Extracellular glutamate activates metabotropic glutamate receptor 3 (mGluR3), and this drives endosomal trafficking of the membrane type 1 matrix metalloproteinase (MT1-MMP) to promote disruption of basement membranes, which contributes to invasiveness, and lung colonization by mammary carcinoma cells is opposed by i.p. administration of a small-molecule inhibitor of mGluR3 (Dornier et al., 2017). This evidence concerns the gene MMP14 and breast carcinoma.