The potential role of regulator of G-protein signaling 16 in cell motility mediated by δEF1 family proteins

FEBS Lett. 2016 Jan;590(2):270-8. doi: 10.1002/1873-3468.12042. Epub 2016 Jan 27.

Abstract

The epithelial-mesenchymal transition (EMT) is associated with tumor progression. We reported previously that expression of the δEF1 family proteins (δEF1/ZEB1 and SIP1/ZEB2), key regulators of the EMT, is positively correlated with EMT phenotypes and aggressiveness of breast cancer. Here, we show that the expression levels of regulator of G-protein signaling 16 (RGS16) are negatively correlated with those of the δEF1 family proteins. On the basis of the results of gain- and loss-of-function analyses, we suggest that δEF1 family proteins promote cell motility of breast cancer cells directly or indirectly through repressing expression of RGS16.

Keywords: epithelial-mesenchymal transition; regulator of G-protein signaling 16; smad-interacting protein 1; δEF1; δEF1 family proteins.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Breast Neoplasms / pathology
  • Cell Line, Tumor
  • Cell Movement / physiology*
  • Epithelial-Mesenchymal Transition / physiology
  • Homeodomain Proteins / physiology*
  • Humans
  • RGS Proteins / physiology*
  • Repressor Proteins / physiology*
  • Transcription Factors / physiology*
  • Zinc Finger E-box Binding Homeobox 2
  • Zinc Finger E-box-Binding Homeobox 1

Substances

  • Homeodomain Proteins
  • RGS Proteins
  • RGS16 protein
  • Repressor Proteins
  • Transcription Factors
  • ZEB1 protein, human
  • ZEB2 protein, human
  • Zinc Finger E-box Binding Homeobox 2
  • Zinc Finger E-box-Binding Homeobox 1