Periodic Reporting for period 2 - TRENDO (Translational Research on Endometriosis)
Berichtszeitraum: 2023-08-01 bis 2025-07-31
In WP2, TRENDO developed a novel 3D model of endometriosis comprising epithelial and stroma cells that reflects separate extracellular matrix constituents of stroma and epithelium. The impact of cytokines dysregulated in endometriosis on the window of implantation as a fertility-associated readout of endometriosis was studied using trophoblastoid cell lines, guided by our transcriptomic data. The impact of endometriotic organoids on neurons as a readout of pain-related parameters of endometriosis,was demonstrated using carnosic acid treatment, demonstrating its possible suitability for reducing pain associated neuronal growth in vitro.
In WP3, we explored the application of homing peptides for precision delivery of diagnostic and therapeutic compounds to endometriotic lesions. Silver nanoparticles functionalized with synthetic PL1 peptide showed specific internalization endometriotic cells. PL1-nanoparticles loaded with antimitotic monomethyl auristatin E decreased the viability of endometriotic cells and specifically bound to the cryosections of clinical peritoneal endometriotic lesions in the areas positive for TNC-C and Fn-EDB.
In WP4, we revealed higher levels of 2-hydroxy 3-methoxy estrone (2OH, 3MeO-E1) in serum samples of endometriosis patients compared to controls. Higher metabolite levels were linked to an increased endometriosis risk, representing 2OH, 3MeO-E1 as potential adverse markers. In addition, we tested natural therapies for endometriosis, including rosemary extract / carnosic acid as a promising compound in multiple experimental models.