Abstract
AbstractEndometriosis is a chronic inflammatory condition characterised by the presence of ectopic endometrial-like tissue (lesions), associated reduced fertility and chronic pain. Impacting both the health and psycho-social functioning of millions of women worldwide, there is an urgent need for innovative non-hormonal, non-invasive treatments for the disorder. Both peritoneal and lesion-resident macrophages have been strongly implicated in the pathogenesis of endometriosis; key roles include promotion of lesion growth, neuroangiogenesis and nerve sensitization. With such a central role in the disease, macrophages represent a novel therapeutic target. In the current preclinical study, we sought to repurpose the macrophage targeting anti-cancer drug RRx-001 for the treatment of endometriosis. We utilised mouse models of induced endometriosis to demonstrate that RRx-001 acts to reduce endometriosis lesions and attenuate associated pain-like behaviours, without negatively impacting fertility. Using single nuclei multiome analyses, we identified a modification of macrophage subpopulations in the peritoneal cavity, specifically a reduced acquisition of a pro-disease phenotype and an accumulation of a pro-resolving phenotype. These observations signify the potential of RRx-001 as a novel therapeutic for endometriosis management.
Publisher
Cold Spring Harbor Laboratory