Quantitation of DNA Adducts Resulting from Acrolein Exposure and Lipid Peroxidation in Oral Cells of Cigarette Smokers from Three Racial/Ethnic Groups with Differing Risks for Lung Cancer.

The Multiethnic Cohort Study has demonstrated that the risk for lung cancer in cigarette smokers among three ethnic groups is highest in Native Hawaiians, intermediate in Whites, and lowest in Japanese Americans. We hypothesized that differences in levels of DNA adducts in oral cells of cigarette smokers would be related to these differing risks of lung cancer. Therefore, we used liquid chromatography-nanoelectrospray ionization-high resolution tandem mass spectrometry to quantify the acrolein-DNA adduct (8R/S)-3-(2'-deoxyribos-1'-yl)-5,6,7,8-tetrahydro-8-hydroxypyrimido[1,2-a]purine-10(3H)-one (γ-OH-Acr-dGuo, 1) and the lipid peroxidation-related DNA adduct 1,N6-etheno-dAdo (εdAdo, 2) in DNA obtained by oral rinse from 101 Native Hawaiians, 101 Whites, and 79 Japanese Americans. Levels of urinary biomarkers of nicotine, acrolein, acrylonitrile, and a mixture of crotonaldehyde, methyl vinyl ketone, and methacrolein were also quantified. Whites had significantly higher levels of γ-OH-Acr-dGuo than Japanese Americans and Native Hawaiians after adjusting for age and sex. There was no significant difference in levels of this DNA adduct between Japanese Americans and Native Hawaiians, which is not consistent with the high lung cancer risk of Native Hawaiians. Levels of εdAdo were modestly higher in Whites and Native Hawaiians than in Japanese Americans. The lower level of DNA adducts in the oral cells of Japanese American cigarette smokers than Whites is consistent with their lower risk for lung cancer. The higher levels of εdAdo, but not γ-OH-Acr-dGuo, in Native Hawaiian versus Japanese American cigarette smokers suggest that lipid peroxidation and related processes may be involved in their high risk for lung cancer, but further studies are required.

[1]  D. Hatsukami,et al.  Increased Acrolein-DNA Adducts in Buccal Brushings of e-Cigarette Users. , 2022, Carcinogenesis.

[2]  S. Murphy Biochemistry of nicotine metabolism and its relevance to lung cancer , 2021, The Journal of biological chemistry.

[3]  A. Jemal,et al.  Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries , 2021, CA: a cancer journal for clinicians.

[4]  Roberta Losi Guembarovski,et al.  Effects of GSTT1 and GSTM1 polymorphisms in glutathione levels and breast cancer development in Brazilian patients , 2021, Molecular Biology Reports.

[5]  S. Hecht,et al.  Quantitative Liquid Chromatography-Nanoelectrospray Ionization-High Resolution Tandem Mass Spectrometry Analysis of Acrolein-DNA Adducts and Etheno-DNA Adducts in Oral Cells from Cigarette Smokers and Non-smokers. , 2020, Chemical research in toxicology.

[6]  S. Hecht,et al.  Resolution and quantitation of mercapturic acids derived from crotonaldehyde, methacrolein, and methyl vinyl ketone in the urine of smokers and non-smokers. , 2020, Chemical research in toxicology.

[7]  Tsung-Yun Liu,et al.  Identification of acrolein metabolites in human buccal cells, blood, and urine after consumption of commercial fried food , 2019, Food science & nutrition.

[8]  C. Haiman,et al.  Racial/Ethnic Differences in Lung Cancer Incidence in the Multiethnic Cohort Study: An Update. , 2019, Journal of the National Cancer Institute.

[9]  Xianghua Luo,et al.  Longitudinal stability in cigarette smokers of urinary biomarkers of exposure to the toxicants acrylonitrile and acrolein , 2019, PloS one.

[10]  Christopher A Haiman,et al.  Tobacco biomarkers and genetic/epigenetic analysis to investigate ethnic/racial differences in lung cancer risk among smokers , 2018, npj Precision Oncology.

[11]  W. Rom,et al.  Aldehydes are the predominant forces inducing DNA damage and inhibiting DNA repair in tobacco smoke carcinogenesis , 2018, Proceedings of the National Academy of Sciences.

[12]  M. Graf,et al.  DNA damage by lipid peroxidation products: implications in cancer, inflammation and autoimmunity , 2017, AIMS Genetics.

[13]  S. Hecht,et al.  Oral Cell DNA Adducts as Potential Biomarkers for Lung Cancer Susceptibility in Cigarette Smokers. , 2017, Chemical research in toxicology.

[14]  Yinsheng Wang,et al.  Occurrence, Biological Consequences, and Human Health Relevance of Oxidative Stress-Induced DNA Damage. , 2016, Chemical research in toxicology.

[15]  M. Stratton,et al.  Mutational signatures associated with tobacco smoking in human cancer , 2016, Science.

[16]  B. Blount,et al.  Mainstream Smoke Levels of Volatile Organic Compounds in 50 U.S. Domestic Cigarette Brands Smoked With the ISO and Canadian Intense Protocols. , 2016, Nicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco.

[17]  C. Haiman,et al.  Benzene Uptake and Glutathione S-transferase T1 Status as Determinants of S-Phenylmercapturic Acid in Cigarette Smokers in the Multiethnic Cohort , 2016, PloS one.

[18]  C. Haiman,et al.  Mercapturic Acids Derived from the Toxicants Acrolein and Crotonaldehyde in the Urine of Cigarette Smokers from Five Ethnic Groups with Differing Risks for Lung Cancer , 2015, PloS one.

[19]  L. Le Marchand,et al.  Nicotine N-glucuronidation relative to N-oxidation and C-oxidation and UGT2B10 genotype in five ethnic/racial groups. , 2014, Carcinogenesis.

[20]  M. Oldham,et al.  Insights from analysis for harmful and potentially harmful constituents (HPHCs) in tobacco products. , 2014, Regulatory toxicology and pharmacology : RTP.

[21]  S. Venitt,et al.  DNA and protein adducts in human tissues resulting from exposure to tobacco smoke , 2012, International journal of cancer.

[22]  Stephen S Hecht,et al.  Lung carcinogenesis by tobacco smoke , 2012, International journal of cancer.

[23]  W. Morgan,et al.  Mainstream smoke chemistry analysis of samples from the 2009 US cigarette market. , 2012, Regulatory toxicology and pharmacology : RTP.

[24]  F. Chung,et al.  Regioselective formation of acrolein-derived cyclic 1,N(2)-propanodeoxyguanosine adducts mediated by amino acids, proteins, and cell lysates. , 2012, Chemical research in toxicology.

[25]  H. Haussmann Use of hazard indices for a theoretical evaluation of cigarette smoke composition. , 2012, Chemical research in toxicology.

[26]  H. C. Chen,et al.  Quantitative analysis of multiple exocyclic DNA adducts in human salivary DNA by stable isotope dilution nanoflow liquid chromatography-nanospray ionization tandem mass spectrometry. , 2011, Analytical chemistry.

[27]  W. Atkins,et al.  Interactions of glutathione transferases with 4-hydroxynonenal , 2011, Drug metabolism reviews.

[28]  S. Hecht,et al.  Analysis of acrolein-derived 1,N2-propanodeoxyguanosine adducts in human leukocyte DNA from smokers and nonsmokers. , 2011, Chemical research in toxicology.

[29]  S. Spivack,et al.  Screening for DNA adducts by data-dependent constant neutral loss-triple stage mass spectrometry with a linear quadrupole ion trap mass spectrometer. , 2009, Analytical chemistry.

[30]  A. Cheema,et al.  Detection of the acrolein-derived cyclic DNA adduct by a quantitative 32P-postlabeling/solid-phase extraction/HPLC method: blocking its artifact formation with glutathione. , 2008, Analytical biochemistry.

[31]  J. F. Stevens,et al.  Acrolein: sources, metabolism, and biomolecular interactions relevant to human health and disease. , 2008, Molecular nutrition & food research.

[32]  S. Hecht,et al.  Detection and quantitation of acrolein-derived 1,N2-propanodeoxyguanosine adducts in human lung by liquid chromatography-electrospray ionization-tandem mass spectrometry. , 2007, Chemical research in toxicology.

[33]  S. Hecht,et al.  Tobacco smoke carcinogens and lung cancer. , 1999, Journal of the National Cancer Institute.

[34]  H. C. Chen,et al.  Lipid peroxidation as a potential endogenous source for the formation of exocyclic DNA adducts. , 1996, Carcinogenesis.

[35]  B. Mannervik,et al.  Detoxication of base propenals and other alpha, beta-unsaturated aldehyde products of radical reactions and lipid peroxidation by human glutathione transferases. , 1994, Proceedings of the National Academy of Sciences of the United States of America.