Multiple ways of silencing E-cadherin gene expression in lobular carcinoma of the breast

被引:180
作者
Droufakou, S
Deshmane, V
Roylance, R
Hanby, A
Tomlinson, I
Hart, IR [1 ]
机构
[1] St Thomas Hosp, Imperial Canc Res Fund Lab, Rayne Inst, Richard Dimbleby Dept Canc Res, London SE1 7EH, England
[2] Imperial Canc Res Fund, Human Cytogenet Lab, London, England
[3] Imperial Canc Res Fund, Mol & Populat Genet Lab, London WC2A 3PX, England
关键词
breast lobular carcinoma; E-cadherin; LOH; promoter methylation;
D O I
10.1002/ijc.1208
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The cell-cell adhesion receptor gene E-cadherin (CDH1) is expressed by epithelial cells, in which it mediates adhesion and morphogenesis. Invasive lobular carcinoma (ILC) characteristically infiltrates diffusely as single cells; by immunohistochemistry, many of these tumours lack E-cadherin expression. in the present study we investigated various ways in which loss of function of the E-cadherin gene could occur in ILCs, namely, promoter methylation, mutation and allelic loss. We analysed 22 ILCs and found 12 (55%) E-cadherin-negative samples by immunohistochemical analysis. Methylation-specific polymerase chain reaction (PCR) showed that 17/22 (77%) of these rumours had methylation of the CDH1 promoter, including 11/12 (91%) of the E-cadherin-negative tumours, All 16 exons of E-cadherin (including intron-exon boundaries) were amplified from chromosomal DNA and screened for mutations by conformation-sensitive gel electrophoresis (CSGE), Bands with altered mobility were analysed by direct sequencing. We identified five frameshift mutations, which resulted in downstream stop codons and one splice site mutation in six different tumours (29%). Loss of heterozygosity (LOH) was assessed using microsatellite markers, and 9/18 (50%) informative tumours showed LOH, We conclude that most ILCs show genetic or epigenetic changes affecting the E-cadherin gene and that many of these tumours lack E-cadherin expression. In all cases in which there was loss of expression, this was consistent with biallelic inactivation of CDH1 by promoter methylation, mutation or allelic loss in any combination. (C) 2001 Wiley-Liss. Inc.
引用
收藏
页码:404 / 408
页数:5
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