Arsenic and 17-β-estradiol bind to each other and neutralize each other’s signaling effects

dc.contributor.authorKumar, Sukhdeep
dc.contributor.authorGuptasarma, P.
dc.date.accessioned2020-12-02T07:16:58Z
dc.date.available2020-12-02T07:16:58Z
dc.date.issued2016
dc.descriptionOnly IISERM authors are available in the record.
dc.description.abstractWe report that arsenic trioxide (ATO) and 17-beta-estradiol (E2) abolish each other’s independent cell signaling effects in respect of cell survival and proliferation/migration of breast cancer (MCF-7) cells. The possibility that this is due to binding of ATO to E2 was confirmed through difference absorption spectroscopy, chromatography-coupled voltammometry and 1-D 1H and 13C NMR spectroscopy. Binding leads to attenuation of E2’s hydroxyl 1H peaks at its C17 and C3 carbon positions. The results suggest that ATO and E2 can titrate each other’s levels, potentially explaining why sustained arsenic exposure tends to be associated with delays in age of menarche, advanced age of menopause, poorer sperm quality, higher overall morbidity in men, and lower incidences of breast cancer in women in some arsenic-contaminated areas.en_US
dc.identifier.citationBiochemical and Biophysical Research Communications, 477(4),pp. 575-580.en_US
dc.identifier.otherhttps://doi.org/10.1016/j.bbrc.2016.06.087
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0006291X16310051
dc.identifier.urihttp://hdl.handle.net/123456789/2490
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectArsenicen_US
dc.subjectEstrogenen_US
dc.subjectEndocrinologyen_US
dc.subjectReproductionen_US
dc.titleArsenic and 17-β-estradiol bind to each other and neutralize each other’s signaling effectsen_US
dc.typeArticleen_US

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