Estrogenic activity of zearalenone, α-zearalenol and β-zearalenol assessed using the E-screen assay in MCF-7 cells
- Toxicol Mech Methods. 2018 May;28(4):239-242. doi: 10.1080/15376516.2017.1395501.
- 1. a Laboratory of Toxicology, Department of Preventive Medicine, Faculty of Pharmacy , University of Valencia , Burjassot , Valencia , Spain.
- 2. b Laboratory of Toxicology, Department of Health Sciences , Biomedical Research Institute of Murcia (IMIB-UMU-Arrixaca), University Clinical Hospital "Virgen de la Arrixaca", University of Murcia , Murcia , Spain.
- 3. c Department of Biology , University of Turku , Turku , Finland.
Mycotoxins, including zearalenone (ZEA), can occur worldwide in cereals. They can enter the food chain and cause several health disorders. ZEA and its derivatives (α-zearalenol, α-ZOL and β-zearalenol, β-ZOL) have structural analogy to estrogen, thus they can bind to estrogen receptors (ERs). In order to characterize the estrogenic activity of ZEA, α-ZOL and β-ZOL, the proliferation of ER-positive human breast Cancer cells (MCF-7) exposed to these mycotoxins was measured. After exposure at levels ranging from 6.25 to 25 µM, cell proliferation was evaluated by using the E-Screen bioassay. In accordance with previous studies, our results show the estrogenic activity of ZEA, α-ZOL and β-ZOL in MCF-7 cells. This effect is related to ZEA and its metabolites being flexible enough to bind to mammalian ERs. The relative proliferative effect (RPE) ranged from 10% to 91%. The α-ZOL induced the highest proliferative effect due to its higher affinity for the ERs compared to the Other mycotoxins.
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Cat. No.Product NameDescriptionTargetResearch Area
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target: Estrogen Receptor/ERRResearch Areas: Inflammation/Immunology
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Research Areas: Inflammation/Immunology