Antiproliferative effects of progesterone antagonists and progesterone receptor modulators on the endometrium

• Published in: Steroids Vol. 65; no. 10; pp. 741 - 751
• Main Authors: Chwalisz, Kristof, Brenner, Robert M, Fuhrmann, Ulrike U, Hess-Stumpp, Holger, Elger, Walter
• Format: Journal Article Conference Proceeding
• Language: English
• Published: New York, NY Elsevier Inc 01.10.2000; Elsevier Science
• Subjects: Animals; Biological and medical sciences; Blood Vessels - drug effects; Cell Division - drug effects; Endometriosis; Endometrium; Endometrium - blood supply; Endometrium - cytology; Endometrium - drug effects; Female; Genital system. Reproduction; Hormone Antagonists - pharmacology; Humans; Medical sciences; Mesoprogestins; Pharmacology. Drug treatments; Progesterone; Progesterone - antagonists & inhibitors; Progesterone antagonist; Progesterone receptor modulators; Receptors, Estrogen - drug effects; Receptors, Estrogen - metabolism; Receptors, Progesterone - drug effects; Receptors, Progesterone - metabolism; Endometriosis; Progesterone; Progesterone antagonist; Progesterone receptor modulators; Endometrium; Mesoprogestins; Cell proliferation; Modulator; Antihormone; Review; Ovarian hormone; Progestagen; Uterus; Animal; Female genital system; Antiprogesterone; Antagonist; Sex steroid hormone; Hormonal receptor
• ISSN: 0039-128X; 1878-5867
• DOI: 10.1016/S0039-128X(00)00190-2

Progesterone antagonists (PAs, antiprogestins) can modulate estrogenic effects in various estrogen-dependent tissues. These modulatory effects are complex and depend on species, tissue, type of compound, dose, and duration of treatment. In non-human primates, PAs, including mifepristone, ZK 137 316 and ZK 230 211, inhibit endometrial proliferation and induce amenorrhea. When administered chronically at relatively low doses, these compounds block the mitotic activity of endometrial epithelium and induce stromal compaction in a dose-dependent manner in both spayed and intact monkeys at high estradiol concentrations. These effects were accompanied by an atrophy of spiral arteries. The antiproliferative effects were endometrium-specific, since the estrogenic effects in the oviduct and vagina were not inhibited by PAs. Similar endometrial antiproliferative effects were also found after treatment with the progesterone receptor modulator (PRM), mesoprogestin J1042. The endometrial antiproliferative effects of PAs, particularly within the endometrial glands, were also observed in spayed rabbits. In spayed rats, however, the PAs did not inhibit, but rather enhanced, various estrogen responses, including endometrial proliferation, pointing to species-specific differences. In conclusion, our studies indicate that both pure PAs and PRMs selectively inhibit estrogen-dependent endometrial proliferation in the primate endometrium without affecting estrogenic response in other estrogen-dependent tissues or inducing unscheduled bleeding. Our studies indicate that the spiral arteries, which are unique to the primate endometrium, are the primary targets that are damaged or inhibited by PAs and PRMs. The damage to these unique vessels may underlay the paradoxical, endometrium-specific, antiproliferative effects of these compounds. Hence, the properties of PAs and PRMs (mesoprogestins) open up new applications in gynecological therapy and hormone replacement therapy.