Hyaluronic acid carrier-cell interactions: a tri-culture model of the tumour microenvironment to study siRNA delivery under flow conditions. (19th August 2019)

• Record Type: Journal Article
• Authors: Rosa, Julio M. Rios De La; Tirelli, Nicola; Tirella, Annalisa
• Is Part Of: International journal of nano and biomaterials. Volume 8:Number 2(2019)
• Page Start: 106
• Page End: 117
• Publication Date: 2019-08-19
• Subjects: hyaluronic acid -- CD44 -- tumour microenvironment -- pancreatic cancer -- macrophages -- tumour-associated fibroblasts -- nanoparticle -- targeted drug delivery -- siRNA; Nanostructured materials -- Periodicals; Nanotechnology -- Periodicals; Biomedical materials -- Periodicals; 620.505
• Languages: English
• ISSNs: 1752-8933

Abstract

CD44 is often over expressed in solid tumours, rendering this protein a 'hot' target in drug delivery. As CD44 is the main surface receptor of hyaluronic acid (HA), one of the most common therapeutic approaches consists of hijacking the cell's mechanism of HA endocytosis to deliver active principles. This approach, however, presents two caveats: the poor understanding of HA-cell interactions and the ubiquitous expression of CD44 in other cell types, e.g., stromal cells. To predict the interaction of HA-decorated nanocarriers with CD44-expressing cells in the multi-cellular and complex tumour microenvironment, we have established a tri-culture, non-contact in vitro model (PANC-1 tumoural cells, HDF stromal cells, THP-1 macrophages) and quantified the delivery and kinetics of nanoparticle internalisation (via flow cytometry), investigating the system in both static and dynamic culturing conditions. We report that HA-decorated nanocarriers are able to preferentially deliver siRNA to pancreatic cancer cells, interestingly even under flow/dynamic conditions.