Influence of folate status on genomic DNA methylation in colonic mucosa of subjects without colorectal adenoma or cancer.

Maria M Pufulete, R Al-Ghnaniem, J A Rennie, P Appleby, N Harris, S Gout, PW Emery, TA Sanders

Research output: Contribution to journalArticle (Academic Journal)

67 Citations (Scopus)

Abstract

DNA hypomethylation may increase the risk of colorectal cancer. The main aim of this study was to assess the influence of folate status (serum and erythrocyte folate and plasma homocysteine concentrations) on DNA methylation. Methylenetetrahydrofolate reductase (MTHFR 677C --> T and 1298A --> C), methionine synthase (MS 2756A --> G) and cystathionine synthase (CBS 844ins68) polymorphisms were measured to account for potential confounding effects on folate status and DNA methylation. A total of 68 subjects (33 men and 35 women, 36-78 years) free from colorectal polyps or cancer were recruited in a cross-sectional study. Tissue biopsies were obtained at colonoscopy for the determination of DNA methylation in colonic mucosa using an in vitro radiolabelled methyl acceptance assay. Serum and erythrocyte folate were inversely correlated with plasma homocysteine (r=-0.573, P<0.001 and r=-0.307, P=0.01 respectively) and DNA hypomethylation in colonic mucosa (r=-0.311, P=0.01 and r=-0.356, P=0.03). After adjusting for gender, age, body mass index, smoking and genotype, there were weak negative associations between serum and erythrocyte folate and colonic DNA hypomethylation (P=0.07 and P=0.08, respectively).
Original languageEnglish
Pages (from-to)838-842
Number of pages5
JournalBritish Journal of Cancer
Volume92
Issue number5
DOIs
Publication statusPublished - 14 Mar 2005

Keywords

  • 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase
  • Alcohol Drinking
  • Colon
  • Colonoscopy
  • Cystathionine beta-Synthase
  • DNA
  • DNA Methylation
  • Erythrocytes
  • Female
  • Folic Acid
  • Homocysteine
  • Humans
  • Intestinal Mucosa
  • Male
  • Methylenetetrahydrofolate Reductase (NADPH2)
  • Middle Aged
  • Polymorphism, Single Nucleotide
  • Reference Values

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