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Publication Detail

Title: LINE-1 methylation in leukocyte DNA, interaction with phosphatidylethanolamine N-methyltransferase variants and bladder cancer risk.

Authors: Tajuddin, S M; Amaral, A F S; Fernández, A F; Chanock, S; Silverman, D T; Tardón, A; Carrato, A; García-Closas, M; Jackson, B P; Toraño, E G; Márquez, M; Urdinguio, R G; García-Closas, R; Rothman, N; Kogevinas, M; Real, F X; Fraga, M F; Malats, N; Spanish Bladder Cancer/EPICURO Study investigators

Published In Br J Cancer, (2014 Apr 15)

Abstract: Aberrant global DNA methylation is shown to increase cancer risk. LINE-1 has been proven a measure of global DNA methylation. The objectives of this study were to assess the association between LINE-1 methylation level and bladder cancer risk and to evaluate effect modification by environmental and genetic factors.Bisulphite-treated leukocyte DNA from 952 cases and 892 hospital controls was used to measure LINE-1 methylation level at four CpG sites by pyrosequencing. Logistic regression model was fitted to estimate odds ratios (ORs) and 95% confidence intervals (95% CIs). Interactions between LINE-1 methylation levels and environmental and genetic factors were assessed.The risk of bladder cancer followed a nonlinear association with LINE-1 methylation. Compared with subjects in the middle tertile, the adjusted OR for subjects in the lower and the higher tertiles were 1.26 (95% CI 0.99-1.60, P=0.06) and 1.33 (95% CI 1.05-1.69, P=0.02), respectively. This association significantly increased among individuals homozygous for the major allele of five single-nucleotide polymorphisms located in the phosphatidylethanolamine N-methyltransferase gene (corrected P-interaction<0.05).The findings from this large-scale study suggest that both low and high levels of global DNA methylation are associated with the risk of bladder cancer.

PubMed ID: 24595004 Exiting the NIEHS site

MeSH Terms: Aged; Aged, 80 and over; CpG Islands/genetics; DNA Methylation/genetics*; Female; Genetic Association Studies; Genetic Predisposition to Disease; High-Throughput Nucleotide Sequencing; Humans; Leukocytes/pathology; Long Interspersed Nucleotide Elements/genetics*; Male; Middle Aged; Phosphatidylethanolamine N-Methyltransferase/genetics*; Polymorphism, Single Nucleotide; Risk Factors; Urinary Bladder Neoplasms/genetics*; Urinary Bladder Neoplasms/pathology

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