lecce.tecnomedpuglia

Abstract

The STORM project aims to investigate the role of the cell secretory pathway in modulating the tumor microenvironment (TME) in pancreatic ductal adenocarcinoma (PDAC). The hypothesis is that extracellular matrix (ECM) stiffness, a mechanical cue, can perpetuate fibrosis by regulating the secretion of key ECM proteins. By combining molecular biology, biochemistry, and imaging approaches, this project will explore the stiffness-induced Regulators Of Protein Secretion (ROPS) as potential druggable targets of PDAC. Deliverables include generating tunable 3D in vitro models, evaluating protein traffic upon stiffness perturbations, and identifying stiffness-sensitive ROPS through phosphoproteomic experiments. Ultimately, the research aims to provide novel therapeutic strategies to reprogram the stiffness of cell-derived ECMs, which is therapeutically desirable as opposed to stromal ablation, the latter proven to be detrimental to patients.

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