4.7 Article

Tumor-Stromal Interactions in a Co-Culture Model of Human Pancreatic Adenocarcinoma Cells and Fibroblasts and Their Connection with Tumor Spread

Journal

BIOMEDICINES
Volume 9, Issue 4, Pages -

Publisher

MDPI
DOI: 10.3390/biomedicines9040364

Keywords

pancreatic ductal adenocarcinoma; cancer-associated fibroblasts; cocultures; cytokines; extracellular vesicles

Funding

  1. Fundacion Medica Mutua Madrilena [06/0137]

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Researchers found in an in vitro coculture model that under coculture conditions, fibroblasts were activated, epithelial markers in tumor cells were decreased, and the two types of cells migrated together. Changes in IL-6 levels could potentially affect the invasive and migratory capacities of the cells. Targeting the interaction between tumor cells and the tumor microenvironment could be a novel therapeutic approach for advanced PDAC.
One key feature of pancreatic ductal adenocarcinoma (PDAC) is a dense desmoplastic reaction that has been recognized as playing important roles in metastasis and therapeutic resistance. We aim to study tumor-stromal interactions in an in vitro coculture model between human PDAC cells (Capan-1 or PL-45) and fibroblasts (LC5). Confocal immunofluorescence, Enzyme-Linked Immunosorbent Assay (ELISA), and Western blotting were used to evaluate the expressions of activation markers; cytokines arrays were performed to identify secretome profiles associated with migratory and invasive properties of tumor cells; extracellular vesicle production was examined by ELISA and transmission electron microscopy. Coculture conditions increased FGF-7 secretion and alpha-SMA expression, characterized by fibroblast activation and decreased epithelial marker E-cadherin in tumor cells. Interestingly, tumor cells and fibroblasts migrate together, with tumor cells in forming a center surrounded by fibroblasts, maximizing the contact between cells. We show a different mechanism for tumor spread through a cooperative migration between tumor cells and activated fibroblasts. Furthermore, IL-6 levels change significantly in coculture conditions, and this could affect the invasive and migratory capacities of cells. Targeting the interaction between tumor cells and the tumor microenvironment might represent a novel therapeutic approach to advanced PDAC.

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