Retinoic acid and 1,25-dihydroxyvitamin D3 inhibit tenascin-C expression in rat glioma C6 cells

J Neurosci Res. 1999 Oct 15;58(2):293-300. doi: 10.1002/(sici)1097-4547(19991015)58:2<293::aid-jnr9>3.0.co;2-h.

Abstract

Tenascin-C (Tn-C) is an extracellular matrix protein with growth-, invasive-, and angiogenesis-promoting activities. Tn-C is upregulated during wound healing, tumorigenesis, and other pathological conditions. Highly malignant gliomas with poor prognosis exhibit high levels of Tn-C expression. Here we demonstrate that Tn-C RNA expression in glioma C6 cells is inhibited in a dose-dependent manner by retinoic acid (RA) and 1,25-dihydroxyvitamin D3 (1,25-D3). No additive or synergistic effects were found. Inhibition is maximum 24 hr after RA or 1,25-D3 treatment, prior to a delayed cytotoxic effect starting at day 4-5 of treatment, and correlates with a reduction in the synthesis of Tn-C protein. Tn-C expression is also inhibited, but to a lesser extent by prostaglandin D2 (PGD2). Furthermore, both RA and 1,25-D3, but not PGD2 abolish the induction of Tn-C by the tumor promoter 12-O-tetradecanoyl phorbol 13-acetate. The inhibition of Tn-C expression might be relevant for the anti-cancer activity of RA and 1,25-D3.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcitriol / pharmacology*
  • Carcinogens / toxicity
  • Drug Synergism
  • Glioma / drug therapy*
  • Glioma / metabolism
  • Glioma / pathology
  • Prostaglandin D2 / pharmacology
  • Rats
  • Receptors, Calcitriol / genetics
  • Tenascin / biosynthesis*
  • Tetradecanoylphorbol Acetate / toxicity
  • Tretinoin / pharmacology*
  • Up-Regulation

Substances

  • Carcinogens
  • Receptors, Calcitriol
  • Tenascin
  • Tretinoin
  • Calcitriol
  • Tetradecanoylphorbol Acetate
  • Prostaglandin D2