During such a reversion, cancer cells re-express several previously repressed genes, including those involved in cell plasticity (Oct4, SOX-2, and Nanog), while genes (PSEN1, Notch-1) and proteins (SNAI1, αSMA, N-cadherin) supporting epithelial–mesenchymal transition (EMT) are downregulated [38]. Here, POU5F1 is linked to cancer.