Downregulation of cylindromatosis gene, CYLD, confers a growth advantage on malignant melanoma cells while negatively regulating their migration activity

Int J Oncol. 2012 Jul;41(1):53-60. doi: 10.3892/ijo.2012.1424. Epub 2012 Apr 2.

Abstract

The cylindromatosis gene (CYLD) encodes a deubiquitinase that was initially identified as a tumor suppressor and has recently been investigated in connection with a variety of normal physiological processes. In contrast to its cell-proliferative activity, the effect of CYLD protein on cell migration has been a matter of debate. We investigated the effect of CYLD-siRNA on the migration activity of malignant melanoma cells. Expression of CYLD mRNA/protein was lower in 6 of 8 malignant melanoma cell lines than in 3 sets of primary-cultured normal human epidermal melanocytes. Knockdown of CYLD significantly increased the proliferation activities of two melanoma cell lines (p<0.05), along with BCL3 nuclear translocation followed by CCND1 overexpression. In contrast to the proliferation-related activity, CYLD knockdown significantly decreased the cell migration of all the melanoma cell lines (n=7, p<0.05), and we demonstrated that the mechanism regulating melanoma cell migration was activation of RAC1 through the action of CYLD. Our findings provide new insight into the role of CYLD-induced RAC1 activation in melanoma cell migration.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylation
  • B-Cell Lymphoma 3 Protein
  • Cell Line, Tumor
  • Cell Movement*
  • Cell Proliferation*
  • Deubiquitinating Enzyme CYLD
  • Down-Regulation*
  • Gene Expression
  • Gene Knockdown Techniques
  • Histone Deacetylase 6
  • Histone Deacetylases / metabolism
  • Humans
  • Lamin Type B / metabolism
  • Melanocytes / metabolism
  • Melanoma / metabolism*
  • Melanoma / pathology
  • Microtubules / metabolism
  • Primary Cell Culture
  • Protein Processing, Post-Translational
  • Proto-Oncogene Proteins / metabolism
  • RNA Interference
  • Skin Neoplasms / metabolism*
  • Skin Neoplasms / pathology
  • Transcription Factors / metabolism
  • Tubulin / metabolism
  • Tumor Suppressor Proteins / genetics*
  • Tumor Suppressor Proteins / metabolism
  • rac1 GTP-Binding Protein / genetics
  • rac1 GTP-Binding Protein / metabolism

Substances

  • B-Cell Lymphoma 3 Protein
  • BCL3 protein, human
  • Lamin Type B
  • Proto-Oncogene Proteins
  • Transcription Factors
  • Tubulin
  • Tumor Suppressor Proteins
  • CYLD protein, human
  • Deubiquitinating Enzyme CYLD
  • HDAC6 protein, human
  • Histone Deacetylase 6
  • Histone Deacetylases
  • rac1 GTP-Binding Protein