The SEEM: Selective Estrogen Enzyme Modulators in breast cancer
- 1 January 1999
- journal article
- research article
- Published by Taylor & Francis in Gynecological Endocrinology
- Vol. 13 (sup6) , 1-8
- https://doi.org/10.1080/gye.13.s6.1.8
Abstract
Human breast cancer tissue contains all the enzymes (estrone sulfatase ,17 g -hydroxysteroid dehydrogenase ,aromatase) involved in the last steps of estradiol biosynthesis. This tissue also contains sulfotransferase for the formation of the biologically inactive estrogen sulfates. In the past years ,it has been demonstrated that various progestins (promegestone ,nomegestrol acetate ,medrogestone) as well as tibolone and its metabolites are potent inhibitors of sulfatase and 17 g -hydroxysteroid dehydrogenase activities. It was also shown that medrogestone ,nomegestrol acetate ,promegestone or tibolone can stimulate the sulfotransferase activity for the local production of estrogen sulfates. All these data ,in addition to numerous agents which can block the aromatase action ,lead to the new concept of Selective Estrogen Enzyme Modulators (SEEM) which can largely apply to breast cancer tissue. The exploration of various progestins and other active agents in trials with breast cancer patients ,showing an inhibitory effect on sulfatase and 17 g -hydroxysteroid dehydrogenase ,or a stimulatory effect on sulfotransferase ,will provide a new option in the treatment of this disease.Keywords
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