Snail1 Expression Is Required for Sarcomagenesis

Lorena Alba-Castellón, Raquel Batlle, Clara Francí, María J. Fernández-Aceñero, Rocco Mazzolini, Raúl Peña, Jordina Loubat, Francesc Alameda, Rufo Rodríguez, Josué Curto, Joan Albanell, Alberto Muñoz, Félix Bonilla, J. Ignacio Casal, Federico Rojo, Antonio García de Herreros

Research output: Contribution to journalArticleResearchpeer-review

20 Citations (Scopus)

Abstract

© 2014. Snail1 transcriptional repressor is a major inducer of epithelial-to mesenchymal transition but is very limitedly expressed in adult animals. We have previously demonstrated that Snail1 is required for the maintenance of mesenchymal stem cells (MSCs), preventing their premature differentiation. Now, we show that Snail1 controls the tumorigenic properties of mesenchymal cells. Increased Snail1 expression provides tumorigenic capabilities to fibroblastic cells; on the contrary, Snail1 depletion decreases tumor growth. Genetic depletion of Snail1 in MSCs that are deficient in p53 tumor suppressor downregulates MSC markers and prevents the capability of these cells to originate sarcomas in immunodeficient SCID mice. Notably, an analysis of human sarcomas shows that, contrarily to epithelial tumors, these neoplasms display high Snail1 expression. This is particularly clear for undifferentiated tumors, which are associated with poor outcome. Together, our results indicate a role for Snail1 in the generation of sarcomas.
Original languageEnglish
Pages (from-to)413-421
JournalNeoplasia
Volume16
Issue number5
DOIs
Publication statusPublished - 1 Jan 2014

Fingerprint Dive into the research topics of 'Snail1 Expression Is Required for Sarcomagenesis'. Together they form a unique fingerprint.

  • Cite this

    Alba-Castellón, L., Batlle, R., Francí, C., Fernández-Aceñero, M. J., Mazzolini, R., Peña, R., Loubat, J., Alameda, F., Rodríguez, R., Curto, J., Albanell, J., Muñoz, A., Bonilla, F., Ignacio Casal, J., Rojo, F., & García de Herreros, A. (2014). Snail1 Expression Is Required for Sarcomagenesis. Neoplasia, 16(5), 413-421. https://doi.org/10.1016/j.neo.2014.05.002