DNA methylation, epimutations and cancer predisposition

被引:52
作者
Dobrovic, Alexander [1 ,2 ]
Kristensen, Lasse S. [1 ,3 ]
机构
[1] Peter MacCallum Canc Ctr, Dept Pathol, Mol Pathol Res & Dev Lab, Melbourne, Vic 8006, Australia
[2] Univ Melbourne, Dept Pathol, Melbourne, Vic 3010, Australia
[3] Univ Aarhus, Inst Human Genet, DK-8000 Aarhus C, Denmark
基金
英国医学研究理事会;
关键词
DNA methylation; Cancer predisposition; Epimutations; Inheritance; Single nucleotide polymorphisms; TUMOR-SUPPRESSOR GENE; NONPOLYPOSIS COLORECTAL-CANCER; HERITABLE GERMLINE EPIMUTATION; BRCA1 PROMOTER METHYLATION; SPORADIC BREAST-CANCER; MICROSATELLITE INSTABILITY; EPIGENETIC INHERITANCE; ESTROGEN-RECEPTOR; OVARIAN-TUMORS; E-CADHERIN;
D O I
10.1016/j.biocel.2008.09.006
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
Hereditary cancer syndromes caused by germline mutations give rise to distinct spectra of cancel's with characteristic clinico-pathological features. Many of these hereditary cancer genes are silenced by methylation in a similar spectrum of sporadic cancers. It is likely that the initiating event in some of those cases of sporadic cancer is the somatic epigenetic inactivation (epimutation) of the same hereditary cancer gene. Recently, it has been shown that epimutations of certain hereditary cancer genes can be constitutional i.e. Present till throughout the soma. These epimutations may be inherited or arise very early in the germline. The heritability of these epimutations is very low as in most cases they are erased by passage through the germline. In other cases, predisposition to epimutations rather than the epimutations themselves call be inherited. These cases are characterised by Mendelian inheritance and are likely to be associated with sequence variants. Other sequence variants and environmental influences may also affect methylation propensity at a global level. Crown Copyright (C) 2008 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:34 / 39
页数:6
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