growth and inducing apoptosis makes it a good candidate for the treatment of RA-resistant cancer cells.

MeSH terms

  • 3T3 Cells
  • Animals
  • Apoptosis / drug effects
  • Carcinoma / enzymology
  • Carcinoma / pathology*
  • Cell Division / drug effects
  • Fenretinide / pharmacology*
  • Humans
  • Mice
  • Transglutaminases / metabolism*
  • Tretinoin / pharmacology*
  • Tumor Cells, Cultured

Substances

  • Fenretinide
  • Tretinoin
  • Transglutaminases