p21-Activated Kinase 1 Promotes Breast Tumorigenesis via Phosphorylation and Activation of the Calcium/Calmodulin-Dependent Protein Kinase II
2022
Héctor I. Saldivar-Cerón | Héctor I. Saldivar-Cerón | Olga Villamar-Cruz | Claire M. Wells | Ibrahim Oguz | Federica Spaggiari | Jonathan Chernoff | Genaro Patiño-López | Sara Huerta-Yepez | Mayra Montecillo-Aguado | Clara M. Rivera-Pazos | Marco A. Loza-Mejía | Alonso Vivar-Sierra | Paola Briseño-Díaz | Alejandro Zentella-Dehesa | Alejandro Zentella-Dehesa | Alfonso Leon-Del-Rio | Alejandro López-Saavedra | Laura Padierna-Mota | María de Jesús Ibarra-Sánchez | José Esparza-López | Rosaura Hernández-Rivas | Luis E. Arias-Romero
p21-Activated kinase-1 (Pak1) is frequently overexpressed and/or amplified in human breast cancer and is necessary for transformation of mammary epithelial cells. Here, we show that Pak1 interacts with and phosphorylates the Calcium/Calmodulin-dependent Protein Kinase II (CaMKII), and that pharmacological inhibition or depletion of Pak1 leads to diminished activity of CaMKII. We found a strong correlation between Pak1 and CaMKII expression in human breast cancer samples, and combined inhibition of Pak1 and CaMKII with small-molecule inhibitors was synergistic and induced apoptosis more potently in Her2 positive and triple negative breast cancer (TNBC) cells. Co-adminstration of Pak and CaMKII small-molecule inhibitors resulted in a dramatic reduction of proliferation and an increase in apoptosis in a 3D cell culture setting, as well as an impairment in migration and invasion of TNBC cells. Finally, mice bearing xenografts of TNBC cells showed a significant delay in tumor growth when treated with small-molecule inhibitors of Pak and CaMKII. These data delineate a signaling pathway from Pak1 to CaMKII that is required for efficient proliferation, migration and invasion of mammary epithelial cells, and suggest new therapeutic strategies in breast cancer.
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