GLI1-dependent transcriptional repression of CYLD in basal cell carcinoma

Oncogene. 2011 Nov 3;30(44):4523-30. doi: 10.1038/onc.2011.163. Epub 2011 May 16.

Abstract

CYLD is a deubiquitination enzyme that regulates different cellular processes, such as cell proliferation and cell survival. Mutation and loss of heterozygosity of the CYLD gene causes development of cylindromatosis, a benign tumour originating from the skin. Our study shows that CYLD expression is dramatically downregulated in basal cell carcinoma (BCC), the most common cancer in humans. Reduced CYLD expression in basal cell carcinoma was mediated by GLI1-dependent activation of the transcriptional repressor Snail. Inhibition of GLI1 restored the CYLD expression-mediated Snail signaling pathway, and caused a significant delay in the G1 to S phase transition, as well as proliferation. Our data suggest that GLI1-mediated suppression of CYLD has a significant role in basal cell carcinoma progression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carcinoma, Basal Cell / genetics
  • Cell Cycle
  • Cell Line, Tumor
  • Cell Proliferation
  • Deubiquitinating Enzyme CYLD
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Skin Neoplasms / genetics
  • Snail Family Transcription Factors
  • Transcription Factors / genetics*
  • Tumor Suppressor Proteins / genetics*
  • Zinc Finger Protein GLI1

Substances

  • GLI1 protein, human
  • Snail Family Transcription Factors
  • Transcription Factors
  • Tumor Suppressor Proteins
  • Zinc Finger Protein GLI1
  • CYLD protein, human
  • Deubiquitinating Enzyme CYLD