The Snail family of transcription factors has previously been implicated in
the differentiation of epithelial cells into mesenchymal cells (epithelial
-mesenchymal transitions) during embryonic development. Epithelial-mesenchy
mal transitions are also determinants of the progression of carcinomas, occ
urring concomitantly with the cellular acquisition of migratory properties
following downregulation of expression of the adhesion protein E-cadherin.
Here we show that mouse Snail is a strong repressor of transcription of the
E-cadherin gene. Epithelial cells that ectopically express Snail adopt a f
ibroblastoid phenotype and acquire tumorigenic and invasive properties. End
ogenous Snail protein is present in invasive mouse and human carcinoma cell
lines and tumours in which E-cadherin expression has been lost. Therefore,
the same molecules are used to trigger epithelial-mesenchymal transitions
during embryonic development and in tumour progression. Snail may thus be c
onsidered as a marker for malignancy, opening up new avenues for the design
of specific anti-invasive drugs.