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Absence of p300 induces cellular phenotypic changes characteristic of epithelial to mesenchyme transition

  • D. Krubasik
  • , N. G. Iyer
  • , W. R. English
  • , A. A. Ahmed
  • , M. Vias
  • , C. Roskelley
  • , J. D. Brenton
  • , C. Caldas
  • , G. Murphy*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

41 Scopus citations

Abstract

p300 is a transcriptional cofactor and prototype histone acetyltransferase involved in regulating multiple cellular processes. We generated p300 deficient (p300-) cells from the colon carcinoma cell line HCTI16 by gene targeting. Comparison of epithelial and mesenchymal proteins in p300- with parental HCTI16 cells showed that a number of genes involved in cell and extracellular matrix interactions, typical of 'epithelial to mesenchyme transition' were differentially regulated at both the RNA and protein level. p300- cells were found to have aggressive 'cancer' phenotypes, with loss of cell-cell adhesion, defects in cell-matrix adhesion and increased migration through collagen and matrigel. Although migration was shown to be metalloproteinase mediated, these cells actually showed a downregulation or no change in the level of key metalloproteinases, indicating that changes in cellular adhesion properties can be critical for cellular mobility.

Original languageEnglish
Pages (from-to)1326-1332
Number of pages7
JournalBritish Journal of Cancer
Volume94
Issue number9
DOIs
StatePublished - 8 May 2006
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • E-cadherin
  • HCTI16
  • Homologous recombination
  • p300

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