Pregled bibliografske jedinice broj: 372455
N2-Ethyldeoxyguanosine as a potential biomarker for assessing effects of alcohol consumption on DNA
N2-Ethyldeoxyguanosine as a potential biomarker for assessing effects of alcohol consumption on DNA // Cancer Epidemiology Biomarkers and Prevention, 17 (2008), 11; 3026-3032 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 372455 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
N2-Ethyldeoxyguanosine as a potential biomarker for assessing effects of alcohol consumption on DNA
Autori
Balbo, Silvia ; Hashibe, Mia ; Gundy, Sarolta ; Brennan, Paul ; Canova, Cristina ; Simonato, Lorenzo ; Merletti, Franco ; Richiardi, Lorenzo ; Agudo, Antonio ; Castellsague, Xavier ; Znaor, Ariana ; Talamini, Renato ; Bencko, Vladimir ; Holcatova, Ivana ; Wang, Myngiayo ; Hecht, Stephen S. ; Boffetta, Paolo
Izvornik
Cancer Epidemiology Biomarkers and Prevention (1055-9965) 17
(2008), 11;
3026-3032
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
head and neck cancer; alcohol consumption; biomarkers
Sažetak
Head and neck cancers are causally related to alcohol consumption, but the underlying mechanisms are unclear. Ethanol is metabolized to acetaldehyde, an experimental carcinogen. Quantitation of the major DNA adduct of acetaldehyde, N2-ethylidenedeoxyguanosine, in human tissues could help to elucidate the mechanism of alcohol carcinogenicity. We applied a quantitative method for the analysis of this adduct, measured as the NaBH3CN reduction product N2-ethyldeoxyguanosine (N2-ethyl-dGuo) by liquid chromatography-electrospray ionization-tandem mass spectrometry-selected reaction monitoring, on DNA (0.04 +/- 0.03 mg) isolated from blood collected from control subjects recruited from two studies conducted in different areas of Europe between 1999 and 2005. The group selected from the first study (n = 127) included alcohol drinkers and abstainers while the group from the second study (n = 50) included only heavy drinkers. N2-ethyl-dGuo was detected in all DNA samples. After adjusting for potential confounders, in the first study, drinkers showed a higher level of N2-ethyl-dGuo (5, 270 +/- 8, 770 fmol/micromol dGuo) compared with nondrinkers (2, 690 +/- 3040 fmol/micromol dGuo ; P = 0.04). A significant trend according to dose was observed in both studies (P = 0.02 and 0.04, respectively). Taking into account the amount of alcohol consumption, adduct levels were higher in younger compared with older subjects (P = 0.01), whereas no differences were observed comparing men with women. These results show the feasibility of quantifying N2-ethyl-dGuo in small-volume blood samples and are consistent with the hypothesis that ethanol contributes to carcinogenesis through DNA adducts formation.
Izvorni jezik
Engleski
Znanstvena područja
Javno zdravstvo i zdravstvena zaštita
POVEZANOST RADA
Projekti:
005-1080315-0294 - Odrednice multiplih primarnih sijela raka u populaciji (Znaor, Ariana, MZOS ) ( CroRIS)
Ustanove:
Hrvatski zavod za javno zdravstvo,
Medicinski fakultet, Zagreb
Profili:
Ariana Znaor
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE