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176 related items for PubMed ID: 17224140

  • 1. Formation of depurinating N3adenine and N7guanine adducts after reaction of 1,2-naphthoquinone or enzyme-activated 1,2-dihydroxynaphthalene with DNA. Implications for the mechanism of tumor initiation by naphthalene.
    Saeed M, Higginbotham S, Rogan E, Cavalieri E.
    Chem Biol Interact; 2007 Feb 20; 165(3):175-88. PubMed ID: 17224140
    [Abstract] [Full Text] [Related]

  • 2. Depurinating naphthalene-DNA adducts in mouse skin related to cancer initiation.
    Saeed M, Higginbotham S, Gaikwad N, Chakravarti D, Rogan E, Cavalieri E.
    Free Radic Biol Med; 2009 Oct 01; 47(7):1075-81. PubMed ID: 19619639
    [Abstract] [Full Text] [Related]

  • 3. Formation of the depurinating N3adenine and N7guanine adducts by reaction of DNA with hexestrol-3',4'-quinone or enzyme-activated 3'-hydroxyhexestrol. Implications for a unifying mechanism of tumor initiation by natural and synthetic estrogens.
    Saeed M, Gunselman SJ, Higginbotham S, Rogan E, Cavalieri E.
    Steroids; 2005 Jan 01; 70(1):37-45. PubMed ID: 15610895
    [Abstract] [Full Text] [Related]

  • 4. Formation of depurinating N3Adenine and N7Guanine adducts by MCF-10F cells cultured in the presence of 4-hydroxyestradiol.
    Saeed M, Rogan E, Fernandez SV, Sheriff F, Russo J, Cavalieri E.
    Int J Cancer; 2007 Apr 15; 120(8):1821-4. PubMed ID: 17230531
    [Abstract] [Full Text] [Related]

  • 5. The greater reactivity of estradiol-3,4-quinone vs estradiol-2,3-quinone with DNA in the formation of depurinating adducts: implications for tumor-initiating activity.
    Zahid M, Kohli E, Saeed M, Rogan E, Cavalieri E.
    Chem Res Toxicol; 2006 Jan 15; 19(1):164-72. PubMed ID: 16411670
    [Abstract] [Full Text] [Related]

  • 6. Catechol quinones of estrogens in the initiation of breast, prostate, and other human cancers: keynote lecture.
    Cavalieri E, Rogan E.
    Ann N Y Acad Sci; 2006 Nov 15; 1089():286-301. PubMed ID: 17261777
    [Abstract] [Full Text] [Related]

  • 7. Expanded analysis of benzo[a]pyrene-DNA adducts formed in vitro and in mouse skin: their significance in tumor initiation.
    Chen L, Devanesan PD, Higginbotham S, Ariese F, Jankowiak R, Small GJ, Rogan EG, Cavalieri EL.
    Chem Res Toxicol; 1996 Nov 15; 9(5):897-903. PubMed ID: 8828927
    [Abstract] [Full Text] [Related]

  • 8. Metabolism and DNA binding studies of 4-hydroxyestradiol and estradiol-3,4-quinone in vitro and in female ACI rat mammary gland in vivo.
    Li KM, Todorovic R, Devanesan P, Higginbotham S, Köfeler H, Ramanathan R, Gross ML, Rogan EG, Cavalieri EL.
    Carcinogenesis; 2004 Feb 15; 25(2):289-97. PubMed ID: 14578156
    [Abstract] [Full Text] [Related]

  • 9. The molecular etiology and prevention of estrogen-initiated cancers: Ockham's Razor: Pluralitas non est ponenda sine necessitate. Plurality should not be posited without necessity.
    Cavalieri E, Rogan E.
    Mol Aspects Med; 2014 Apr 15; 36():1-55. PubMed ID: 23994691
    [Abstract] [Full Text] [Related]

  • 10. A unifying mechanism in the initiation of cancer and other diseases by catechol quinones.
    Cavalieri EL, Rogan EG.
    Ann N Y Acad Sci; 2004 Dec 15; 1028():247-57. PubMed ID: 15650250
    [Abstract] [Full Text] [Related]

  • 11. Synthesis of depurinating DNA adducts formed by one-electron oxidation of 7H-dibenzo[c,g]carbazole and identification of these adducts after activation with rat liver microsomes.
    Chen L, Devanesan PD, Byun J, Gooden JK, Gross ML, Rogan EG, Cavalieri EL.
    Chem Res Toxicol; 1997 Feb 15; 10(2):225-33. PubMed ID: 9049435
    [Abstract] [Full Text] [Related]

  • 12. Synthesis and structure determination of 6-methylbenzo[a]pyrene-deoxyribonucleoside adducts and their identification and quantitation in vitro and in mouse skin.
    Hanson AA, Li KM, Lin CH, Jankowiak R, Small GJ, Rogan EG, Cavalieri EL.
    Chem Biol Interact; 2000 Aug 15; 128(1):65-90. PubMed ID: 10996301
    [Abstract] [Full Text] [Related]

  • 13. Benzene and dopamine catechol quinones could initiate cancer or neurogenic disease.
    Zahid M, Saeed M, Rogan EG, Cavalieri EL.
    Free Radic Biol Med; 2010 Jan 15; 48(2):318-24. PubMed ID: 19909805
    [Abstract] [Full Text] [Related]

  • 14. Mechanism of metabolic activation and DNA adduct formation by the human carcinogen diethylstilbestrol: the defining link to natural estrogens.
    Saeed M, Rogan E, Cavalieri E.
    Int J Cancer; 2009 Mar 15; 124(6):1276-84. PubMed ID: 19089919
    [Abstract] [Full Text] [Related]

  • 15. Catechol ortho-quinones: the electrophilic compounds that form depurinating DNA adducts and could initiate cancer and other diseases.
    Cavalieri EL, Li KM, Balu N, Saeed M, Devanesan P, Higginbotham S, Zhao J, Gross ML, Rogan EG.
    Carcinogenesis; 2002 Jun 15; 23(6):1071-7. PubMed ID: 12082031
    [Abstract] [Full Text] [Related]

  • 16. Inhibition of depurinating estrogen-DNA adduct formation by natural compounds.
    Zahid M, Gaikwad NW, Rogan EG, Cavalieri EL.
    Chem Res Toxicol; 2007 Dec 15; 20(12):1947-53. PubMed ID: 18039013
    [Abstract] [Full Text] [Related]

  • 17. Identification and quantitation of dibenzo[a,l]pyrene--DNA adducts formed by rat liver microsomes in vitro: preponderance of depurinating adducts.
    Li KM, Todorovic R, Rogan EG, Cavalieri EL, Ariese F, Suh M, Jankowiak R, Small GJ.
    Biochemistry; 1995 Jun 27; 34(25):8043-9. PubMed ID: 7794917
    [Abstract] [Full Text] [Related]

  • 18. Synthesis and structure determination of the adducts formed by electrochemical oxidation of 1,2,3,4-Tetrahydro-7,12-dimethylbenz[a]anthracene in the presence of deoxyribonucleosides or adenine.
    Mulder PP, Chen L, Sekhar BC, George M, Gross ML, Rogan EG, Cavalieri EL.
    Chem Res Toxicol; 1996 Dec 27; 9(8):1264-77. PubMed ID: 8951228
    [Abstract] [Full Text] [Related]

  • 19. Metabolic activation and formation of DNA adducts of hexestrol, a synthetic nonsteroidal carcinogenic estrogen.
    Jan ST, Devanesan PD, Stack DE, Ramanathan R, Byun J, Gross ML, Rogan EG, Cavalieri EL.
    Chem Res Toxicol; 1998 May 27; 11(5):412-9. PubMed ID: 9585471
    [Abstract] [Full Text] [Related]

  • 20. Investigation by mass spectrometry and 32P post-labelling of DNA adducts formation from 1,2-naphthoquinone, an oxydated metabolite of naphthalene.
    Clergé A, Le Goff J, Lopez-Piffet C, Meier S, Lagadu S, Vaudorne I, Babin V, Cailly T, Delépée R.
    Chemosphere; 2021 Jan 27; 263():128079. PubMed ID: 33297078
    [Abstract] [Full Text] [Related]

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