cDNA microarray analysis of genes associated with ERBB2 (HER2/neu) overexpression in human mammary luminal epithelial cells

被引:133
作者
Mackay, A
Jones, C
Dexter, T
Silva, RLA
Bulmer, K
Jones, A
Simpson, P
Harris, RA
Jat, PS
Neville, AM
Reis, LFL
Lakhani, SR
O'Hare, MJ
机构
[1] UCL, LICR UCL Breast Canc Lab, London W1W 7EJ, England
[2] Inst Canc Res, Breakthrough Toby Robins Breast Canc Res Ctr, London SW3 6JB, England
[3] Ludwig Inst Canc Res, Sao Paulo, Brazil
[4] UCL, Ludwig Inst Canc Res, London, England
[5] Royal Marsden Hosp, London SW3 6JJ, England
基金
英国惠康基金;
关键词
ERBB2 (HER2/neu); breast cancer; cDNA microarray; expression profiling; tissue array;
D O I
10.1038/sj.onc.1206349
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To investigate changes in gene expression associated with ERBB2, expression profiting of immortalized human mammary luminal epithelial cells and variants expressing a moderate and high level of ERBB2 has been carried out using cDNA microarrays corresponding to approximately 6000 unique genes/ESTs. A total of 61 significantly up- or downregulated (>2.0-fold) genes were identified and further validated by RT-PCR analysis as well as microarray comparisons with a spontaneously ERBB2-overexpressing breast cancer cell line and ERBB2-positive primary breast tumors. The expression and clinical relevance of proteins predicted to be associated with ERBB2 overexpression in breast cancers were analysed together with their clinical relevance by antibody screening using a tissue array. Differentially regulated genes include those involved in cell-matrix interactions including proline 4-hydroxylase (P4HA2), galectin 1 (LGALS1) and galectin 3 (LGALS3), fibronectin 1 (FN1) and p-cadherin (CDH3), and cell proliferation (CRIP1, IGFBP3) and transformation (S100P, S100A4). A number of genes associated with MYC signalling were also differentially expressed, including NDRG1, USF2 and the epithelial membrane proteins 1 and 3 (EMP1, EMP3). These data represent profiles of the transcriptional changes associated with ERBB2-related pathways in the breast, and identify novel and potentially useful targets for prognosis and therapy.
引用
收藏
页码:2680 / 2688
页数:9
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