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Journal Abstract Search

254 related items for PubMed ID: 16696575

  • 1. Polycyclic aromatic hydrocarbon (PAH) o-quinones produced by the aldo-keto-reductases (AKRs) generate abasic sites, oxidized pyrimidines, and 8-oxo-dGuo via reactive oxygen species.
    Park JH, Troxel AB, Harvey RG, Penning TM.
    Chem Res Toxicol; 2006 May; 19(5):719-28. PubMed ID: 16696575
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  • 6. The pattern of p53 mutations caused by PAH o-quinones is driven by 8-oxo-dGuo formation while the spectrum of mutations is determined by biological selection for dominance.
    Park JH, Gelhaus S, Vedantam S, Oliva AL, Batra A, Blair IA, Troxel AB, Field J, Penning TM.
    Chem Res Toxicol; 2008 May; 21(5):1039-49. PubMed ID: 18489080
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  • 7. Reactive oxygen species generated by PAH o-quinones cause change-in-function mutations in p53.
    Yu D, Berlin JA, Penning TM, Field J.
    Chem Res Toxicol; 2002 Jun; 15(6):832-42. PubMed ID: 12067251
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  • 8. Redox cycling of catechol estrogens generating apurinic/apyrimidinic sites and 8-oxo-deoxyguanosine via reactive oxygen species differentiates equine and human estrogens.
    Wang Z, Chandrasena ER, Yuan Y, Peng KW, van Breemen RB, Thatcher GR, Bolton JL.
    Chem Res Toxicol; 2010 Aug 16; 23(8):1365-73. PubMed ID: 20509668
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  • 9. DNA strand scission by polycyclic aromatic hydrocarbon o-quinones: role of reactive oxygen species, Cu(II)/Cu(I) redox cycling, and o-semiquinone anion radicals,
    Flowers L, Ohnishi ST, Penning TM.
    Biochemistry; 1997 Jul 15; 36(28):8640-8. PubMed ID: 9214311
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  • 11. Aldo-keto reductases protect lung adenocarcinoma cells from the acute toxicity of B[a]P-7,8-trans-dihydrodiol.
    Abedin Z, Sen S, Field J.
    Chem Res Toxicol; 2012 Jan 13; 25(1):113-21. PubMed ID: 22053912
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  • 12. Redox cycling of polycyclic aromatic hydrocarbon o-quinones: metal ion-catalyzed oxidation of catechols bypasses inhibition by superoxide dismutase.
    Jarabak R, Harvey RG, Jarabak J.
    Chem Biol Interact; 1998 Oct 02; 115(3):201-13. PubMed ID: 9851290
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  • 13. Activation of polycyclic aromatic hydrocarbon trans-dihydrodiol proximate carcinogens by human aldo-keto reductase (AKR1C) enzymes and their functional overexpression in human lung carcinoma (A549) cells.
    Palackal NT, Lee SH, Harvey RG, Blair IA, Penning TM.
    J Biol Chem; 2002 Jul 05; 277(27):24799-808. PubMed ID: 11978787
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  • 15. Oxidative DNA damage induced by benz[a]anthracene metabolites via redox cycles of quinone and unique non-quinone.
    Seike K, Murata M, Oikawa S, Hiraku Y, Hirakawa K, Kawanishi S.
    Chem Res Toxicol; 2003 Nov 05; 16(11):1470-6. PubMed ID: 14615974
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  • 16. Isoform-specific induction of a human aldo-keto reductase by polycyclic aromatic hydrocarbons (PAHs), electrophiles, and oxidative stress: implications for the alternative pathway of PAH activation catalyzed by human dihydrodiol dehydrogenase.
    Burczynski ME, Lin HK, Penning TM.
    Cancer Res; 1999 Feb 01; 59(3):607-14. PubMed ID: 9973208
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  • 17. Dihydrodiol dehydrogenase and its role in polycyclic aromatic hydrocarbon metabolism.
    Penning TM.
    Chem Biol Interact; 1993 Oct 01; 89(1):1-34. PubMed ID: 8221964
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  • 18. Polycyclic aromatic hydrocarbon quinone-mediated oxidation reduction cycling catalyzed by a human placental NADPH-linked carbonyl reductase.
    Jarabak J.
    Arch Biochem Biophys; 1991 Dec 01; 291(2):334-8. PubMed ID: 1659323
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  • 19. The Role of Human Aldo-Keto Reductases in the Metabolic Activation and Detoxication of Polycyclic Aromatic Hydrocarbons: Interconversion of PAH Catechols and PAH o-Quinones.
    Zhang L, Jin Y, Huang M, Penning TM.
    Front Pharmacol; 2012 Dec 01; 3():193. PubMed ID: 23162467
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  • 20. Benzo[a]pyrene-7,8-quinone-3'-mononucleotide adduct standards for 32P postlabeling analyses: detection of benzo[a]pyrene-7,8-quinone-calf thymus DNA adducts.
    Balu N, Padgett WT, Nelson GB, Lambert GR, Ross JA, Nesnow S.
    Anal Biochem; 2006 Aug 15; 355(2):213-23. PubMed ID: 16797471
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