Activity of MDI-301, a novel synthetic retinoid, in xenografts

Anticancer Drugs. 2004 Nov;15(10):991-6. doi: 10.1097/00001813-200411000-00009.

Abstract

The efficacy of MDI-301, a non-toxic novel synthetic retinoid, was found to be equivalent to the natural 9-cis-retinoic acid (RA) in vitro against estrogen-dependent MCF7 and T47D breast cancer cell lines which express RA receptor (RAR) alpha. Both retinoids also showed similar efficacy against established PC-3 prostate carcinoma xenografts. MCF7 tumor xenografts showed a reduction in tumor growth of 48% without systemic side-effects upon treatment with MDI-301 compared with MCF7 controls. Tumor xenografts derived from MDA-MB-231, an estrogen-independent breast cancer cell line that expresses low levels of RARalpha, were unresponsive. This study demonstrates that MDI-301 is as efficacious as 9-cis-RA against cancer cells with RARalpha, with no signs of toxicity in vivo, making it a potential candidate for cancer therapy.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Alitretinoin
  • Animals
  • Antineoplastic Agents / pharmacology*
  • Breast Neoplasms
  • Cell Line, Tumor
  • Female
  • Humans
  • Immunohistochemistry
  • Male
  • Mice
  • Mice, Nude
  • Prostatic Neoplasms
  • Receptors, Retinoic Acid / biosynthesis
  • Retinoic Acid Receptor alpha
  • Retinoids / pharmacology*
  • Tretinoin / pharmacology
  • Xenograft Model Antitumor Assays

Substances

  • Antineoplastic Agents
  • MDI 301
  • RARA protein, human
  • Rara protein, mouse
  • Receptors, Retinoic Acid
  • Retinoic Acid Receptor alpha
  • Retinoids
  • Alitretinoin
  • Tretinoin