Synthesis and Pharmacological Effects of the Anti-Cancer Agent 2-Methoxyestradiol

Curr Pharm Des. 2015;21(38):5453-66. doi: 10.2174/1381612821666151002112511.

Abstract

The endogenous steroid 2-methoxyestradiol (2-ME) is a metabolite of 17β-estradiol and its biosynthesis is well established. Moreover, 2-ME is also biosynthesized from estrone. For several years, 2-ME was perceived as an inactive metabolite devoid of any interesting biological activities. Since the late 1980s, a number of biological and pharmacological studies have revealed that 2-ME possesses interesting anti-cancer effects without any undesirable estrogen activity. In particular, the anti-vascular effects and anti-angiogenic activities that 2-ME exhibit, are of great interest and importance, in view of the development of new anti-cancer drugs based on 2-ME. Several clinical trial development programs have been initiated using the steroid 2-ME. In addition, based on the many pharmacological activities reported for 2-ME, but also due to the general interest in total and semi-synthesis of endogenous steroids, several research groups working with organic synthesis have prepared this steroid. Herein, the anti-cancer effects, the results from the clinical trial development programs and the synthetic studies towards 2-ME, are reviewed.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • 2-Methoxyestradiol
  • Animals
  • Antineoplastic Agents / chemical synthesis*
  • Antineoplastic Agents / pharmacology*
  • Antineoplastic Agents / therapeutic use
  • Cell Line, Tumor
  • Clinical Trials as Topic / methods
  • Estradiol / analogs & derivatives*
  • Estradiol / chemical synthesis
  • Estradiol / pharmacology
  • Estradiol / therapeutic use
  • Humans
  • Neoplasms / drug therapy
  • Receptors, Estrogen / antagonists & inhibitors
  • Treatment Outcome

Substances

  • Antineoplastic Agents
  • Receptors, Estrogen
  • Estradiol
  • 2-Methoxyestradiol