Estrogen receptors (ER) in human breast cancer. The significance of a new prognostic factor based on both ER protein and ER mRNA contents

Cancer. 1994 Aug 1;74(3):864-71. doi: 10.1002/1097-0142(19940801)74:3<864::aid-cncr2820740312>3.0.co;2-n.

Abstract

Background: The response to endocrine therapy is not entirely predictable from the estrogen receptor (ER) and progesterone receptor (PgR) status of primary breast tumors. The authors previously proposed a new prognostic factor, ER.R, which was based on both ER protein and mRNA levels. A previous analysis of 88 primary breast carcinomas showed that ER.R permits the identification of a subset of ER-positive women with a higher risk of early relapse. The purpose of the present study was to confirm the prognostic significance of ER.R.

Methods: Estrogen receptor protein levels were determined for 171 patients with primary breast cancer either by radio-ligand binding assay (ER-LBA) or enzyme immunoassay (ER-EIA). Estrogen receptor, pS2, and c-erbB-2 mRNA were measured by Northern blot analysis.

Results: ER.R factor is determined by calculating the ratio of the values (ER protein in fentomoles per milligram of total proteins) to (ER mRNA in picograms per 4 micrograms of total RNA). A cutoff value of 1.5 (protein levels measured by ER-LBA) or 3 (protein levels measured by ER-EIA) discriminate the two ER.R1 (lower ratio) and ER.R2 (higher ratio) subgroups, which present a significantly lower and higher risk of early relapse, respectively. No association was found between ER.R status and either PgR status or c-erbB-2 and pS2 expression. According to a Cox multivariate analysis for disease free survival, the two stronger factors in predicting a poor prognosis were c-erbB-2 overexpression and ER.R2. In the present analysis, ER.R2 was a stronger predictor of recurrence than was ER negativity.

Conclusions: In accordance with the authors' first published data, the analysis of a larger population with a longer follow-up showed that ER.R2 keeps its significance to predict a poorer outcome for a patient, regardless of which assay was used to quantify ER.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Breast Neoplasms / chemistry*
  • Breast Neoplasms / mortality
  • Carrier Proteins / analysis*
  • ErbB Receptors / analysis
  • Female
  • Humans
  • Immunoenzyme Techniques
  • Prognosis
  • Proto-Oncogene Proteins / analysis
  • RNA, Messenger / analysis*
  • Radioligand Assay
  • Receptor, ErbB-2
  • Receptors, Estrogen / analysis*
  • Receptors, Estrogen / genetics*

Substances

  • Carrier Proteins
  • Proto-Oncogene Proteins
  • RNA, Messenger
  • Receptors, Estrogen
  • estrophilin
  • ErbB Receptors
  • Receptor, ErbB-2