Endocrine Abstracts

Progesterone receptors (PR) are long recognized to suppress estrogen receptor (ER) mediated transcription in breast cancers. However, a mechanistic basis for this repression has been lacking. Recent reports indicate this occurs, in part, through global repositioning of ER on chromatin in the presence of selective PR modulators (SPRMS), both agonists and antagonists [1, 2]. The goal of our studies was to further understand the mechanisms by which PR impacts estrogen-dependent g...