Constitutional Mosaic Epimutations - a hidden cause of cancer?
Ontology highlight
ABSTRACT: Silencing of tumor suppressor genes by promoter hypermethylation is a key mechanism to facilitate cancer progression in many malignancies. While promoter hypermethylation can occur at later stages of the carcinogenesis process, constitutional methylation of key tumor suppressors may be an initiating event whereby cancer is started. Constitutional BRCA1 methylation due to cis-acting germline genetic variants is associated with a high risk of breast and ovarian cancer. However, this seems to be a rare event, restricted to a very limited number of families. In contrast, mosaic constitutional BRCA1 methylation is detected in 4-7% of newborn females without germline BRCA1 mutations. While the cause of such methylation is poorly understood, mosaic normal tissue BRC
SUBMITTER: Lonning PE
PROVIDER: S-EPMC6551830 | biostudies-literature | 2019 Mar
REPOSITORIES: biostudies-literature
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