Ulipristalacetate treatment of endometriosis and normal endometrial stromal cells inhibits cell proliferation

In: Geburtshilfe und Frauenheilkunde · 2014 · vol. 74(S 01) · doi:10.1055/s-0034-1388550 · W2314477143
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AI-generated summary by claude@2026-06, 2026-06-09

Ulipristalacetate treatment was investigated and found to inhibit the proliferation of both normal endometrial stromal cells and endometriosis stromal cells in culture.

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The study examined whether ulipristal acetate (UPA), previously shown to block estradiol/progesterone-driven proliferation in normal endometrial cells, would also inhibit proliferation of endometriosis stromal cells. Researchers isolated stromal cells from a deep infiltrating endometriosis lesion and from matched normal endometrium, confirmed steroid hormone receptor gene expression by semi-quantitative real-time PCR, and then measured proliferation after adding UPA (10–100 mM) followed by cell counts at 48 and 72 hours. UPA treatment at 50 µM produced the largest reduction in proliferation at 48 hours, decreasing proliferation more than 2-fold in both normal endometrial cells and endometriosis cells, despite endometriosis stromal cells showing much lower progesterone receptor (PGR) expression than matched normal endometrium. The paper relates to endometriosis by experimentally testing UPA’s antiproliferative effects on stromal cells derived from deep infiltrating endometriosis.

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Abstract

Question: Ulipristalacetate (UPA) has been previously demonstrated to inhibit the estradiol and progesterone induced proliferative response of normal endometrial cells in culture. We predicted that UPA would inhibit proliferation of endometriosis cells.
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Results

Both stromal cell lines were > 90% vimentin and 15% cytokeratin-7 positive using immunoflourescence microscopy and expressed steroid hormone receptors. Endometriosis stromal cells were only 30% estrogen receptor (ERa) and 10% PGR positive by gene expression compared to matched endometrial cells. Compared to untreated cells, 50mM UPA treatment at 48hr showed the highest decrease of cell proliferation for both normal endometrial (2.5-fold) and endometriosis cells (2.3-fold).

Conclusions

PGR as the target gene of UPA is highly expressed in normal and lowly expressed in endometriosis stromal cells. UPA at 50µM inhibits cell proliferation > 2-fold for both normal and endometriosis cells in culture. However, considering the major difference in PGR expression of control endometrium and endometriosis cells a similar cell proliferation inhibition was found.

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endometriosis

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