CELL Unit, de Duve Institute and Université Catholique de Louvain, B-1200 Brussels, Belgium.
GEPI Unit, de Duve Institute and Université Catholique de Louvain, B-1200 Brussels, Belgium.
Biomolecules. 2021 Oct 6;11(10):1472. doi: 10.3390/biom11101472.
An inappropriate response to progestogens in the human endometrium can result in fertility issues and jeopardize progestin-based treatments against pathologies such as endometriosis. PGRMC1 can mediate progesterone response in the breast and ovaries but its endometrial functions remain unknown. AG-205 is an alleged PGRMC1 inhibitor but its specificity was recently questioned. We added AG-205 in the cultures of two endometrial cell lines and performed a transcriptomic comparison. AG-205 significantly increased expression of genes coding enzymes of the cholesterol biosynthetic pathway or of steroidogenesis. However, these observations were not reproduced with cells transfected with siRNA against PGRMC1 or its related proteins (MAPRs). Furthermore, AG-205 retained its ability to increase expression of selected target genes even when expression of PGRMC1 or all MAPRs was concomitantly downregulated, indicating that neither PGRMC1 nor any MAPR is required to mediate AG-205 effect. In conclusion, although AG-205 has attractive effects encouraging its use to develop therapeutic strategies, for instance against breast cancer, our study delivers two important warning messages. First, AG-205 is not specific for PGRMC1 or other MAPRs and its mechanisms of action remain unclear. Second, due to its effects on genes involved in steroidogenesis, its use may increase the risk for endometrial pathologies resulting from imbalanced hormones concentrations.
人类子宫内膜对孕激素的反应不当可能导致生育问题,并危及孕激素为基础的治疗方法,如子宫内膜异位症。PGRMC1 可以介导孕激素在乳腺和卵巢中的反应,但它在子宫内膜中的功能仍然未知。AG-205 是一种据称的 PGRMC1 抑制剂,但最近其特异性受到质疑。我们在两种子宫内膜细胞系的培养物中添加了 AG-205,并进行了转录组比较。AG-205 显著增加了编码胆固醇生物合成途径或类固醇生成酶的基因的表达。然而,用针对 PGRMC1 或其相关蛋白 (MAPRs) 的 siRNA 转染的细胞并未重现这些观察结果。此外,即使同时下调 PGRMC1 或所有 MAPRs 的表达,AG-205 仍保留其增加选定靶基因表达的能力,表明介导 AG-205 作用既不需要 PGRMC1 也不需要任何 MAPR。总之,尽管 AG-205 具有令人鼓舞的作用,鼓励其用于开发治疗策略,例如治疗乳腺癌,但我们的研究提供了两个重要的警告信息。首先,AG-205 对 PGRMC1 或其他 MAPRs 并不特异,其作用机制仍不清楚。其次,由于其对参与类固醇生成的基因的影响,其使用可能会增加由于激素浓度失衡而导致的子宫内膜病变的风险。