Knight et al. have developed a mouse model that resembles the claudin-low subtype of triple-negative breast cancer (TNBC) by expressing a weakly oncogenic MET receptor tyrosine kinase under the control of the mouse mammary tumour virus promoter concomitant with conditionally deleting Trp53 in the mammary gland. Tumours in these mice have a similar molecular signature to human claudin-low TNBC, and require MET for proliferation and for maintaining the claudin-low morphological phenotype. Therefore, MET inhibitors may be effective against TNBC.