TGF-β1 acts through miR-155 to down-regulate TP53INP1 in promoting epithelial-mesenchymal transition and cancer stem cell phenotypes

Cancer Lett. 2015 Apr 10;359(2):288-98. doi: 10.1016/j.canlet.2015.01.030. Epub 2015 Jan 26.

Abstract

It has been shown that acquisition of epithelial-mesenchymal transition (EMT) and induction of cancer stem cell (CSC)-like properties contribute to metastasis of cancers in many studies; however, the molecular mechanisms underlying EMT and CSC phenotypes in liver cancer cells remain to be elucidated. MiR-155 is an important microRNA associated with tumour progression. Here, we report that miR-155 regulates not only the epithelial-mesenchymal transition but also the stem-like transition in liver cancer cells. Utilizing quantitative RT-PCR, we found that the expression of miR-155 is positively related to the levels of CD90, CD133 and Oct4 in enriched spheres. Up-regulated miR-155 significantly increases the population of stem-like CSCs among liver cancer cells and the ability to form tumour spheres. Additionally, miR-155 overexpression in cells significantly increases cell motility and invasion, as well as the epithelial-mesenchymal transition process. Conversely, suppression of miR-155 in cells had an opposite effect, which was partially rescued by the down-regulation of TP53INP1. Collectively, miR-155 promotes liver cancer cell EMT and CSCs, in part, via silencing TP53INP1. In addition, we found that TGF-β1 indirectly regulates TP53INP1 expression via miR-155 in liver cancer cells. Taken together, our findings suggest that miR-155 regulates TP53INP1 expression, to induce the epithelial-mesenchymal transition and acquisition of a stem cell phenotype.

Keywords: Cancer stem cell; Epithelial–mesenchymal transition; MiR-155; TP53INP1; Tumour sphere.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carrier Proteins / genetics*
  • Carrier Proteins / metabolism
  • Epithelial-Mesenchymal Transition*
  • Gene Expression
  • Heat-Shock Proteins / genetics*
  • Heat-Shock Proteins / metabolism
  • Hep G2 Cells
  • Humans
  • Liver Neoplasms
  • MicroRNAs / physiology*
  • Neoplastic Stem Cells / metabolism*
  • Phenotype
  • RNA Interference
  • Transforming Growth Factor beta1 / physiology*

Substances

  • Carrier Proteins
  • Heat-Shock Proteins
  • MIRN155 microRNA, human
  • MicroRNAs
  • TGFB1 protein, human
  • TP53INP1 protein, human
  • Transforming Growth Factor beta1