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Updated: Sep 30, 2025

Induction of Mesenchymal-Epithelial Transitions in Sarcoma Cells
Published on: April 7, 2017
Transcriptional and post-transcriptional control of epithelial-mesenchymal plasticity: why so many regulators?
Melodie Migault1, Sunil Sapkota1, Cameron P Bracken2,3,4
1Gene Regulatory Networks Laboratory, Centre for Cancer Biology, an Alliance between the University of South Australia and SA Pathology, Bradley Building, Rm HB-9-31, North Terrace, Adelaide, SA, 5000, Australia.
Abstract:
The dynamic transition between epithelial-like and mesenchymal-like cell states has been a focus for extensive investigation for decades, reflective of the importance of Epithelial-Mesenchymal Transition (EMT) through development, in the adult, and the contributing role EMT has to pathologies including metastasis and fibrosis. Not surprisingly, regulation of the complex genetic networks that underlie EMT have been attributed to multiple transcription factors and microRNAs. What is surprising, however, are the sheer number of different regulators (hundreds of transcription factors and microRNAs) for which critical roles have been described. This review seeks not to collate these studies, but to provide a perspective on the fundamental question of whether it is really feasible that so many regulators play important roles and if so, what does this tell us about EMT and more generally, the genetic machinery that controls complex biological processes.
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