Back to Search Start Over

Sex-specific association of sequence variants in CBS and MTRR with risk for promoter hypermethylation in the lung epithelium of smokers

Authors :
Christine A. Stidley
Jill M. Siegfried
Marianne Berwick
Sally P. Stabler
Shuguang Leng
Tim Byers
Maria A. Picchi
Steven A. Belinsky
Amanda J. Mackey
Kristina G. Flores
Publication Year :
2012
Publisher :
Oxford University Press, 2012.

Abstract

Gene promoter hypermethylation is now regarded as a promising biomarker for the risk and progression of lung cancer. The one-carbon metabolism pathway is postulated to affect deoxyribonucleic acid (DNA) methylation because it is responsible for the generation of S-adenosylmethionine (SAM), the methyl donor for cellular methylation reactions. This study investigated the association of single nucleotide polymorphisms (SNPs) in six one-carbon metabolism-related genes with promoter hypermethylation in sputum DNA from non-Hispanic white smokers in the Lovelace Smokers Cohort (LSC) (n = 907). Logistic regression was used to assess the association of SNPs with hypermethylation using a high/low methylation cutoff. SNPs in the cystathionine beta synthase (CBS) and 5-methyltetrahydrofolate-homocysteine methyltransferase reductase (MTRR) genes were significantly associated with high methylation in males [CBS rs2850146 (-8283G > C), OR = 4.9; 95% CI: 1.98, 12.2, P = 0.0006] and low methylation in females [MTRR rs3776467 (7068A > G), OR = 0.57, 95% CI: 0.42, 0.77, P = 0.0003]. The variant allele of rs2850146 was associated with reduced gene expression and increased plasma homocysteine (Hcy) concentrations. Three plasma metabolites, Hcy, methionine and dimethylglycine, were associated with increased risk for gene methylation. These studies suggest that SNPs in CBS and MTRR have sex-specific associations with aberrant methylation in the lung epithelium of smokers that could be mediated by the affected one-carbon metabolism and transsulfuration in the cells. Abbreviations: CBS cystathionine beta synthase DNA deoxyribonucleic acid HBEC human bronchial epithelial cell Hcy homocysteine LD, linkage disequilibrium; LSC lovelace Smokers Cohort MAF minor allele frequency MTHFR methylenetetrahydrofolate reductase MTRR methyltransferase reductase SNP single nucleotide polymorphisms SAH S-adenosylhomocysteine SAM S-adenosylmethionine

Details

Language :
English
Database :
OpenAIRE
Accession number :
edsair.doi.dedup.....2ab5c7109a0d56291c8ba8e01f55ecb2