Signaling between transforming growth factor β (TGF-β) and transcription factor SNAI2 represses expression of microRNA miR-203 to promote epithelial-mesenchymal transition and tumor metastasis.

Ding X, Park SI, McCauley LK, Wang CY
J Biol Chem. 2013 288 (15): 10241-53

PMID: 23447531 · PMCID: PMC3624408 · DOI:10.1074/jbc.M112.443655

TGF-β promotes tumor invasion and metastasis by inducing an epithelial-mesenchymal transition (EMT). Understanding the molecular and epigenetic mechanisms by which TGF-β induces EMT may facilitate the development of new therapeutic strategies for metastasis. Here, we report that TGF-β induced SNAI2 to promote EMT by repressing miR-203. Although miR-203 targeted SNAI2, SNAI2 induced by TGF-β could directly bind to the miR-203 promoter to inhibit its transcription. SNAI2 and miR-203 formed a double negative feedback loop to inhibit each other's expression, thereby controlling EMT. Moreover, we found that miR-203 was significantly down-regulated in highly metastatic breast cancer cells. The restoration of miR-203 in highly metastatic breast cancer cells inhibited tumor cell invasion in vitro and lung metastatic colonization in vivo by repressing SNAI2. Taken together, our results suggest that the SNAI2 and miR-203 regulatory loop plays important roles in EMT and tumor metastasis.

MeSH Terms (16)

Animals Breast Neoplasms Cell Line, Tumor Dogs Epithelial-Mesenchymal Transition Female Gene Expression Regulation, Neoplastic Humans MicroRNAs Neoplasm Metastasis Neoplasm Proteins RNA, Neoplasm Signal Transduction Snail Family Transcription Factors Transcription Factors Transforming Growth Factor beta

Connections (1)

This publication is referenced by other Labnodes entities: