Overview of PROTACs Targeting the Estrogen Receptor: Achievements for Biological and Drug Discovery

Curr Med Chem. 2022;29(22):3922-3944. doi: 10.2174/0929867328666211110101018.

Abstract

Estrogen receptors (ERs) are steroid hormone receptors, which belong to a large nuclear receptor family. Endocrine diseases correlate strongly with dysregulated ER signaling. Traditional therapies continue to rely on small molecule inhibitors, including aromatase inhibitors (AIs) and selective estrogen receptor modulators (SERMs), all of which permit acquired resistance to endocrine therapy. Proteolytic targeting chimeras (PROTACs) offer unprecedented potential for solving acquired endocrine resistance. ARV-471, an ER-targeting PROTAC developed by Arvinas, was designated as an Investigational New Drug by the US FDA in 2019, and a phase I trial in patients suffering from locally advanced or metastatic ER-positive/HER2- negative breast cancer was initiated. In this review, we will focus on progress in developing ER-targeting PROTACs from publications and patents aimed at the treatment of endocrine diseases.

Keywords: DNA binding region; ER-α; ER-β; Estrogen receptors (ERs); PROTACs; nuclear receptor (NR).

Publication types

  • Review

MeSH terms

  • Aromatase Inhibitors / therapeutic use
  • Breast Neoplasms* / drug therapy
  • Drug Discovery
  • Drug Resistance, Neoplasm
  • Female
  • Humans
  • Receptors, Estrogen*
  • Selective Estrogen Receptor Modulators* / therapeutic use

Substances

  • Aromatase Inhibitors
  • Receptors, Estrogen
  • Selective Estrogen Receptor Modulators