ESR1 ligand-binding domain mutations in hormone-resistant breast cancer Academic Article uri icon

Overview

MeSH Major

  • Antineoplastic Agents, Hormonal
  • Breast Neoplasms
  • Drug Resistance, Neoplasm
  • Estrogen Receptor alpha
  • Mutation, Missense
  • Protein Interaction Domains and Motifs

abstract

  • Seventy percent of breast cancers express estrogen receptor (ER), and most of these are sensitive to ER inhibition. However, many such tumors for unknown reasons become refractory to inhibition of estrogen action in the metastatic setting. We conducted a comprehensive genetic analysis of two independent cohorts of metastatic ER-positive breast tumors and identified mutations in ESR1 affecting the ligand-binding domain (LBD) in 14 of 80 cases. These included highly recurrent mutations encoding p.Tyr537Ser, p.Tyr537Asn and p.Asp538Gly alterations. Molecular dynamics simulations suggest that the structures of the Tyr537Ser and Asp538Gly mutants involve hydrogen bonding of the mutant amino acids with Asp351, thus favoring the agonist conformation of the receptor. Consistent with this model, mutant receptors drive ER-dependent transcription and proliferation in the absence of hormone and reduce the efficacy of ER antagonists. These data implicate LBD-mutant forms of ER in mediating clinical resistance to hormonal therapy and suggest that more potent ER antagonists may be of substantial therapeutic benefit.

publication date

  • December 2013

Research

keywords

  • Academic Article

Identity

Language

  • eng

PubMed Central ID

  • PMC3903423

Digital Object Identifier (DOI)

  • 10.1038/ng.2822

PubMed ID

  • 24185512

Additional Document Info

start page

  • 1439

end page

  • 45

volume

  • 45

number

  • 12