Affiliations: Department of Chemical and Materials Engineering, University of Kentucky, Lexington, KY 40506, USA | Center for Biomedical Engineering, University of Kentucky, Lexington, KY 40506, USA | Department of Microbiology and Immunology, University of Kentucky, Lexington, KY 40506, USA
Abstract: The mechanical stimulus of shear stress has to date been neglected when studying the adhesion of cancer cells to the endothelium. Confluent monolayers of endothelial cells were subjected to either 4 or 15 hours of arterial shear stress. Adhesion of nonmetastatic (MCF‐7) and highly metastatic (MDA‐MB‐435) human breast cancer cells was then quantified using a detachment assay carried out inside the parallel plate flow chamber. Four hours of shear stress exposure had no effect on adhesion. However, 15 hours of shear stress exposure led to marked changes in the ability of the endothelial monolayer to bind human breast cancer cells. An increase in adhesive strength was observed for nonmetastatic MCF‐7 cells, while a decrease in adhesive strength was observed for highly metastatic MDA‐MB‐435 cells. Hence, endothelial shear stress stimulation does influence the adhesion of cancer cells to the endothelium and can have different effects on the adhesion of cancer cells with different metastatic potentials. Furthermore, adhesion of nonmetastatic and highly metastatic human breast cancer cells may be controlled by two different endothelial cell adhesion molecules that are differentially regulated by shear stress. Immunohistochemistry confirmed that shear stress did in fact differentially regulate endothelial cell adhesion molecule expression.
