Heritable DNA methylation marks associated with susceptibility to breast cancer
Details
Publication Year 2018-02-28,Volume 9,Issue #1,Page 867
Journal Title
Nature Communications
Publication Type
Journal Article
Abstract
Mendelian-like inheritance of germline DNA methylation in cancer susceptibility genes has been previously reported. We aimed to scan the genome for heritable methylation marks associated with breast cancer susceptibility by studying 25 Australian multiple-case breast cancer families. Here we report genome-wide DNA methylation measured in 210 peripheral blood DNA samples provided by family members using the Infinium HumanMethylation450. We develop and apply a new statistical method to identify heritable methylation marks based on complex segregation analysis. We estimate carrier probabilities for the 1000 most heritable methylation marks based on family structure, and we use Cox proportional hazards survival analysis to identify 24 methylation marks with corresponding carrier probabilities significantly associated with breast cancer. We replicate an association with breast cancer risk for four of the 24 marks using an independent nested case-control study. Here, we report a novel approach for identifying heritable DNA methylation marks associated with breast cancer risk.
Publisher
Springer Nature
Keywords
Australia; Breast Neoplasms/*genetics/metabolism; Case-Control Studies; Cohort Studies; CpG Islands; *DNA Methylation; Epigenesis, Genetic; Female; Genetic Predisposition to Disease; Humans
Research Division(s)
Stem Cells And Cancer
PubMed ID
29491469
Open Access at Publisher's Site
https://doi.org/10.1038/s41467-018-03058-6
Terms of Use/Rights Notice
Refer to copyright notice on published article.


Creation Date: 2018-05-18 09:33:25
Last Modified: 2018-06-27 09:43:57
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