[Estrogen receptor expression in tumors different from breast cancer]

Antibiot Khimioter. 2009;54(7-8):41-9.
[Article in Russian]

Abstract

A review of the literature data on expression of estrogen receptor alpha and beta (ERalpha and ERbeta) in tumors different from breast cancer. The results regarding the ERalpha and ERbeta expression frequency in non-small cell and small cell lung cancer, colorectal cancer, esophageal, ovarian, prostate and brain tumors are presented. High frequency of estrogen receptor expression (in up to 50 and more per cent of cases) in various types of tumors, differences between ERalpha and ERbeta in expression frequency, prognostic significance and prediction of the neoplastic process aggressiveness as well as in biological implications of interaction with antiestrogens (antagonistic and/or agonistic effect) are shown. The data on comparative evaluation of ERalpha and ERbeta expression in lung, ovarian, prostate tumor cells and corresponding nonneoplastic tissues are reported. Authors consider necessary to include the ERalpha and ERbeta detection into the routine clinical practice not only in breast cancer but in other tumors as well. Prospects of the clinical application of antiestrogens, in particular tamoxifen, in adjuvant therapy of different tumors with positive ER status are discussed.

Publication types

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

MeSH terms

  • Biomarkers, Tumor / analysis
  • Biomarkers, Tumor / metabolism*
  • Breast Neoplasms / diagnosis
  • Breast Neoplasms / drug therapy
  • Breast Neoplasms / metabolism
  • Chemotherapy, Adjuvant
  • Estrogen Receptor alpha / analysis
  • Estrogen Receptor alpha / metabolism*
  • Estrogen Receptor beta / analysis
  • Estrogen Receptor beta / metabolism*
  • Female
  • Humans
  • Male
  • Neoplasms / diagnosis*
  • Neoplasms / drug therapy
  • Neoplasms / metabolism*
  • Prognosis
  • Selective Estrogen Receptor Modulators / therapeutic use
  • Tamoxifen / therapeutic use

Substances

  • Biomarkers, Tumor
  • Estrogen Receptor alpha
  • Estrogen Receptor beta
  • Selective Estrogen Receptor Modulators
  • Tamoxifen