Effects of pharmacological inhibition of hyaluronic acid synthesis on experimental endometriosis. (16th November 2022)

• Record Type: Journal Article
• Authors: Olivares, Carla Noemí; Ricci, Analía Gabriela; Bilotas, Mariela Andrea; Alaniz, Laura; Barañao, Rosa Inés; Meresman, Gabriela Fabiana
• Is Part Of: European journal of clinical investigation. Volume 53:Number 3(2023)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2022-11-16
• Subjects: 4‐methylumbelliferone -- endometrial cells -- endometriosis -- hyaluronic acid; Pathology -- Periodicals; Medical research -- Periodicals; 616.075
• DOI: 10.1111/eci.13899
• Languages: English
• ISSNs: 0014-2972

Abstract

Abstract: Background: Dysregulated hyaluronic acid (HA) metabolism has been shown to be implicated in several pathologies including endometriosis. 4‐Methylumbelliferone (4MU) is an HA synthesis inhibitor with proven antitumour activity. In this study, we aim to evaluate the effect of 4MU on endometriosis development both in vivo and in vitro. Methods: Endometriosis was surgically induced by uterine tissue auto‐transplantation in 32 two‐month‐old BALB/c mice. Animals were designated into the early or late starting treatment group, which initiated on day 2 or day 15 after surgery, respectively. Within each group, 4MU 200 mg/kg/day or vehicle (Control) were administered by oesophageal gavage for 28 days. After sacrifice, the percentage of developed lesions, lesion size, cell proliferation, vascularization and HA deposition within the endometriotic‐like lesions were evaluated. Cell viability was assessed in endometrial epithelial cells (ECC‐1) and in endometrial stromal cells (t‐HESC); and migration was evaluated in t‐HESC. Results: There was a significant reduction in the percentage of developed lesions in mice that started the 4MU treatment on day 2 compared with its respective control group, and compared with those that started treatment on day 15. However, no significant changes were found when analysing endometriotic‐like lesion's cell proliferation, vascularization and HA deposition. In vitro, both cell viability and migration were inhibited by 4MU treatment. Conclusions: The inhibition of HA synthesis could be a beneficial and alternative option to treat endometriosis at the early stage of the disease. Further research is necessary to elucidate 4MU's mechanism of action and better strategies for delivering this promising drug.