Increased levels of the acetaldehyde-derived DNA adduct N2-ethyldeoxyguanosine in oral mucosa DNA from Rhesus monkeys exposed to alcohol

Silvia Balbo, Rita Cervera Juanes, Samir Khariwala, Erich J. Baker, James B. Daunais, Kathleen A. Grant

Research output: Contribution to journalArticlepeer-review

23 Scopus citations

Abstract

Alcohol is a human carcinogen. A causal link has been established between alcohol drinking and cancers of the upper aerodigestive tract, colon, liver and breast. Despite this established association, the underlying mechanisms of alcohol-induced carcinogenesis remain unclear. Various mechanisms may come into play depending on the type of cancer; however, convincing evidence supports the concept that ethanol's major metabolite acetaldehyde may play a major role. Acetaldehyde can react with DNA forming adducts which can serve as biomarkers of carcinogen exposure and potentially of cancer risk. The major DNA adduct formed from this reaction is N 2-ethylidenedeoxyguanosine, which can be quantified as its reduced form N 2-ethyl-dG by LC-ESI-MS/MS. To investigate the potential use of N 2-ethyl-dG as a biomarker of alcohol-induced DNA damage, we quantified this adduct in DNA from the oral, oesophageal and mammary gland tissues from rhesus monkeys exposed to alcohol drinking over their lifetimes and compared it to controls. N 2-Ethyl-dG levels were significantly higher in the oral mucosa DNA of the exposed animals. Levels of the DNA adduct measured in the oesophageal mucosa of exposed animals were not significantly different from controls. A correlation between the levels measured in the oral and oesophageal DNA, however, was observed, suggesting a common source of formation of the DNA adducts. N 2 -Ethyl-dG was measured in mammary gland DNA from a small cohort of female animals, but no difference was observed between exposed animals and controls. These results support the hypothesis that acetaldehyde induces DNA damage in the oral mucosa of alcohol-exposed animals and that it may play role in the alcohol-induced carcinogenic process. The decrease of N 2-ethyl-dG levels in exposed tissues further removed from the mouth also suggests a role of alcohol metabolism in the oral cavity, which may be considered separately from ethanol liver metabolism in the investigation of ethanol-related cancer risk.

Original languageEnglish (US)
Pages (from-to)553-558
Number of pages6
JournalMutagenesis
Volume31
Issue number5
DOIs
StatePublished - Sep 1 2016

Bibliographical note

Funding Information:
National Institute of Environmental Health Sciences (ES-11297); National Institute on Alcohol Abuse and Alcoholism (AA019431). Mass spectrometry was carried out in the Analytical Biochemistry core facility of the Masonic Cancer Center, supported in part by Cancer Center Support Grant CA-77598.

Publisher Copyright:
© The Author 2016. Published by Oxford University Press on behalf of the UK Environmental Mutagen Society.

Fingerprint

Dive into the research topics of 'Increased levels of the acetaldehyde-derived DNA adduct N2-ethyldeoxyguanosine in oral mucosa DNA from Rhesus monkeys exposed to alcohol'. Together they form a unique fingerprint.

Cite this