Periodic Reporting for period 1 - TRENDO (Translational Research on Endometriosis)
Berichtszeitraum: 2021-08-01 bis 2023-07-31
The aim of WP2 is the functional characterisation of biomarkers for preclinical testing of drugs by modelling of endometriosis. 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.
The aim of WP3 is the development of novel theranostic solutions for imaging and treatment of endometriosis. 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.
The aim of WP4 is the evaluation of Innovative therapeutics and novel treatments. We have adapted an sCD44 assay to endometriotic samples and performed a pilot study to measure levels of specific set of 16 estrogen metabolites in 209 patients with endometriosis and 115 control patients, revealing 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. The study showed that 2OH pathway is associated with ovarian endometriotic lesions and unfavorable pain outcomes.