c-Cbl regulates αPix-mediated cell migration and invasion

Biochem Biophys Res Commun. 2014 Dec 12;455(3-4):153-8. doi: 10.1016/j.bbrc.2014.10.129. Epub 2014 Nov 1.

Abstract

c-Cbl, a RING-type ubiquitin E3 ligase, down-regulates receptor tyrosine kinases, including EGF receptor, and inhibits cell proliferation. Moreover, c-Cbl mutations are frequently found in patients with myeloid neoplasm. Therefore, c-Cbl is known as a tumor suppressor. αPix is expressed only in highly proliferative and mobile cells, including immune cells, and up-regulated in certain invasive tumors, such as glioblastoma multiforme. Here, we showed that c-Cbl serves as an ubiquitin E3 ligase for proteasome-mediated degradation of αPix, but not βPix. Remarkably, the rat C6 and human A172 glioma cells were unable to express c-Cbl, which leads to a dramatic accumulation of αPix. Depletion of αPix by shRNA markedly reduced the ability of the glioma cells to migrate and invade, whereas complementation of shRNA-insensitive αPix promoted it. These results indicate that c-Cbl negatively regulates αPix-mediated cell migration and invasion and the lack of c-Cbl in the C6 and A172 glioma cells is responsible for their malignant behavior.

Keywords: Cell invasion; Cell migration; Glioma; c-Cbl; αPix.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Cell Movement
  • ErbB Receptors / metabolism
  • Genetic Complementation Test
  • Glioma / metabolism
  • HEK293 Cells
  • Humans
  • Leukemia, Myeloid / genetics*
  • Leukemia, Myeloid / metabolism
  • Mutation*
  • Neoplasm Invasiveness
  • Proteasome Endopeptidase Complex / metabolism
  • Protein Binding
  • Proto-Oncogene Proteins c-cbl / metabolism*
  • RNA, Messenger / metabolism
  • RNA, Small Interfering / metabolism
  • Rats
  • Rho Guanine Nucleotide Exchange Factors / metabolism
  • Ubiquitin-Protein Ligases / metabolism
  • Up-Regulation

Substances

  • ARHGEF6 protein, human
  • RNA, Messenger
  • RNA, Small Interfering
  • Rho Guanine Nucleotide Exchange Factors
  • Proto-Oncogene Proteins c-cbl
  • Ubiquitin-Protein Ligases
  • ErbB Receptors
  • Proteasome Endopeptidase Complex
  • CBL protein, human