Quantitative analysis of estrogen receptor-beta mRNA and its variants in human breast cancers

Int J Cancer. 2000 Dec 1;88(5):733-6. doi: 10.1002/1097-0215(20001201)88:5<733::aid-ijc8>3.0.co;2-m.

Abstract

We have carried out a quantitative analysis of ER-alpha and ER-beta mRNA expression in normal (n = 11) and breast cancer (n = 112) tissues using a real-time (Taq-Man) PCR assay. Expression of ER-beta mRNA variants has also been studied by triple-primer PCR assay. ER-alpha mRNA levels in normal breast tissues were significantly (p < 0.01) lower than those in ER-positive breast cancers but not significantly different from those in ER-negative breast cancers. However, ER-beta mRNA levels in normal breast tissues were significantly (p < 0.01) higher than those in ER-positive and ER-negative breast cancers. Proportions of ER-beta1 and ER-beta2 mRNA expression among total ER-beta mRNA expression were significantly higher and those of ER-beta5 and ER-beta5; mRNA were significantly lower in normal breast tissues than in ER-positive and ER-negative breast cancers. ER-beta mRNA levels and proportions of ER-beta mRNA variants did not show any significant correlation with age, tumor size, lymph node status and histological grade. Our results demonstrate that ER-alpha mRNA is up-regulated and ER-beta mRNA is down-regulated during carcinogenesis of breast cancers. Changes in proportions of ER-beta mRNA variants are also implicated in this process.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Alternative Splicing*
  • Breast Neoplasms / diagnosis
  • Breast Neoplasms / genetics*
  • Estrogen Receptor alpha
  • Estrogen Receptor beta
  • Female
  • Genetic Markers
  • Genetic Variation
  • Humans
  • Middle Aged
  • Polymerase Chain Reaction
  • Prognosis
  • RNA, Messenger / analysis
  • Receptors, Estrogen / analysis*
  • Receptors, Estrogen / biosynthesis
  • Receptors, Estrogen / genetics

Substances

  • Estrogen Receptor alpha
  • Estrogen Receptor beta
  • Genetic Markers
  • RNA, Messenger
  • Receptors, Estrogen