{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,20]],"date-time":"2026-07-20T14:20:13Z","timestamp":1784557213542,"version":"3.55.0"},"reference-count":157,"publisher":"Bioscientifica","issue":"2","content-domain":{"domain":["jme.bioscientifica.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2018,8]]},"abstract":"<jats:p>\n                    Endometriosis is an incurable hormone-dependent inflammatory disease that causes chronic pelvic pain and infertility characterized by implantation and growth of endometrial tissue outside the uterine cavity. Symptoms have a major impact on the quality of life of patients resulting in socioeconomic, physical and psychological burdens. Although the immune system and environmental factors may play a role in the aetiology of endometriosis, oestrogen dependency is still considered a hallmark of the disorder. The impact of oestrogens such as oestrone and particularly, oestradiol, on the endometrium or endometriotic lesions may be mediated by steroids originating from ovarian steroidogenesis or local intra-tissue production (intracrinology) dependent upon the expression and activity of enzymes that regulate oestrogen biosynthesis and metabolism. Two key pathways have been implicated: while there is contradictory data on the participation of the aromatase enzyme (encoded by\n                    <jats:italic>CYP19A1<\/jats:italic>\n                    ), there is increasing evidence that the steroid sulphatase pathway plays a role in both the aetiology and pathology of endometriosis. In this review, we consider the evidence related to the pathways leading to oestrogen accumulation in endometriotic lesions and how this might inform the development of new therapeutic strategies to treat endometriosis without causing the undesirable side effects of current regimes that suppress ovarian hormone production.\n                  <\/jats:p>","DOI":"10.1530\/jme-17-0297","type":"journal-article","created":{"date-parts":[[2018,7,20]],"date-time":"2018-07-20T05:20:47Z","timestamp":1532064047000},"page":"T253-T270","update-policy":"https:\/\/doi.org\/10.1530\/crossmarkpolicy-6","source":"Crossref","is-referenced-by-count":11,"title":["SULFATION PATHWAYS: Contribution of intracrine oestrogens to the aetiology of endometriosis"],"prefix":"10.1530","volume":"61","author":[{"given":"Carla A","family":"Piccinato","sequence":"first","affiliation":[{"name":"1Hospital Israelita Albert Einstein, S\u00e3o Paulo, S\u00e3o Paulo, Brazil"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Helena","family":"Malvezzi","sequence":"additional","affiliation":[{"name":"1Hospital Israelita Albert Einstein, S\u00e3o Paulo, S\u00e3o Paulo, Brazil"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Douglas A","family":"Gibson","sequence":"additional","affiliation":[{"name":"2MRC Centre for Inflammation Research, The University of Edinburgh, Edinburgh, UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Philippa T K","family":"Saunders","sequence":"additional","affiliation":[{"name":"2MRC Centre for Inflammation Research, The University of Edinburgh, Edinburgh, UK"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"416","reference":[{"key":"ref891","doi-asserted-by":"crossref","first-page":"116","DOI":"10.1067\/mjd.2001.117432","article-title":"Estrogen production and action","volume":"45","year":"2001","journal-title":"Journal of the American Academy of 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