Several reports have shown that members of the miR-200 family (miR-200a,b,c, miR-141 and miR-429) inhibit epithelial mesenchymal transition (EMT) through direct targeting of ZEB1 and ZEB2, which encode transcriptional repressors of E-cadherin in kidney tubular cells[4], breast cancer cells[5], and mammary epithelial cells[3]. This evidence concerns the gene ZEB2 and breast carcinoma.