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Many endocrine-disrupting chemicals (EDCs) interact with these SULTs as substrates and inhibitors, and thereby alter sulfation reactions responsible for metabolism and regulation of endocrine hormones such as estrogens and thyroid hormones. EDCs or their metabolites may also regulate expression of SULTs through direct interaction with nuclear receptors and other transcription factors. Moreover, some sulfate esters derived from EDCs (EDC-sulfates) may serve as ligands for endocrine hormone receptors. While the sulfation of an EDC can lead to its excretion in the urine or bile, it may also result in retention of the EDC-sulfate through its reversible binding to serum proteins and thereby enable transport to other tissues for intracellular hydrolysis and subsequent endocrine disruption. This mini-review outlines the potential roles of SULTs and sulfation in the effects of EDCs and our evolving understanding of these processes.<\/jats:p>","DOI":"10.1042\/ebc20230101","type":"journal-article","created":{"date-parts":[[2024,5,3]],"date-time":"2024-05-03T08:56:33Z","timestamp":1714726593000},"page":"541-553","update-policy":"https:\/\/doi.org\/10.1042\/crossmark_policy","source":"Crossref","is-referenced-by-count":11,"title":["Cytosolic sulfotransferases in endocrine disruption"],"prefix":"10.1042","volume":"68","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-6079-7459","authenticated-orcid":false,"given":"Michael\u00a0W.","family":"Duffel","sequence":"additional","affiliation":[{"name":"Department of Pharmaceutical Sciences & Experimental Therapeutics, College of Pharmacy, The University of Iowa, Iowa City, IA 52242, U.S.A."}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"288","published-online":{"date-parts":[[2024,12,4]]},"reference":[{"key":"2024120413510502100_B1","doi-asserted-by":"publisher","first-page":"401","DOI":"10.3109\/03602532.2013.835613","article-title":"Interactions of cytosolic sulfotransferases with xenobiotics","volume":"45","author":"James","year":"2013","journal-title":"Drug Metab. 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