The truncated estrogen receptor alpha variant lacking exon 5 is not involved in progesterone receptor expression in meningiomas

J Steroid Biochem Mol Biol. 1999 Dec 31;71(5-6):167-72. doi: 10.1016/s0960-0760(99)00141-7.

Abstract

Human meningioma tissues are mostly estrogen receptor (ER) negative and progesterone receptor (PR) positive in ligand binding and enzyme immuno assays. To explain this apparently ER independent PR expression, we investigated the existence of a 'hidden' ER variant, which would be capable of activating transcription of the PR gene. Total RNA of seven meningiomas, two breast cancer tissues and of MCF7 cells was analyzed by RT-PCR using primers situated in exon 4 and exon 6. Differential hybridization of the PCR transcripts with probes in exon 4 and 5 respectively, revealed a wild type ER (wtER) fragment and an exon 5 deleted ER variant (ERDelta5). PCR products of two meningiomas were cloned for sequence analysis. The result confirmed the existence of a wtER and ERDelta5.RT-PCR followed by Southern analysis was performed on mRNA of 23 meningiomas to determine the amount of ERDelta5 relative to wtER, which was compared to the PR content of the tissues. In contrast to our initial hypothesis and literature data on breast cancer, there was no relationship between the ERDelta5/wtER ratio and PR protein concentration. It is therefore concluded that ERDelta5 mRNA does not play the dominant role in PR synthesis in meningioma tissue.

MeSH terms

  • Blotting, Southern
  • Breast Neoplasms / genetics
  • Cloning, Molecular
  • Estrogen Receptor alpha
  • Exons
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Meningeal Neoplasms / genetics*
  • Meningeal Neoplasms / metabolism
  • Meningioma / genetics*
  • Meningioma / metabolism
  • RNA, Messenger / metabolism
  • Receptors, Estrogen / genetics*
  • Receptors, Progesterone / genetics*
  • Receptors, Progesterone / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sequence Analysis, DNA
  • Sequence Deletion*
  • Transcriptional Activation
  • Tumor Cells, Cultured

Substances

  • Estrogen Receptor alpha
  • RNA, Messenger
  • Receptors, Estrogen
  • Receptors, Progesterone