Methylation of the adenomatous polyposis coli (APC) gene in human placenta and hypermethylation in choriocarcinoma cells

被引:59
作者
Wong, N. C. [1 ,2 ]
Novakovic, B. [1 ]
Weinrich, B. [1 ]
Dewi, C. [1 ]
Andronikos, R. [1 ]
Sibson, M. [1 ]
Macrae, F. [3 ]
Morley, R. [1 ,2 ]
Pertile, M. D. [4 ]
Craig, J. M. [1 ,2 ]
Saffery, R. [1 ,2 ]
机构
[1] Royal Childrens Hosp, Murdoch Childrens Res Inst, Melbourne, Vic 3052, Australia
[2] Univ Melbourne, Dept Paediat, Melbourne, Vic 3010, Australia
[3] Royal Melbourne Hosp, Dept Colorectal Med & Genet, Melbourne, Vic, Australia
[4] Royal Childrens Hosp, Genet Hlth Serv Victoria, Parkville, Vic 3052, Australia
基金
英国医学研究理事会;
关键词
epigenetics; tumour suppressor; adenamatous polyposis coli; placenta; methylation;
D O I
10.1016/j.canlet.2008.03.033
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Methylation of the human APC gene promoter is associated with several different types of cancers and has also been documented in some pre-cancerous tissues. We have examined the methylation of APC gene promoters in human placenta and choriocarcinoma cells. This revealed a general hypomethylation of the APC-1b promoter and a pattern with monoallelic methylation of the APC-1a promoter in full term placental tissue. However, there was no evidence of a parent-of-origin effect, suggesting random post zygotic origin of methylation. Increased methylation of this promoter was observed in all choriocarcinoma-derived trophoblast cell lines, suggesting a trophoblastic origin of placental APC methylation and implicating APC hypermethylation in the development of this group of gestational tumours. Our demonstration of placental methylation of the APC-1a promoter represents the first observation of monoallelic methylation of this gene in early development, and provides further support for a role of canonical Wnt signalling in placental trophoblast invasiveness. This also implicates tumour suppressor gene silencing as an integral part of normal human placental development. (C) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:56 / 62
页数:7
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