Assessing oestrogenic effects of brominated flame retardants hexabromocyclododecane and tetrabromobisphenol A on MCF-7 cells
Language English Country Czech Republic Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
21457653
PII: file/5737/fb2011a0007.pdf
Knihovny.cz E-resources
- MeSH
- Estrogen Receptor alpha metabolism MeSH
- Estrogen Antagonists toxicity MeSH
- Hydrocarbons, Brominated toxicity MeSH
- Endocrine Disruptors toxicity MeSH
- Estradiol analogs & derivatives metabolism MeSH
- Estrogens analysis MeSH
- Gene Expression MeSH
- Trefoil Factor-1 MeSH
- Fulvestrant MeSH
- Humans MeSH
- Cell Line, Tumor MeSH
- Tumor Suppressor Proteins metabolism MeSH
- Polybrominated Biphenyls toxicity MeSH
- Reverse Transcriptase Polymerase Chain Reaction MeSH
- Cell Proliferation MeSH
- Flame Retardants toxicity MeSH
- Up-Regulation MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Estrogen Receptor alpha MeSH
- Estrogen Antagonists MeSH
- Hydrocarbons, Brominated MeSH
- Endocrine Disruptors MeSH
- Estradiol MeSH
- Estrogens MeSH
- Trefoil Factor-1 MeSH
- Fulvestrant MeSH
- hexabromocyclododecane MeSH Browser
- Tumor Suppressor Proteins MeSH
- Polybrominated Biphenyls MeSH
- Flame Retardants MeSH
- tetrabromobisphenol A MeSH Browser
- TFF1 protein, human MeSH Browser
Tetrabromobisphenol A (TBBPA) is the main flame retardant used in printed circuit boards and laminates. The human population is highly exposed to TBBPA as it is used in consumer electronics as well as office and communication equipment. The main use of hexabromocyclododecane (HBCD) is in insulation foam boards, which are widely used in the construction sector. Brominated flame retardants may possess endocrine disrupting activity and thus represent a threat to the environment, including humans and their reproduction. The aim of this work was to evaluate the oestrogenic effects of TBBPA and HBCD in vitro on MCF-7 cells. We used the proliferation test (E-screen assay) in MCF-7 breast cancer cells and reverse transcription quantitative polymerase chain reaction analysis of TFF1 gene expression to analyse oestrogenicity of the studied compounds. RT-qPCR has proved to be a fast and valuable molecular technique in gene expression quantification. HBCD but not TBBPA increased cell proliferation in MCF-7 cells and up-regulated TFF1 gene expression in a concentration-dependent manner. Anti-oestrogen ICI 182,780 inhibited up-regulation of TFF1 by HBCD. We have shown that HBCD displays oestrogen- like effects on MCF-7 cells. TBBPA, on the other hand, has not shown any oestrogenic effect mediated by the oestrogen receptor α.