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

被引:43
作者
Krubasik, D
Iyer, NG
English, WR
Ahmed, AA
Vias, M
Roskelley, C
Brenton, JD
Caldas, C
Murphy, G
机构
[1] Univ Cambridge, Addenbrookes Hosp, Med Res Inst, Dept Oncol, Cambridge CB2 2XY, England
[2] Univ Cambridge, MRC, Res Ctr, Dept Oncol,Canc Genom Program, Cambridge CB2 2XZ, England
[3] Univ British Columbia, Dept Anat, Vancouver, BC V6T 1Z3, Canada
关键词
p300; HCT116; homologous recombination; e-cadherin;
D O I
10.1038/sj.bjc.6603101
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:1326 / 1332
页数:7
相关论文
共 20 条
[1]   Microarray segmentation methods significantly influence data precision [J].
Ahmed, AA ;
Vias, M ;
Iyer, NG ;
Caldas, C ;
Brenton, JD .
NUCLEIC ACIDS RESEARCH, 2004, 32 (05) :e50
[2]   Invasion and metastasis in colorectal cancer:: Epithelial-mesenchymal transition, mesenchymal-epithelial transition, stem cells and β-catenin [J].
Brabletz, T ;
Hlubek, F ;
Spaderna, S ;
Schmalhofer, O ;
Hiendlmeyer, E ;
Jung, A ;
Kirchner, T .
CELLS TISSUES ORGANS, 2005, 179 (1-2) :56-65
[3]  
Chan HM, 2001, J CELL SCI, V114, P2363
[4]   The PEA3 subfamily of Ets transcription factors synergizes with β-catenin-LEF-1 to activate matrilysin transcription in intestinal tumors [J].
Crawford, HC ;
Fingleton, B ;
Gustavson, MD ;
Kurpios, N ;
Wagenaar, RA ;
Hassell, JA ;
Matrisian, LM .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (04) :1370-1383
[5]   Review - Proteases, extracellular matrix, and cancer - A workshop of the path B study section [J].
DeClerck, YA ;
Mercurio, AM ;
Stack, MS ;
Chapman, HA ;
Zutter, MM ;
Muschel, RJ ;
Raz, A ;
Matrisian, LM ;
Sloane, BF ;
Noel, A ;
Hendrix, MJ ;
Coussens, L ;
Padarathsingh, M .
AMERICAN JOURNAL OF PATHOLOGY, 2004, 164 (04) :1131-1139
[6]   Mutations truncating the EP300 acetylase in human cancers [J].
Gayther, SA ;
Batley, SJ ;
Linger, L ;
Bannister, A ;
Thorpe, K ;
Chin, SF ;
Daigo, Y ;
Russell, P ;
Wilson, A ;
Sowter, HM ;
Delhanty, JDA ;
Ponder, BAJ ;
Kouzarides, T ;
Caldas, C .
NATURE GENETICS, 2000, 24 (03) :300-303
[7]  
Goodman RH, 2000, GENE DEV, V14, P1553
[8]   P300 regulates p53-dependent apoptosis after DNA damage in colorectal cancer cells by modulation of PUMA/p21 levels [J].
Iyer, NG ;
Chin, SF ;
Ozdag, H ;
Daigo, Y ;
Hu, DE ;
Cariati, M ;
Brindle, K ;
Aparicio, S ;
Caldas, C .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (19) :7386-7391
[9]   p300/CBP and cancer [J].
Iyer, NG ;
Özdag, H ;
Caldas, C .
ONCOGENE, 2004, 23 (24) :4225-4231
[10]   The modulation of matrix metalloproteinase and ADAM gene expression in human chondrocytes by interleukin-1 and oncostatin M - A time-course study using real-time quantitative reverse transcription-polymerase chain reaction [J].
Koshy, PJT ;
Lundy, CJ ;
Rowan, AD ;
Porter, S ;
Edwards, DR ;
Hogan, A ;
Clark, IM ;
Cawston, TE .
ARTHRITIS AND RHEUMATISM, 2002, 46 (04) :961-967