Vitamin C prevents DNA mutation induced by oxidative stress Journal Article


Authors: Lutsenko, E. A.; Cárcamo, J. M.; Golde, D. W.
Article Title: Vitamin C prevents DNA mutation induced by oxidative stress
Abstract: The precise role of vitamin C in the prevention of DNA mutations is controversial. Although ascorbic acid has strong antioxidant properties, it also has pro-oxidant effects in the presence of free transition metals. Vitamin C was recently reported to induce the decomposition of lipid hydroperoxides independent of metal interactions, suggesting that it may cause DNA damage. To directly address the role of vitamin C in maintaining genomic integrity we developed a genetic system for quantifying guanine base mutations induced in human cells under oxidative stress. The assay utilized a plasmid construct encoding the cDNA for chloramphenicol acetyl transferase modified to contain an amber stop codon, which was restored to wild type by G to T transversion induced by oxidative stress. The mutation frequency was determined from the number of plasmids containing the wild type chloramphenicol acetyl transferase gene rescued from oxidatively stressed cells. Cells were loaded with vitamin C by exposing them to dehydroascorbic acid, thereby avoiding transition metal-related pro-oxidant effects of ascorbic acid. We found that vitamin C loading resulted in substantially decreased mutations induced by H2O2. Depletion of glutathione led to cytotoxicity and an increase in H2O2-induced mutation frequency; however, mutation frequency was prominently decreased in depleted cells preloaded with vitamin C. The mutation results correlated with a decrease in total 8-oxo-guanine measured in genomic DNA of cells loaded with vitamin C and oxidatively stressed. These findings directly support the concept that high intracellular concentrations of vitamin C can prevent oxidation-induced mutations in human cells.
Keywords: controlled study; gene mutation; human cell; mutation; quantitative assay; dna damage; genes; models, biological; oxygen; cell line; alleles; cytotoxicity; dose-response relationship, drug; tyrosine; wild type; correlation analysis; dna; drug mechanism; guanine; plasmid; cellular distribution; plasmids; lipids; hydrogen peroxide; oxidative stress; antioxidants; ascorbic acid; antioxidant activity; mutation rate; lipid peroxidation; mutagenesis; dehydroascorbic acid; glutathione; complementary dna; dna, complementary; gene construct; 8 hydroxyguanine; cells; vitamins; hl-60 cells; oxidizing agent; metal binding; vitamin metabolism; decomposition; humans; human; priority journal; article; chloramphenicol acetyltransferase; chloramphenicol o-acetyltransferase; transition metals; glutathione metabolism
Journal Title: Journal of Biological Chemistry
Volume: 277
Issue: 19
ISSN: 0021-9258
Publisher: American Society for Biochemistry and Molecular Biology  
Date Published: 2002-05-10
Start Page: 16895
End Page: 16899
Language: English
DOI: 10.1074/jbc.M201151200
PUBMED: 11884413
PROVIDER: scopus
DOI/URL:
Notes: Export Date: 14 November 2014 -- Source: Scopus
Altmetric
Citation Impact
BMJ Impact Analytics
MSK Authors
  1. David Golde
    127 Golde
  2. Juan O Carcamo
    31 Carcamo