Interaction between estradiol and cAMP in the regulation of specific gene expression

Mol Cell Endocrinol. 1996 Nov 29;124(1-2):71-7. doi: 10.1016/s0303-7207(96)03930-5.

Abstract

The mRNA levels of LIV-1 and pS2, two estrogen-responsive genes, are increased by the agents, cholera toxin (CT) plus 3-isobutyl-l-methylxanthine (IBMX), which cause an increase in cAMP in MCF-7 human breast cancer cells. The simultaneous addition of estradiol and CT/IBMX results in a synergistic induction of the two mRNAs. The changes in mRNA reflect changes in transcription of the two genes. Interestingly, the addition of CT/IBMX to estradiol not only causes a greater increase in transcription rate but the increase is longer-lasting that seen with the hormone alone. Stimulation of mRNA levels by CT/IBMX, but not by estradiol, was prevented by cycloheximide. Stimulation by both estradiol and by CT/IBMX was prevented by the antiestrogen, ICI 164387. Transcription of LIV-1 and pS2 genes is by both estradiol and cAMP, via separate mechanisms both requiring the estrogen receptor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 1-Methyl-3-isobutylxanthine / pharmacology
  • Breast Neoplasms
  • Carcinoma
  • Cholera Toxin / pharmacology
  • Cyclic AMP / physiology*
  • Cycloheximide / pharmacology
  • Estradiol / analogs & derivatives
  • Estradiol / pharmacology*
  • Estrogen Antagonists / pharmacology
  • Gene Expression Regulation, Neoplastic / drug effects
  • Gene Expression Regulation, Neoplastic / physiology*
  • Humans
  • Neoplasm Proteins / genetics*
  • Phosphodiesterase Inhibitors / pharmacology
  • Polyunsaturated Alkamides
  • Protein Synthesis Inhibitors / pharmacology
  • Proteins*
  • RNA, Messenger / biosynthesis
  • RNA, Neoplasm / biosynthesis
  • Receptors, Estradiol / physiology
  • Trefoil Factor-1
  • Tumor Cells, Cultured
  • Tumor Suppressor Proteins

Substances

  • Estrogen Antagonists
  • Neoplasm Proteins
  • Phosphodiesterase Inhibitors
  • Polyunsaturated Alkamides
  • Protein Synthesis Inhibitors
  • Proteins
  • RNA, Messenger
  • RNA, Neoplasm
  • Receptors, Estradiol
  • TFF1 protein, human
  • Trefoil Factor-1
  • Tumor Suppressor Proteins
  • Estradiol
  • ICI 164384
  • Cholera Toxin
  • Cycloheximide
  • Cyclic AMP
  • 1-Methyl-3-isobutylxanthine