We have formerly shown that P-cadherin-induced invasion is mediated by the secretion of metalloproteases (MMP1/2) to the extracellular media, which will cleave the complete-size P-cadherin, building a soluble fragment of this protein (sP-cad) with pro-invasive action [6]
MCF-7/AZ.Mock and MCF/AZ.Pcad have been addressed with fifty mM and one hundred mM for 48 h, and offered a decrease in P-cadherin protein ranges, even though E-cadherin ranges have been…