Article ID Journal Published Year Pages File Type
2599614 Toxicology Letters 2012 4 Pages PDF
Abstract

The fusarielins are a group of metabolites found in several Aspergillus and Fusarium species that have been reported to have with weak antifungal, antibiotic and cytotoxic effects. This study identifies fusarielin A, F, G and H isolated from Fusarium as mycoestrogens. Mycoestrogens are compounds from fungi that bind to the estrogen receptors and induce an estrogenic response in targeted cells. All four tested fusarielins stimulate MCF-7 cell proliferation with fusarielin H as the most potent, able to stimulate cell proliferation 4-fold in a resazurin metabolism assay at 25 μM. MDA-MB-231 cells without the estrogen receptor-α and MCF-10a cells without estrogen receptors were not stimulated by fusarielins. Furthermore, the stimulation was prevented in MCF-7 cells when fusarielins were incubated in the presence of the estrogen receptor antagonist fulvestrant. These observations suggest that fusarielins bind to the estrogen receptor and act as weak mycoestrogens.

► Fusarielins A, F, G and H stimulate MCF-7 cells. ► Fusarielins have no stimulating effect in MDA-MB-231 and MCF-10a cells. ► Fusarielins should be classified as mycoestrogens.

Related Topics
Life Sciences Environmental Science Health, Toxicology and Mutagenesis
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