Abstract 2859: Targeting the calcium sensing receptor in breast cancer cells diminishes colonization and migratory response in a trabecular bone explant model, and reduces osteolytic lesions in vivo

Breast cancer is the most common form of cancer affecting women worldwide with bones being the prevalent site of metastasis. The calcium sensing receptor (CaSR), whose primary physiological role is calcium homeostasis, has emerged as a new target in the “vicious cycle” that amplifies the metastatic cascade. Our team had already shown that overexpression of the CaSR dramatically increased the osteolytic potential of MDA-MB-231 cells in vivo. Our objective here was to study the involvement of CaSR in the metastasis of breast cancer cells to the bone using human femur tissue explants and to abate it with calcilytics (CaSR antagonists). Methods: To investigate the role of CaSR in migration of breast cancer cells, MDA-MB-231 cells were made to overexpress either a full-length wild-type CaSR (CaSR-WT) or a dominant negative mutant (CaSR-DN). For control, cells were transfected with empty pcDNA™3.1/Zeo(+) plasmid (CaSR-EV). NPS 2143 was used as a calcilytic in relevant assays. ERK phosphorylation was checked across all cell types in response to calcium. Trabecular bone fragments, extracted from human femoral heads, were used as explants to study the osteoinvasion in vitro. Transwell inserts seeded with the transfected cells were exposed to the bone fragment supernatant before quantifying migration. Treated/untreated cells were seeded directly onto the bone fragments, and zeocin-selective colony formation assay was performed with the extracted marrow population. Mice were inoculated intra-tibially with MDA-B02 cells and received NPS-2143 (IP) for 7 days. Results: The cultured supernatant elicited a strong migratory response across all transfected cell types. In these culture conditions, the CaSR-WT and CaSR-EV cells had a 50% increase in migration levels over the CaSR-DN (p