Calcium sensing receptor stimulates breast cancer cell migration via the Gβγ-AKT-mTORC2 signaling pathway
Lennis B. Orduña-Castillo, Jorge Eduardo del-Río-Robles, Irving García‐Jiménez, César Zavala-Barrera, Yarely Mabell Beltrán‐Navarro, Joseline Janai Hidalgo‐Moyle, Iliana Ramírez-Rangel, Marco Antonio Hernández-Bedolla, Alma P. Reyes-Ibarra, Margarita Valadez-Sánchez, José Vázquez‐Prado, Guadalupe Reyes‐Cruz
Abstract
Calcium sensing receptor, a pleiotropic G protein coupled receptor, activates secretory pathways in cancer cells and putatively exacerbates their metastatic behavior. Here, we show that various CaSR mutants, identified in breast cancer patients, differ in their ability to stimulate Rac, a small Rho GTPase linked to cytoskeletal reorganization and cell protrusion, but are similarly active on the mitogenic ERK pathway. To investigate how CaSR activates Rac and drives cell migration, we used invasive MDA-MB-231 breast cancer cells. We revealed, by pharmacological and knockdown strategies, that CaSR activates Rac and cell migration via the Gβγ-PI3K-mTORC2 pathway. These findings further support current efforts to validate CaSR as a relevant therapeutic target in metastatic cancer.