Publication: Aging, methylation and cancer
Authors
Ahuja, N. ; Issa, J.-P.J.
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Publisher
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DOI
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info:eu-repo/semantics/article
Description
Abstract
Alterations in methylation are widespread in
cancers. DNA methylation of promoter-associated CpG
islands is an alternate mechanism to mutation in
silencing gene function, and affects tumor-suppressor
genes such as p16 and RBl, growth and differentiation
controlling genes such as ER and many others. Evidence
is now accumulating that some of these methylation
changes may initiate in subpopulations of normal cells as
a function of age and progressively increase during
carcinogenesis. Age-related methylation appears to be
widespread and is one of the earliest changes marking
the risk for neoplasia. In colon cancer, we have shown a
pattern of age-related methylation for several genes,
including ER, IGF2, N33 and MyoD, which progresses
to full methylation in adenomas and neoplasms .
Hypermethylation of these genes is associated with gene
silencing. Age-related methylation involves at least 50%
of the genes which are hypermethylated in colon cancer,
and we propose that such age-related methylation may
partly account for the fact that most cancers occur as a
function of old age. Age-related methylation, then, may
be a fundamental mark of the field defect in patients
with neoplasia. The causes of age-related methylation
are still unknown at this point, but evidence points to an
interplay between local predisposing factors in DNA
(methylation centers), levels of gene expression and
environmental exposure. The concept that age-related
methylation is a predisposing factor for neoplasia
implies that it may serve as a diagnostic risk marker in
cancer, and as a novel target for chemoprevention.
Studies in animal models support this hypothesis and
should lead to novel approaches to risk-assessment and
chemoprevention in humans.
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Citation
Histology and Histopathology, Vol. 15, n.º 3 (2000)
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