4.4 Review

The emerging role of Snail1 in the tumor stroma

Journal

CLINICAL & TRANSLATIONAL ONCOLOGY
Volume 18, Issue 9, Pages 872-877

Publisher

SPRINGER INTERNATIONAL PUBLISHING AG
DOI: 10.1007/s12094-015-1474-9

Keywords

Snail1; Cancer microenvironment; Cancer-associated fibroblasts; Extracellular matrix; Stem cells; Paracrine signals

Categories

Funding

  1. Instituto de Salud Carlos III-FEDER [PI12/02037, RD12/0036/0041]
  2. Fundacion Cientifica AECC
  3. Ministerio de Economia y Competitividad of Spain-FEDER [SAF2010-20750]
  4. Comunidad de Madrid [S2010/BMD-2344]
  5. Fundacion Banco Santander
  6. Instituto de Salud Carlos III

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The transcription factor Snail1 leads to the epithelial-mesenchymal transition by repressing the adherent and tight junctions in epithelial cells. This process is related to an increase of cell migratory and mesenchymal properties during both embryonic development and tumor progression. Although Snail1 expression is very limited in adult animals, emerging evidence has placed Snail at the forefront of medical science. As a transcriptional repressor, Snail1 confers cancer stem cell-like traits on tumor cells and promotes drug resistance, tumor recurrence and metastasis. In this review, we summarize recent reports that suggest the pro-tumorigenic roles of Snail1 expression in tumor stroma. The crosstalk between tumor and stromal cells mediated by Snail1 regulates paracrine communication, pro-tumorigenic abilities of cancer cells, extracellular matrix characteristics and mesenchymal differentiation in cancer stem cells and cancer-associated fibroblasts. Therefore, understanding the regulation and functional roles of Snail1 in the tumor microenvironment will provide us with new therapies for treating metastatic disease.

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