Skip Navigation

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (91)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Snyderwine, E. G.
Right arrow Articles by Schut, H. A.J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Snyderwine, E. G.
Right arrow Articles by Schut, H. A.J.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© 1993 Oxford University Press

research-article

32P-Postlabeling analysis of IQ, MelQx and PhIP adducts formed in vitro in DNA and polynucleotides and found in vivo in hepatic DNA from IQ-, MelQx- and PhIP-treated monkeys

Elizabeth G. Snyderwine, Cindy D. Davis, Kazuhiro Nouso, Peter P. Roller 1 and Herman A.J. Schut 2

Laboratory of Experimental Carcinogenesis, National Cancer Institute Bethesda, MD
1Laboratory of Medicinal Chemistry, National Cancer Institute Bethesda, MD
2Department of Pathology, Medical College of Ohio Toledo, OH, USA

The 32P-postlabeling method was used to examine the adducts in DNA, polynucleotides, and mononucleotides reacted in vitro with the N-hydroxy and N-acetoxy derivatives of 2-amino-3-methylimidazo[4,5-f]quinoline (IQ), 2-amino-3, 8-dimethylimidazo[4,5-f]quinoxaline (MelQx) or 2-amino-1-methy1-6-phenylimidazo[4,5-b]pyridine (PhIP). Adduct profiles were compared to those found in vivo in liver of cynomolgus monkeys fed IQ, MeIQx or PhIP. The N-acetoxy derivatives of IQ, MelQx and PhIP (generated in situ from the corresponding N-hydroxylamine in the presence of acetic anhydride) each formed three principal adducts in DNA. Adduct 1 of IQ, MeIQx and PhlP was chromatographically identical to the 32P-labeled bis(phosphate) derivative of N-(deoxyguanosin-8-yI)-IQ, N-(deoxyguanosin-8-yI)-MeIQx, and N-(deoxyguanosin-8-yl)-PhIP respectively, and this adduct comprised ~65% of total adduct levels found in DNA in vitro. The C8-guanine adduct and the two minor adducts were also found in poly(dG-dC).poly(dG-dC), suggesting that the two minor adducts of IQ, MelQx and PhIP are also formed on the guanine base. The N-acetoxy derivatives of IQ, MeIQx, and to a much lesser extent PhIP, also formed adducts with adenine-containing polynucleotides including poly(dA), poly(dA).poly(dT) and poly(dA-dT).poly(dA-dT), but these adenine adducts were chromatographically different from those found in DNA. The three guanine adducts of N-acetoxy-IQ, -MeIQx and -PhIP found in vitro in DNA and in guanine-containing polynucleotides were also found in the liver of monkeys fed IQ, MeIQx or PhIP respectively, indicating that metabolic activation via N-hydroxylation and esterification occurred in vivo in monkeys. With each compound, the C8-guanine adduct was the predominant adduct found in vivo. The results indicate similarities among IQ, MeIQx and PhIP in the DNA adducts formed in vitro and in vivo and substantiate the use of the 32P-postlabeling method for comparative adduct studies.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
J. Biol. Chem.Home page
H. Fukuda, T. Takamura-Enya, Y. Masuda, T. Nohmi, C. Seki, K. Kamiya, T. Sugimura, C. Masutani, F. Hanaoka, and H. Nakagama
Translesional DNA Synthesis through a C8-Guanyl Adduct of 2-Amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) in Vitro: REV1 INSERTS dC OPPOSITE THE LESION, AND DNA POLYMERASE {kappa} POTENTIALLY CATALYZES EXTENSION REACTION FROM THE 3'-dC TERMINUS
J. Biol. Chem., September 18, 2009; 284(38): 25585 - 25592.
[Abstract] [Full Text] [PDF]


Home page
Toxicol SciHome page
A. Nishikawa, T. Imazawa, Y. Kuroiwa, Y. Kitamura, K. Kanki, Y. Ishii, T. Umemura, and M. Hirose
Induction of Colon Tumors in C57BL/6J Mice Fed MeIQx, IQ, or PhIP Followed by Dextran Sulfate Sodium Treatment
Toxicol. Sci., April 1, 2005; 84(2): 243 - 248.
[Abstract] [Full Text] [PDF]


Home page
Cancer Epidemiol. Biomarkers Prev.Home page
J. Zhu, P. Chang, M. L. Bondy, A. A. Sahin, S. E. Singletary, S. Takahashi, T. Shirai, and D. Li
Detection of 2-Amino-1-Methyl-6-Phenylimidazo[4,5-b]-Pyridine-DNA Adducts in Normal Breast Tissues and Risk of Breast Cancer
Cancer Epidemiol. Biomarkers Prev., September 1, 2003; 12(9): 830 - 837.
[Abstract] [Full Text] [PDF]


Home page
Cancer Res.Home page
I.-L. Steffensen, H. A. J. Schut, J. E. Paulsen, A. Andreassen, and J. Alexander
Intestinal Tumorigenesis in Multiple Intestinal Neoplasia Mice Induced by the Food Mutagen 2-Amino-1-methyl-6-phenylimidazo[4,5-b]pyridine: Perinatal Susceptibility, Regional Variation, and Correlation with DNA Adducts
Cancer Res., December 1, 2001; 61(24): 8689 - 8696.
[Abstract] [Full Text] [PDF]


Home page
CarcinogenesisHome page
S. Murray, B. G. Lake, S. Gray, A. J. Edwards, C. Springall, E. A. Bowey, G. Williamson, A. R. Boobis, and N. J. Gooderham
Effect of cruciferous vegetable consumption on heterocyclic aromatic amine metabolism in man
Carcinogenesis, September 1, 2001; 22(9): 1413 - 1420.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
K. Brown, E. A. Guenther, K. H. Dingley, M. Cosman, C. A. Harvey, S. J. Shields, and K. W. Turteltaub
Synthesis and spectroscopic characterization of site-specific 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine oligodeoxyribonucleotide adducts
Nucleic Acids Res., May 1, 2001; 29(9): 1951 - 1959.
[Abstract] [Full Text] [PDF]


Home page
CarcinogenesisHome page
G. Paladino, B. Weibel, and C. Sengstag
Heterocyclic aromatic amines efficiently induce mitotic recombination in metabolically competent Saccharomyces cerevisiae strains
Carcinogenesis, November 1, 1999; 20(11): 2143 - 2152.
[Abstract] [Full Text] [PDF]


Home page
CarcinogenesisHome page
C. Y. Wang, M. Debiec-Rychter, H. A.J. Schut, P. Morse, R. F. Jones, C. Archer, C. M. King, and G. P. Haas
N-Acetyltransferase expression and DNA binding of N-hydroxyheterocyclic amines in human prostate epithelium
Carcinogenesis, August 1, 1999; 20(8): 1591 - 1596.
[Abstract] [Full Text] [PDF]


Home page
Cancer Res.Home page
D.-Y. Ryu, V. S. W. Pratt, C. D. Davis, H. A. J. Schut, and E. G. Snyderwine
In Vivo Mutagenicity and Hepatocarcinogenicity of 2-Amino-3,8-dimethylimidazo[4,5-f]quinoxaline (MeIQx) in Bitransgenic c-myc/{{lambda}}lacZ Mice
Cancer Res., June 1, 1999; 59(11): 2587 - 2592.
[Abstract] [Full Text] [PDF]


Home page
CarcinogenesisHome page
H. A.J. Schut and E. G. Snyderwine
DNA adducts of heterocyclic amine food mutagens: implications for mutagenesis and carcinogenesis
Carcinogenesis, March 1, 1999; 20(3): 353 - 368.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
M. S. Solomon, P.-M. L. Morgenthaler, R. J. Turesky, and J. M. Essigmann
Mutational and DNA Binding Specificity of the Carcinogen 2-Amino-3,8-dimethylimidazo[4,5-f]quinoxaline
J. Biol. Chem., August 2, 1996; 271(31): 18368 - 18374.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.