HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Expression of estrogen receptor (ER) (beta)cx protein in ER(alpha)-positive breast cancer: specific correlation with progesterone receptor.

Abstract
Estrogen receptor (ER) (beta)cx, a splice variant of ERbeta, is a dominant repressor of ER(alpha) function. In this study we investigated the possibility that because the progesterone receptor (PR) gene is a downstream target of activated ER(alpha), in ER(alpha)-positive breast cancers, expression of ER(beta)cx would result in repression of PR. In ER(alpha)-positive MCF-7 cells, stable transfection of an ER(beta)cx expression vector resulted in reduced expression of PR without affecting ER(alpha) expression. In breast cancers, immunohistochemical evaluation of ER(alpha)-positive foci for the expression of PR and ER(beta)cx revealed a significant correlation between a PR-negative phenotype and the presence of ER(beta)cx within the foci. However, when entire lesions were evaluated by Allred scoring in 115 ER(alpha)-positive breast cancer specimens, the presence of two distinct groups of patients could be discerned. One group expressed ER(beta)cx and had very reduced levels of PR expression, as expected. The second group showed both ER(beta)cx and high levels of PR. To evaluate the role of ER(beta)cx in sensitivity to tamoxifen, 18 core needle biopsies, obtained before preoperative treatment with tamoxifen, were investigated. The results show that expression of ER(beta)cx in primary lesions correlated with a poor response to tamoxifen, especially in cancers with a low PR expression in Allred score. This is the first evidence that evaluation of ER(beta)cx along with PR may contribute to a better characterization of ER(alpha)-positive breast cancers.
AuthorsShigehira Saji, Yoko Omoto, Chikako Shimizu, Margaret Warner, Yukiko Hayashi, Shin-ichiro Horiguchi, Toru Watanabe, Shin-ichi Hayashi, Jan-Ake Gustafsson, Masakazu Toi
JournalCancer research (Cancer Res) Vol. 62 Issue 17 Pg. 4849-53 (Sep 01 2002) ISSN: 0008-5472 [Print] United States
PMID12208729 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antineoplastic Agents, Hormonal
  • Estrogen Receptor alpha
  • Estrogen Receptor beta
  • Protein Isoforms
  • Receptors, Estrogen
  • Receptors, Progesterone
  • Tamoxifen
Topics
  • Amino Acid Sequence
  • Antibody Specificity
  • Antineoplastic Agents, Hormonal (therapeutic use)
  • Breast Neoplasms (drug therapy, genetics, metabolism)
  • Estrogen Receptor alpha
  • Estrogen Receptor beta
  • Exons
  • Female
  • Humans
  • Immunohistochemistry
  • Middle Aged
  • Molecular Sequence Data
  • Predictive Value of Tests
  • Protein Isoforms (biosynthesis, genetics, immunology)
  • Receptors, Estrogen (biosynthesis, genetics, immunology)
  • Receptors, Progesterone (biosynthesis)
  • Tamoxifen (therapeutic use)
  • Transfection
  • Tumor Cells, Cultured

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: