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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

Research output: Contribution to journalArticlepeer-review

41 Citations (Scopus)

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 HCT116 by gene targeting. Comparison of epithelial and mesenchymal proteins in p300− with parental HCT116 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
Publication statusPublished - 18 Apr 2006

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

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