Open access protocols and data from patient-derived disease models
Efforts within patient-derived disease models at SGC aim to develop open access protocols and data from well-characterized human disease tissue, blood-derived assays and other model systems to profile chemical probes and chemogenomic libraries, guiding the identification of biomarkers and novel targets to drive drug discovery.
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We focus on areas of high medical need in inflammatory diseases, fibrosis, oncology and neurodegenerative diseases. Specifically, our aim is to define and validate under-explored protein targets by profiling high-quality chemical and antibody probes in patient-derived cell assays of translational value, providing biomarkers, target engagement and phenotypic read-outs using disease-relevant models, including new complex cell co-culture systems.
IMI-funded EUbOPEN project
Our current network of collaborations consists of hospitals, research institutes and universities in Toronto and Montreal (Canada), Frankfurt (Germany) and Stockholm (Sweden). We also collaborate with a number of industrial partners to ensure the high relevance of our models and assays for translational medical studies to support early drug discovery efforts.
In the IMI-funded EUbOPEN project, we have profiled a number of chemical probes and chemogenomic compounds in colorectal cancer, multiple sclerosis and non-alcoholic fatty liver disease (NASH).
IMI-funded ULTRA-DD project
As part of the past IMI-funded ULTRA-DD project, focusing on autoimmune and inflammatory conditions, we identified new targets for disease modulation in systemic lupus erythematosus, myositis, systemic sclerosis, ankylosing spondylitis and Dupuytren’s disease (hand fibrosis).