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 language | English |
|---|---|
| Pages (from-to) | 1326-1332 |
| Number of pages | 7 |
| Journal | British Journal of Cancer |
| Volume | 94 |
| Issue number | 9 |
| DOIs | |
| State | Published - 8 May 2006 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- E-cadherin
- HCTI16
- Homologous recombination
- p300
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