Low-dose environmental endocrine disruptors, increase aromatase activity, estradiol biosynthesis and cell proliferation in human breast cells.

Abstract

BACKGROUND:

Phenolic endocrine-disrupting compounds (EDCs) have long been suspected of increasing human breast cancer risk, via aromatase up-regulation; however, the metabolic effects upon aromatase in human breast cells exposed to environmentally relevant concentrations of phenolic compounds, have not been addressed.

OBJECTIVES:

To examine the mechanistic responses of aromatase CYP19A1 mRNA, aromatase activity, estradiol biosynthesis and cellular proliferation, in three human breast cell lines, exposed to seven phenolic compounds, at environmentally relevant concentrations.

METHODS:

MCF-7 and ZR-75-1 breast cancer cells, and HMF3A breast fibroblasts were treated with specific concentrations of p,p'-DDT, methoxychlor, benzophenone-2, bisphenol A, bisphenol S, 4-phenylphenol and n-butylparaben, with and without the presence of aromatase inhibitors and estrogen receptor inhibitors.

RESULTS:

All test EDCs up-regulated aromatase mRNA, increased aromatase activity, significantly increased the aromatase-induced biosynthesis of the breast carcinogen 17β-estradiol, and increased ERα-positive breast cell proliferation.

CONCLUSION:

Inadvertent exposures to 'phenolic' EDCs, increase estradiol biosynthesis, and estrogen-sensitive breast cancer proliferation.

• Authors: Graeme P Williams, Philippa D Darbre
• Journal: Molecular and cellular endocrinology (Mol Cell Endocrinol) Vol. 486 Pg. 55-64 (04 15 2019) ISSN: 1872-8057 [Electronic] Ireland
• PMID: 30817981 (Publication Type: Journal Article)
• Copyright: Copyright © 2019 Elsevier B.V. All rights reserved.

Chemical References

• Endocrine Disruptors
• RNA, Messenger
• Receptors, Estrogen
• Fulvestrant
• Testosterone
• Estradiol
• Letrozole
• Aromatase

Topics

• Aromatase (genetics, metabolism)
• Breast (pathology)
• Cell Line, Tumor
• Cell Proliferation (drug effects)
• Endocrine Disruptors (chemistry, toxicity)
• Estradiol (biosynthesis)
• Female
• Fulvestrant (pharmacology)
• Humans
• Letrozole (pharmacology)
• RNA, Messenger (genetics, metabolism)
• Receptors, Estrogen (metabolism)
• Testosterone (pharmacology)