메뉴 건너뛰기




Volumn 18, Issue 4, 2007, Pages 642-650

Liquid Chromatography-Tandem Mass Spectrometry Analysis of the DNA Adducts of Aristolochic Acids

Author keywords

[No Author keywords available]

Indexed keywords

ARISTOLOCHIC ACIDS; DISSOCIATIVE LOSS; DNA ADDUCTS; EXOCYCLIC AMINO GROUP;

EID: 33947304167     PISSN: 10440305     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jasms.2006.11.010     Document Type: Article
Times cited : (37)

References (38)
  • 1
    • 0002050785 scopus 로고    scopus 로고
    • Pressurized Liquid Extraction of Berberine and Aristolochic Acids in Medicinal Plants
    • Ong E.S., Woo S.O., and Yong Y.L. Pressurized Liquid Extraction of Berberine and Aristolochic Acids in Medicinal Plants. J. Chromatogr. A 904 (2000) 57-64
    • (2000) J. Chromatogr. A , vol.904 , pp. 57-64
    • Ong, E.S.1    Woo, S.O.2    Yong, Y.L.3
  • 2
    • 33947476854 scopus 로고
    • Tumor Inhibitors, I. Aristolochic Acid, the Active Principle of Aristolochia indica
    • Kupchan M.S., and Doskotch R.W. Tumor Inhibitors, I. Aristolochic Acid, the Active Principle of Aristolochia indica. J. Med. Pharm. Chem 5 (1962) 657-659
    • (1962) J. Med. Pharm. Chem , vol.5 , pp. 657-659
    • Kupchan, M.S.1    Doskotch, R.W.2
  • 3
    • 0016466633 scopus 로고
    • Aristolochic Acids from Aristolochia manshuriensis
    • Rucker G., and Chung B.S. Aristolochic Acids from Aristolochia manshuriensis. Plant Med 27 (1975) 68-71
    • (1975) Plant Med , vol.27 , pp. 68-71
    • Rucker, G.1    Chung, B.S.2
  • 4
    • 0023866860 scopus 로고
    • DNA Adduct Formation of Aristolochic Acid I and II In Vitro and In Vivo
    • Schmeiser H.H., Schoepe K.B., and Wiessler M. DNA Adduct Formation of Aristolochic Acid I and II In Vitro and In Vivo. Carcinogenesis 9 (1988) 297-303
    • (1988) Carcinogenesis , vol.9 , pp. 297-303
    • Schmeiser, H.H.1    Schoepe, K.B.2    Wiessler, M.3
  • 5
    • 0025181829 scopus 로고
    • Aristolochic Acid Binds Covalently to Exocyclic Amino Group of Purine Nucleotides in DNA
    • Pfau W., Schmeiser H.H., and Wiessler M. Aristolochic Acid Binds Covalently to Exocyclic Amino Group of Purine Nucleotides in DNA. Carcinogenesis 11 (1990) 313-319
    • (1990) Carcinogenesis , vol.11 , pp. 313-319
    • Pfau, W.1    Schmeiser, H.H.2    Wiessler, M.3
  • 6
    • 0025195429 scopus 로고
    • 32P-Postlabelling Analysis of the DNA Adducts Form by Aristolochic Acid I and II
    • 32P-Postlabelling Analysis of the DNA Adducts Form by Aristolochic Acid I and II. Carcinogenesis 11 (1990) 1627-1633
    • (1990) Carcinogenesis , vol.11 , pp. 1627-1633
    • Pfau, W.1    Schmeiser, H.H.2    Wiessler, M.3
  • 7
    • 0025918608 scopus 로고
    • 6-Adenylarylation of DNA by Aristolochic Acid II and a Synthetic Model for the Putative Proximate Carcinogen
    • 6-Adenylarylation of DNA by Aristolochic Acid II and a Synthetic Model for the Putative Proximate Carcinogen. Chem. Res. Toxicol 4 (1991) 581-586
    • (1991) Chem. Res. Toxicol , vol.4 , pp. 581-586
    • Pfau, W.1    Schmeiser, H.H.2    Wiessler, M.3
  • 9
    • 0034861029 scopus 로고    scopus 로고
    • Human Cytochrome P450 Enzymes Involved in the Metabolic Activation of Carcinogenic Aristolochic Acids: Evidence for the Reductive Activation by CYP1A1 and CYP1A2
    • Stiborova M., Frei E., Wiessler M., and Schmeiser H.H. Human Cytochrome P450 Enzymes Involved in the Metabolic Activation of Carcinogenic Aristolochic Acids: Evidence for the Reductive Activation by CYP1A1 and CYP1A2. Chem. Res. Toxicol 14 (2001) 1128-1137
    • (2001) Chem. Res. Toxicol , vol.14 , pp. 1128-1137
    • Stiborova, M.1    Frei, E.2    Wiessler, M.3    Schmeiser, H.H.4
  • 10
    • 0035958272 scopus 로고    scopus 로고
    • Evidence for Reductive Activation of Carcinogenic Aristolochic Acids by Prostaglandin H Synthase-P-32-postlabeling Analysis of DNA Adduct Formation
    • Stiborva M., Frei E., Breuer A., Wiessler M., and Schmeiser H.H. Evidence for Reductive Activation of Carcinogenic Aristolochic Acids by Prostaglandin H Synthase-P-32-postlabeling Analysis of DNA Adduct Formation. Mutat. Res 493 (2001) 149-160
    • (2001) Mutat. Res , vol.493 , pp. 149-160
    • Stiborva, M.1    Frei, E.2    Breuer, A.3    Wiessler, M.4    Schmeiser, H.H.5
  • 11
    • 0142185373 scopus 로고    scopus 로고
    • Human Cytosolic Enzymes Involved in the Metabolic Activation of Carcinogenic Aristolochic Acid: Evidence for Reductive Activation by Human NAD(P)H:Quinone Oxidoreductase
    • Stiborova M., Frei E., Sopko B., Sopkova K., Markova V., Lankova M., Kumstyrova T., Wiessler M., and Schmeiser H.H. Human Cytosolic Enzymes Involved in the Metabolic Activation of Carcinogenic Aristolochic Acid: Evidence for Reductive Activation by Human NAD(P)H:Quinone Oxidoreductase. Carcinogenesis 24 (2003) 1695-1703
    • (2003) Carcinogenesis , vol.24 , pp. 1695-1703
    • Stiborova, M.1    Frei, E.2    Sopko, B.3    Sopkova, K.4    Markova, V.5    Lankova, M.6    Kumstyrova, T.7    Wiessler, M.8    Schmeiser, H.H.9
  • 12
    • 0031408650 scopus 로고    scopus 로고
    • Comparison of DNA Adduct Formation by Aristolochic Acids in Various In Vitro Activation Systems by P-32-post-labelling: Evidence for Reductive Activation by Peroxidases
    • Schmeiser H.H., Frei E., Wiessler M., and Stiborova M. Comparison of DNA Adduct Formation by Aristolochic Acids in Various In Vitro Activation Systems by P-32-post-labelling: Evidence for Reductive Activation by Peroxidases. Carcinogenesis 18 (1997) 1055-1062
    • (1997) Carcinogenesis , vol.18 , pp. 1055-1062
    • Schmeiser, H.H.1    Frei, E.2    Wiessler, M.3    Stiborova, M.4
  • 16
    • 0031284662 scopus 로고    scopus 로고
    • P-32-post-labelling Analysis of DNA Adducts Formed by Aristolochic Acid in Tissues from Patients with Chinese Herbs Nephropathy
    • Bieler C.A., Stiborova M., Wiessler M., Cosyns J.-P., van Ypersele de Strihou C., and Schmeiser H.H. P-32-post-labelling Analysis of DNA Adducts Formed by Aristolochic Acid in Tissues from Patients with Chinese Herbs Nephropathy. Carcinogenesis 18 (1997) 1063-1067
    • (1997) Carcinogenesis , vol.18 , pp. 1063-1067
    • Bieler, C.A.1    Stiborova, M.2    Wiessler, M.3    Cosyns, J.-P.4    van Ypersele de Strihou, C.5    Schmeiser, H.H.6
  • 17
    • 0036257348 scopus 로고    scopus 로고
    • Carcinogenic Aristolochic Acids upon Activation by DT-Diaphorase Form Adducts Found in DNA of Patients with Chinese Herbs Nephropathy
    • Stiborova M., Frei E., Sopko B., Wiessler M., and Schmeiser H.H. Carcinogenic Aristolochic Acids upon Activation by DT-Diaphorase Form Adducts Found in DNA of Patients with Chinese Herbs Nephropathy. Carcinogenesis 23 (2002) 617-625
    • (2002) Carcinogenesis , vol.23 , pp. 617-625
    • Stiborova, M.1    Frei, E.2    Sopko, B.3    Wiessler, M.4    Schmeiser, H.H.5
  • 18
    • 0035948821 scopus 로고    scopus 로고
    • Analyses of DNA Adducts Formed by Ochratoxin A and Aristolochic Acid in Patients with Chinese Herbs Nephropathy
    • Arlt V.M., Pfohl-Loszkowicz A., Cosyns J.-P., and Schmeiser H.H. Analyses of DNA Adducts Formed by Ochratoxin A and Aristolochic Acid in Patients with Chinese Herbs Nephropathy. Mutat. Res 494 (2001) 143-150
    • (2001) Mutat. Res , vol.494 , pp. 143-150
    • Arlt, V.M.1    Pfohl-Loszkowicz, A.2    Cosyns, J.-P.3    Schmeiser, H.H.4
  • 19
    • 0032877481 scopus 로고    scopus 로고
    • Synthesis and Structure Determination of the Adducts Formed by Electrochemical Oxidation of Dibenzo[a,l]pyrene in the Presence of Adenine
    • Li K.M., Byun J., Gross M.L., Zamzow D., Jankowiak R., Rogan E.G., and Cavalieri E.L. Synthesis and Structure Determination of the Adducts Formed by Electrochemical Oxidation of Dibenzo[a,l]pyrene in the Presence of Adenine. Chem. Res. Toxicol 12 (1999) 749-757
    • (1999) Chem. Res. Toxicol , vol.12 , pp. 749-757
    • Li, K.M.1    Byun, J.2    Gross, M.L.3    Zamzow, D.4    Jankowiak, R.5    Rogan, E.G.6    Cavalieri, E.L.7
  • 20
    • 0032984919 scopus 로고    scopus 로고
    • Quantitative Analysis of 4-Aminobiphenyl-C8-deoxyguanosyl DNA Adducts Produced In Vitro and In Vivo Using HPLC-ES-MS
    • Doerge D.R., Chirchwell M.I., Marques M.M., and Beland F.A. Quantitative Analysis of 4-Aminobiphenyl-C8-deoxyguanosyl DNA Adducts Produced In Vitro and In Vivo Using HPLC-ES-MS. Carcinogenesis 20 (1999) 1055-1061
    • (1999) Carcinogenesis , vol.20 , pp. 1055-1061
    • Doerge, D.R.1    Chirchwell, M.I.2    Marques, M.M.3    Beland, F.A.4
  • 21
    • 0035387450 scopus 로고    scopus 로고
    • Quantification of the Heterocyclic Aromatic Amine DNA Adduct N-(deoxyguanosin-8-yl)-2-amino-3-methylimidazo[4,5-f]quinoline in Livers of Rats Using Capillary Liquid Chromatography/Microelectrospray Mass Spectrometry: A Dose-Response Study
    • Soglia J.R., Turesky R.J., Paehler A., and Vouros P. Quantification of the Heterocyclic Aromatic Amine DNA Adduct N-(deoxyguanosin-8-yl)-2-amino-3-methylimidazo[4,5-f]quinoline in Livers of Rats Using Capillary Liquid Chromatography/Microelectrospray Mass Spectrometry: A Dose-Response Study. Anal. Chem 73 (2001) 2819
    • (2001) Anal. Chem , vol.73 , pp. 2819
    • Soglia, J.R.1    Turesky, R.J.2    Paehler, A.3    Vouros, P.4
  • 22
    • 0036230167 scopus 로고    scopus 로고
    • Analysis and Quantification of DNA Adducts of 2-Amino-3,8-dimethylimidazo[4,5-f]quinoxaline in Liver of Rats by Liquid Chromatography/Electrospray Tandem Mass Spectrometry
    • Paehler A., Richoz J., Soglia J., Vourous P., and Turesky R.J. Analysis and Quantification of DNA Adducts of 2-Amino-3,8-dimethylimidazo[4,5-f]quinoxaline in Liver of Rats by Liquid Chromatography/Electrospray Tandem Mass Spectrometry. Chem. Res. Toxicol 15 (2002) 551-561
    • (2002) Chem. Res. Toxicol , vol.15 , pp. 551-561
    • Paehler, A.1    Richoz, J.2    Soglia, J.3    Vourous, P.4    Turesky, R.J.5
  • 26
    • 0023951213 scopus 로고
    • Applications of NMR Spectroscopy to Studies of Reactive Intermediates and Their Interactions with Nucleic Acids
    • Harris T.M., Stone M.P., and Harris C.M. Applications of NMR Spectroscopy to Studies of Reactive Intermediates and Their Interactions with Nucleic Acids. Chem. Res. Toxicol 1 (1988) 79-96
    • (1988) Chem. Res. Toxicol , vol.1 , pp. 79-96
    • Harris, T.M.1    Stone, M.P.2    Harris, C.M.3
  • 27
    • 0003074918 scopus 로고
    • Covalent Nucleoside Adducts of Benzo[A]pyrene 7,8-Diol 9,10-eposide-Structural Reinvestigation and Characterization of a Novel Adenosine Adduct on the Ribose Moiety
    • Sayer J.M., Chadha A., Agarwal S.K., Yeh H.J., Yagi H., and Jerina D.M. Covalent Nucleoside Adducts of Benzo[A]pyrene 7,8-Diol 9,10-eposide-Structural Reinvestigation and Characterization of a Novel Adenosine Adduct on the Ribose Moiety. J. Org. Chem 56 (1991) 20-29
    • (1991) J. Org. Chem , vol.56 , pp. 20-29
    • Sayer, J.M.1    Chadha, A.2    Agarwal, S.K.3    Yeh, H.J.4    Yagi, H.5    Jerina, D.M.6
  • 28
    • 0022644069 scopus 로고
    • Identification and Mutagenicity of Metabolites of Aristolochic Acid Formed by Rat Liver
    • Schmeiser H.H., Pool B.L., and Wiessler M. Identification and Mutagenicity of Metabolites of Aristolochic Acid Formed by Rat Liver. Carcinogenesis 7 (1986) 59-63
    • (1986) Carcinogenesis , vol.7 , pp. 59-63
    • Schmeiser, H.H.1    Pool, B.L.2    Wiessler, M.3
  • 29
    • 33646948289 scopus 로고    scopus 로고
    • Study of the Phase I and Phase II Metabolism of Nephrotoxin Aristolochic Acid by Liquid Chromatography Tandem Mass Spectrometry
    • Chan W., Cui L., Xu G.W., and Cai Z.W. Study of the Phase I and Phase II Metabolism of Nephrotoxin Aristolochic Acid by Liquid Chromatography Tandem Mass Spectrometry. Rapid Commun. Mass Spectrom 20 (2006) 1755-1760
    • (2006) Rapid Commun. Mass Spectrom , vol.20 , pp. 1755-1760
    • Chan, W.1    Cui, L.2    Xu, G.W.3    Cai, Z.W.4
  • 30
    • 0029084490 scopus 로고
    • Characterization of Endogenous DNA-Adducts by Liquid-chromatography Electrospray-Ionization Tandem Mass Spectrometry
    • Chaudhary A.K., Nokubo M., Oglesby T.D., Marnett L.J., and Blair I.A. Characterization of Endogenous DNA-Adducts by Liquid-chromatography Electrospray-Ionization Tandem Mass Spectrometry. J. Mass Spectrom 30 (1995) 1157-1166
    • (1995) J. Mass Spectrom , vol.30 , pp. 1157-1166
    • Chaudhary, A.K.1    Nokubo, M.2    Oglesby, T.D.3    Marnett, L.J.4    Blair, I.A.5
  • 31
    • 4243116440 scopus 로고    scopus 로고
    • Synthesis and Liquid Chromatography/Tandem Mass Spectrometric Characterization of the Adducts of Bisphenol A o-Quinone with Glutathione and Nucleotide Monophosphates
    • Qiu S.X., Yang R.Z., and Gross M.L. Synthesis and Liquid Chromatography/Tandem Mass Spectrometric Characterization of the Adducts of Bisphenol A o-Quinone with Glutathione and Nucleotide Monophosphates. Chem. Res. Toxicol 17 (2004) 1038-1046
    • (2004) Chem. Res. Toxicol , vol.17 , pp. 1038-1046
    • Qiu, S.X.1    Yang, R.Z.2    Gross, M.L.3
  • 32
    • 0034662136 scopus 로고    scopus 로고
    • Liquid Chromatography/Electron Capture Atmospheric Pressure Chemical ionization/Mass Spectrometry: Analysis of Pentafluorobenzyl Derivatives of Biomolecules and Drugs in the Attomole Range
    • Singh G., Gutierrez A., Xu K.Y., and Blair I.A. Liquid Chromatography/Electron Capture Atmospheric Pressure Chemical ionization/Mass Spectrometry: Analysis of Pentafluorobenzyl Derivatives of Biomolecules and Drugs in the Attomole Range. Anal. Chem 72 (2000) 3007-3013
    • (2000) Anal. Chem , vol.72 , pp. 3007-3013
    • Singh, G.1    Gutierrez, A.2    Xu, K.Y.3    Blair, I.A.4
  • 33
    • 0002599739 scopus 로고
    • Four New Fluorescent Compounds Isolated from the Callus Tissue of Stephanica cepharantha
    • Akasu M., Hokwa H., and Fujita M. Four New Fluorescent Compounds Isolated from the Callus Tissue of Stephanica cepharantha. Tetrahedron Lett 41 (1974) 3609
    • (1974) Tetrahedron Lett , vol.41 , pp. 3609
    • Akasu, M.1    Hokwa, H.2    Fujita, M.3
  • 35
    • 0028881754 scopus 로고
    • Effect of Site-specifically Located Aristolochic Acid DNA Adducts on In Vitro DNA Synthesis by Human DNA Polymerase Alpha
    • Broschard T.H., Wiessler M., and Schmeiser H.H. Effect of Site-specifically Located Aristolochic Acid DNA Adducts on In Vitro DNA Synthesis by Human DNA Polymerase Alpha. Cancer Lett 98 (1995) 47-56
    • (1995) Cancer Lett , vol.98 , pp. 47-56
    • Broschard, T.H.1    Wiessler, M.2    Schmeiser, H.H.3
  • 36
    • 0033956126 scopus 로고    scopus 로고
    • Using Polymerase Arrest to Detect DNA Binding Specificity of Aristolochic Acid in the Mouse H-ras Gene
    • Arlt V.M., Wiessler M., and Schmeiser H.H. Using Polymerase Arrest to Detect DNA Binding Specificity of Aristolochic Acid in the Mouse H-ras Gene. Carcinogenesis 21 (2000) 235-242
    • (2000) Carcinogenesis , vol.21 , pp. 235-242
    • Arlt, V.M.1    Wiessler, M.2    Schmeiser, H.H.3
  • 37
    • 0035138584 scopus 로고    scopus 로고
    • Sequence-specific Detection of Aristolochic Acid-DNA Adducts in the Human p53 Gene by Terminal Transferase-dependent PCR
    • Arlt V.M., Schmeiser H.H., and Pfiefer G.P. Sequence-specific Detection of Aristolochic Acid-DNA Adducts in the Human p53 Gene by Terminal Transferase-dependent PCR. Carcinogenesis 22 (2001) 133-140
    • (2001) Carcinogenesis , vol.22 , pp. 133-140
    • Arlt, V.M.1    Schmeiser, H.H.2    Pfiefer, G.P.3
  • 38
    • 0037975592 scopus 로고    scopus 로고
    • Investigation of the Regio- and Stereo-selectivity of Deoxyguanosine Linkage to Deuterated 2-Hydroxyestradiol by Using Liquid Chromatography/ESI-Ion Trap Mass Spectrometry
    • Debrauwer L., Rathahao E., Jouanin I., Paris A., Clodic G., Molines H., Convert O., Fournier F., and Tabet J.C. Investigation of the Regio- and Stereo-selectivity of Deoxyguanosine Linkage to Deuterated 2-Hydroxyestradiol by Using Liquid Chromatography/ESI-Ion Trap Mass Spectrometry. J. Am. Soc. Mass Spectrom 14 (2003) 364-372
    • (2003) J. Am. Soc. Mass Spectrom , vol.14 , pp. 364-372
    • Debrauwer, L.1    Rathahao, E.2    Jouanin, I.3    Paris, A.4    Clodic, G.5    Molines, H.6    Convert, O.7    Fournier, F.8    Tabet, J.C.9


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.