Ontology highlight
ABSTRACT: Background
Pancreatic ductal adenocarcinoma (PDAC) is characterized by a dense, hypoxic and immune-suppressive tumor microenvironment (TME). Integrin αvβ3-expressing cells, including endothelial and cancer-associated fibroblasts (CAFs), contribute to the development of this TME. ProAgio is a novel cytotoxin that targets integrin αvβ3-expressing cells. ProAgio is currently in clinical trials. We have previously shown that the combination of GPH (gemcitabine, paricalcitol, and hydroxychloroquine) influences PDAC TME. Based on the overlapping mechanisms of action, we hypothesized that ProAgio could potentiate effects of GPH and enhance its anti-tumor immunity.Methods
Patient-derived xenograft (PDX) and orthotopic models of PDAC were used to assess the therapeutic activity and
SUBMITTER: Bandi DSR
PROVIDER: S-EPMC12871271 | biostudies-literature | 2026 Jan
REPOSITORIES: biostudies-literature