HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Optimization of an estrogen receptor-alpha transcriptional activation assay for testing a diverse spectrum of chemicals.

Abstract
Estrogen receptor (ER) transactivation assays were initially designed to study endogenous mechanisms of steroid hormone action, but more recently have been used to assess industrial chemicals for potential estrogenic activity. Given the diverse spectrum of physicochemical properties of these chemicals, we examined the effects of pH (a weak organic and strong inorganic acid and base), hyperosmolality (NaCl, mannitol) and two different vehicles (DMSO, Triton X-100) on responses to estradiol-17beta (E2) in an ER transactivation assay. MCF-7 human breast cancer cells were transiently transfected with a chimeric estrogen receptor (Gal4-HEG0) and a Gal4-regulated luciferase reporter gene (17m5-G-Luc), treated with E2 under various test conditions, and then assessed for ER-mediated luciferase activity. Maximal E2-induced reporter activity was observed at pH 7.8 (pre-incubation), but was markedly reduced at pH < or =7.5, or > or =8.0 (P < 0.001), even though there was no evidence of cytotoxicity. Hyperosmolality induced by addition of mannitol (> or =25 mM) resulted in significant decreases in overall assay responsiveness, whereas NaCl (> or =80 mM) decreased the sensitivity of the assay by increasing the no-observed-effect level for E2 compared to control cultures (330 mOsm). The maximal DMSO concentration that resulted in consistently high E(2)-induced reporter activity was 0.1%, whereas concentrations of Triton X-100 above 1 ppm inhibited E2-induced reporter responses and were cytotoxic above 10 ppm. These results indicate that various physicochemical factors have the potential to confound assay data if not kept within predefined operational limits.
AuthorsG D Charles, C Gennings, J Clemons, T R Zacharewski, B B Gollapudi, E W Carney
JournalJournal of applied toxicology : JAT (J Appl Toxicol) 2000 Nov-Dec Vol. 20 Issue 6 Pg. 449-54 ISSN: 0260-437X [Print] England
PMID11180266 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright 2000 John Wiley & Sons, Ltd.
Chemical References
  • Estradiol Congeners
  • Estrogen Receptor alpha
  • Receptors, Estrogen
  • Solvents
  • Estradiol
Topics
  • Cells, Cultured
  • Chemical Phenomena
  • Chemistry, Physical
  • Estradiol (toxicity)
  • Estradiol Congeners (toxicity)
  • Estrogen Receptor alpha
  • Female
  • Genes, Reporter
  • Humans
  • Hydrogen-Ion Concentration
  • Osmolar Concentration
  • Receptors, Estrogen (biosynthesis)
  • Solvents
  • Transcriptional Activation (drug effects)
  • Transfection

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: