2-Methoxyestradiol--a unique blend of activities generating a new class of anti-tumour/anti-inflammatory agents

Research output: Contribution to journalArticle

  • External authors:
  • Robin L Anderson
  • Richard A Hughes
  • Emile Altmann
  • Michael Schuliga
  • James Ziogas
  • Alastair G Stewart


The estradiol metabolite, 2-methoxyestradiol (2MEO), is currently being evaluated in Phase II clinical trials for the treatment of solid tumours and is undergoing preclinical evaluation for inflammatory conditions. The anti-proliferative/cytotoxic/pro-apoptotic effects on tumour and endothelial cells have conferred potential on this metabolite for a synergistic impact on tumour growth. Exploitation of this synergy of 2MEO has previously required the combination of well-established cytotoxic agents with newer anti-angiogenic agents. This article reviews the pharmacology of 2MEO and describes the limitations inherent in its residual estrogen receptor affinity. The extent to which the metabolite 2MEO embodies an optimised therapeutic candidate is discussed. The challenges involved in using rational (3D QSAR-based) drug design to optimise the activity profile of analogues of 2MEO to provide additional members of this new class of anti-tumour/anti-inflammatory drug are also outlined.

Bibliographical metadata

Original languageEnglish
Pages (from-to)577-84
Number of pages8
JournalDrug discovery today
Issue number13-14
Publication statusPublished - Jul 2007