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Volumn 531, Issue 1-2, 2003, Pages 5-23

Oxidative damage to DNA: Formation, measurement and biochemical features

Author keywords

Base lesions; Cyclonucleosides; DNA repair; Ionizing radiation; Mutagenesis; Oligonucleotide synthesis; One electron oxidation; Oxidized guanine; Tandem lesion; OH radical

Indexed keywords

8 HYDROXYGUANINE; CELL DNA; DNA; DNA GLYCOSYLTRANSFERASE; GUANINE; HYDROXYL RADICAL; MUTAGENIC AGENT; NUCLEOSIDE; OXYGEN; PURINE DERIVATIVE; PYRIMIDINE DERIVATIVE;

EID: 0344154463     PISSN: 00275107     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.mrfmmm.2003.09.001     Document Type: Conference Paper
Times cited : (632)

References (130)
  • 2
    • 4243545125 scopus 로고    scopus 로고
    • Oxidative nucleobase modifications leading to strand scission
    • Burrows C.J., Muller J.G. Oxidative nucleobase modifications leading to strand scission. Chem. Rev. 98:1998;1109-1152.
    • (1998) Chem. Rev. , vol.98 , pp. 1109-1152
    • Burrows, C.J.1    Muller, J.G.2
  • 5
    • 0034956662 scopus 로고    scopus 로고
    • Oxidative DNA damage, antioxidants and DNA repair: Applications of the comet assay
    • Collins A.R., Horvathova E. Oxidative DNA damage, antioxidants and DNA repair: applications of the comet assay. Biochem. Soc. Trans. 29:2001;337-341.
    • (2001) Biochem. Soc. Trans. , vol.29 , pp. 337-341
    • Collins, A.R.1    Horvathova, E.2
  • 6
    • 85030950380 scopus 로고    scopus 로고
    • Mutagenecity, toxicity and repair of DNA base damage induced by oxidation
    • S. Bjelland, E. Seeberg, Mutagenecity, toxicity and repair of DNA base damage induced by oxidation, Mutat. Res., this issue.
    • Mutat. Res. , Issue.THIS ISSUE
    • Bjelland, S.1    Seeberg, E.2
  • 7
    • 0027934952 scopus 로고
    • 2,2-Diamino-4-[(3,5-di-O-acetyl-2-deoxy-β-D-erythro-pentofuranosyl) amino]-5-(2H)-oxazolone: A novel and predominant radical oxidation product of 3′,5′-di-O-acetyl-2′-deoxyguanosine
    • Cadet J., Berger M., Buchko G.W., Josh P.C., Raoul S., Ravanat J.-L. 2,2-Diamino-4-[(3,5-di-O-acetyl-2-deoxy-β-D-erythro-pentofuranosyl)amino] -5-(2H)-oxazolone: A novel and predominant radical oxidation product of 3′,5′-di-O-acetyl-2′-deoxyguanosine. J. Am. Chem. Soc. 116:1994;7403-7404.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 7403-7404
    • Cadet, J.1    Berger, M.2    Buchko, G.W.3    Josh, P.C.4    Raoul, S.5    Ravanat, J.-L.6
  • 9
    • 0034602912 scopus 로고    scopus 로고
    • Reaction of HO· with guanine derivatives in aqueous solutions: Formation of two different redox-active OH adduct radicals and their unimolecular transformation reactions. Properties of G(-H)·
    • Candeias L.P., Steenken S. Reaction of HO· with guanine derivatives in aqueous solutions: formation of two different redox-active OH adduct radicals and their unimolecular transformation reactions. Properties of G(-H)· Chem. Eur. J. 6:2000;475-484.
    • (2000) Chem. Eur. J. , vol.6 , pp. 475-484
    • Candeias, L.P.1    Steenken, S.2
  • 11
    • 0032517343 scopus 로고    scopus 로고
    • Characterization and chemical stability of photooxidized oligonucleotides that contain 2,2-diamino-4-[(deoxy-β-D-erythro- pentofuranosyl)-amino]-5(2H)-oxazolone
    • Gasparutto D., Ravanat J.-L., Gérot O., Cadet J. Characterization and chemical stability of photooxidized oligonucleotides that contain 2,2-diamino-4-[(deoxy-β-D-erythro-pentofuranosyl)-amino]-5(2H)-oxazolone. J. Am. Chem. Soc. 120:1998;10283-10286.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 10283-10286
    • Gasparutto, D.1    Ravanat, J.-L.2    Gérot, O.3    Cadet, J.4
  • 12
    • 0032578191 scopus 로고    scopus 로고
    • Product analysis of GG-specific photooxidation of DNA via electron transfer: 2-aminoimidazolone as a major guanine oxidation product
    • Kino K., Saito I., Sugyiama H. Product analysis of GG-specific photooxidation of DNA via electron transfer: 2-aminoimidazolone as a major guanine oxidation product. J. Am. Chem. Soc. 120:1998;7373-7474.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 7373-7474
    • Kino, K.1    Saito, I.2    Sugyiama, H.3
  • 13
    • 0030066087 scopus 로고    scopus 로고
    • Guanine radical cations are precursors of 7,8-dihydro-8-oxo-2′- deoxyguanosine but are not precursors of immediate strand breaks in DNA
    • Cullis P.M., Malone M.E., Merson-Davies L.A. Guanine radical cations are precursors of 7,8-dihydro-8-oxo-2′-deoxyguanosine but are not precursors of immediate strand breaks in DNA. J. Am. Chem. Soc. 118:1996;2775-2781.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 2775-2781
    • Cullis, P.M.1    Malone, M.E.2    Merson-Davies, L.A.3
  • 14
    • 33748366270 scopus 로고
    • - and OH adducts
    • - and OH adducts. Chem. Rev. 89:1989;503-520.
    • (1989) Chem. Rev. , vol.89 , pp. 503-520
    • Steenken, S.1
  • 15
    • 0037467006 scopus 로고    scopus 로고
    • One-electron oxidation of the guanine moiety of 2′-deoxyguanosine: Influence of 8-oxo-7,8-dihydro-2′-deoxyguanosine
    • Ravanat J.-L., Saint-Pierre C., Cadet J. One-electron oxidation of the guanine moiety of 2′-deoxyguanosine: influence of 8-oxo-7,8-dihydro- 2′-deoxyguanosine. J. Am. Chem. Soc. 125:2003;2030-2031.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 2030-2031
    • Ravanat, J.-L.1    Saint-Pierre, C.2    Cadet, J.3
  • 16
    • 0032980386 scopus 로고    scopus 로고
    • Modification of DNA bases by photosensitized one-electron oxidation
    • Douki T., Cadet J. Modification of DNA bases by photosensitized one-electron oxidation. Int. J. Radiat. Biol. 75:1999;571-581.
    • (1999) Int. J. Radiat. Biol. , vol.75 , pp. 571-581
    • Douki, T.1    Cadet, J.2
  • 17
    • 0001309354 scopus 로고    scopus 로고
    • Hydroxyl radical-induced degradation of 2′-deoxyguanosine under reducing conditions
    • Douki T., Spinelli S., Ravanat J.-L., Cadet J. Hydroxyl radical-induced degradation of 2′-deoxyguanosine under reducing conditions. J. Chem. Soc. Perkin Trans. 2:1999;1875-1880.
    • (1999) J. Chem. Soc. Perkin Trans. , vol.2 , pp. 1875-1880
    • Douki, T.1    Spinelli, S.2    Ravanat, J.-L.3    Cadet, J.4
  • 18
    • 0035812375 scopus 로고    scopus 로고
    • 6-(2-deoxy- α,β-D-erythro-pentofuranosyl)-2,6-diamino-4-hydroxy-5- formamidopyrimidine)
    • 6-(2-deoxy-α,β-D-erythro-pentofuranosyl)-2,6- diamino-4-hydroxy-5-formamidopyrimidine). J. Am. Chem. Soc. 123:2001;8636-8637.
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 8636-8637
    • Haraguchi, K.1    Greenberg, M.M.2
  • 20
    • 0037012380 scopus 로고    scopus 로고
    • Synthesis and characterization of oligodeoxynucleotides containing formamidopyrimidine lesions and nonhydrolyzable analogues
    • Sambandam C.J., Hantosi Z., Greenberg M.M. Synthesis and characterization of oligodeoxynucleotides containing formamidopyrimidine lesions and nonhydrolyzable analogues. J. Am. Chem. Soc. 124:2002;3263-3269.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 3263-3269
    • Sambandam, C.J.1    Hantosi, Z.2    Greenberg, M.M.3
  • 21
    • 0037016581 scopus 로고    scopus 로고
    • Synthesis, stability, and conformation of the formamidopyrimidine G DNA lesion
    • Burgdorf L.T., Carell T. Synthesis, stability, and conformation of the formamidopyrimidine G DNA lesion. Chemistry. 8:2002;293-301.
    • (2002) Chemistry , vol.8 , pp. 293-301
    • Burgdorf, L.T.1    Carell, T.2
  • 22
    • 0042527365 scopus 로고    scopus 로고
    • Repair of DNA containing Fapy.dG and its β-C-nucleoside analogue by formamidopyrimidine DNA glycosylase and MutY
    • Wiederholt C.J., Delaney M.O., Pope M.A., Davies S.S., Greenberg M.M. Repair of DNA containing Fapy.dG and its β-C-nucleoside analogue by formamidopyrimidine DNA glycosylase and MutY. Biochemistry. 42:2003;9755-9760.
    • (2003) Biochemistry , vol.42 , pp. 9755-9760
    • Wiederholt, C.J.1    Delaney, M.O.2    Pope, M.A.3    Davies, S.S.4    Greenberg, M.M.5
  • 23
    • 0000267167 scopus 로고
    • Ionization of purine nucleosides and nucleotides and their components by 193-nm laser photolysis in aqueous solution: Model studies for oxidative damage of DNA
    • Candeias L.P., Steenken S. Ionization of purine nucleosides and nucleotides and their components by 193-nm laser photolysis in aqueous solution: model studies for oxidative damage of DNA. J. Am. Chem. Soc. 114:1992;699-704.
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 699-704
    • Candeias, L.P.1    Steenken, S.2
  • 24
    • 84877627020 scopus 로고
    • Photosensitized formation of 7,8-dihydro-8-oxo-2′-deoxyguanosine (8-hydroxy-2′-deoxyguanosine) in DNA by riboflavin: A non singlet oxygen mediated reaction
    • Kasai H., Yamaizumi Z., Berger M., Cadet J. Photosensitized formation of 7,8-dihydro-8-oxo-2′-deoxyguanosine (8-hydroxy-2′-deoxyguanosine) in DNA by riboflavin: a non singlet oxygen mediated reaction. J. Am. Chem. Soc. 114:1992;9692-9694.
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 9692-9694
    • Kasai, H.1    Yamaizumi, Z.2    Berger, M.3    Cadet, J.4
  • 25
    • 0037205867 scopus 로고    scopus 로고
    • Effect of hydration on the induction of strand breaks and base lesions in plasmid DNA films by gamma-radiation
    • Yokoya A., Cunniffe S.M., O'Neill P. Effect of hydration on the induction of strand breaks and base lesions in plasmid DNA films by gamma-radiation. J. Am. Chem. Soc. 124:2002;8859-8866.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 8859-8866
    • Yokoya, A.1    Cunniffe, S.M.2    O'Neill, P.3
  • 26
    • 0031587452 scopus 로고    scopus 로고
    • High-intensity UV laser photolysis of DNA and purine 2′- deoxyribonucleosides: Formation of 8-oxopurine damage and oligonucleotide strand cleavage as revealed by HPLC and gel electrophoresis studies
    • Angelov D., Spassky A., Berger M., Cadet J. High-intensity UV laser photolysis of DNA and purine 2′-deoxyribonucleosides: formation of 8-oxopurine damage and oligonucleotide strand cleavage as revealed by HPLC and gel electrophoresis studies. J. Am. Chem. Soc. 119:1997;11373-11380.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 11373-11380
    • Angelov, D.1    Spassky, A.2    Berger, M.3    Cadet, J.4
  • 27
    • 0035930027 scopus 로고    scopus 로고
    • UV laser photolysis of DNA: Effect of duplex stability on charge-transfer efficiency
    • Douki T., Angelov D., Cadet J. UV laser photolysis of DNA: effect of duplex stability on charge-transfer efficiency. J. Am. Chem. Soc. 123:2001;11360-11366.
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 11360-11366
    • Douki, T.1    Angelov, D.2    Cadet, J.3
  • 28
    • 0035822186 scopus 로고    scopus 로고
    • Guanine modifications following ionization of DNA occurs predominantly via intra- and not interstrand charge migration: An experimental and theoretical study
    • O'Neill P., Parker A.W., Plumb M.A., Siebbeles L.D.A. Guanine modifications following ionization of DNA occurs predominantly via intra- and not interstrand charge migration: an experimental and theoretical study. J. Phys. Chem. B. 105:2001;5283-5290.
    • (2001) J. Phys. Chem. B , vol.105 , pp. 5283-5290
    • O'Neill, P.1    Parker, A.W.2    Plumb, M.A.3    Siebbeles, L.D.A.4
  • 29
    • 0031024549 scopus 로고    scopus 로고
    • Photoinduced hydroxylation of deoxyguanosine in DNA by pterins: Sequence specificity and mechanism
    • Ito K., Kawanishi S. Photoinduced hydroxylation of deoxyguanosine in DNA by pterins: sequence specificity and mechanism. Biochemistry. 36:1997;1774-1781.
    • (1997) Biochemistry , vol.36 , pp. 1774-1781
    • Ito, K.1    Kawanishi, S.2
  • 30
    • 0034607422 scopus 로고    scopus 로고
    • Mapping of highest occupied molecular orbitals of duplex DNA by cobalt-mediated guanine oxidation
    • Saito I., Nakamura T., Nakatani K. Mapping of highest occupied molecular orbitals of duplex DNA by cobalt-mediated guanine oxidation. J. Am. Chem. Soc. 122:2000;3001-3006.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 3001-3006
    • Saito, I.1    Nakamura, T.2    Nakatani, K.3
  • 31
    • 0033928033 scopus 로고    scopus 로고
    • Radicals derived from histone hydroperoxides damage nucleobases in RNA and DNA
    • Luxford C., Dean R.T., Davies M.J. Radicals derived from histone hydroperoxides damage nucleobases in RNA and DNA. Chem. Res. Toxicol. 13:2000;665-672.
    • (2000) Chem. Res. Toxicol. , vol.13 , pp. 665-672
    • Luxford, C.1    Dean, R.T.2    Davies, M.J.3
  • 32
    • 0035816604 scopus 로고    scopus 로고
    • The carbonate radical is a site-selective oxidizing agent of guanine in double-stranded oligonucleotides
    • Shafirovich V., Dourandin A., Huang W., Geacintov N.E. The carbonate radical is a site-selective oxidizing agent of guanine in double-stranded oligonucleotides. J. Biol. Chem. 276:2001;24621-24626.
    • (2001) J. Biol. Chem. , vol.276 , pp. 24621-24626
    • Shafirovich, V.1    Dourandin, A.2    Huang, W.3    Geacintov, N.E.4
  • 34
    • 0031027125 scopus 로고    scopus 로고
    • How easily oxidizable is DNA? One-electron reduction potentials of adenosine and guanosine radicals in aqueous solutions
    • Steenken S., Jovanovic S.V. How easily oxidizable is DNA? One-electron reduction potentials of adenosine and guanosine radicals in aqueous solutions. J. Am. Chem. Soc. 119:1997;617-618.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 617-618
    • Steenken, S.1    Jovanovic, S.V.2
  • 35
    • 0037951371 scopus 로고    scopus 로고
    • Base sequence effects in radical cation migration in DNA: Support for the polaron-like hopping mechanism
    • Liu C.S., Schuster G.B. Base sequence effects in radical cation migration in DNA: support for the polaron-like hopping mechanism. J. Am. Chem. Soc. 125:2003;6098-6102.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 6098-6102
    • Liu, C.S.1    Schuster, G.B.2
  • 36
    • 0035997345 scopus 로고    scopus 로고
    • Long-distance electron transfer through DNA
    • Giese B. Long-distance electron transfer through DNA. Annu. Rev. Biochem. 71:2002;51-70.
    • (2002) Annu. Rev. Biochem. , vol.71 , pp. 51-70
    • Giese, B.1
  • 38
    • 0035913290 scopus 로고    scopus 로고
    • Direct observation of hole transfer through DNA by hopping between adenine bases and tunnelling
    • Giese B., Amaudrut J., Köhler A.-K., Spormann M., Wessely S. Direct observation of hole transfer through DNA by hopping between adenine bases and tunnelling. Nature. 412:2001;318-320.
    • (2001) Nature , vol.412 , pp. 318-320
    • Giese, B.1    Amaudrut, J.2    Köhler, A.-K.3    Spormann, M.4    Wessely, S.5
  • 39
    • 0001403207 scopus 로고    scopus 로고
    • Long-distance charge transport through DNA: Quantification and extension of the hopping model
    • Giese B., Spichty M. Long-distance charge transport through DNA: quantification and extension of the hopping model. Chem. Phys. Chem. 1:2000;195-198.
    • (2000) Chem. Phys. Chem. , vol.1 , pp. 195-198
    • Giese, B.1    Spichty, M.2
  • 40
    • 0027134597 scopus 로고
    • Endoperoxide formation in a guanosine derivative
    • Sheu C., Foote C.S. Endoperoxide formation in a guanosine derivative. J. Am. Chem. Soc. 115:1993;10446-10447.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 10446-10447
    • Sheu, C.1    Foote, C.S.2
  • 41
    • 0028927763 scopus 로고
    • Reaction of singlet oxygen with 2′-deoxyguanosine and DNA. Identification and characterization of the main oxidation products
    • Ravanat J.-L., Cadet J. Reaction of singlet oxygen with 2′-deoxyguanosine and DNA. Identification and characterization of the main oxidation products. Chem. Res. Toxicol. 8:1995;379-388.
    • (1995) Chem. Res. Toxicol. , vol.8 , pp. 379-388
    • Ravanat, J.-L.1    Cadet, J.2
  • 42
    • 0035810395 scopus 로고    scopus 로고
    • Spiroiminodihydantoin is the major product of 8-oxo-7,8-dihydroguanosine reaction with peroxynitrite in the presence of thiols and guanosine photooxidation by methylene blue
    • Niles J.C., Wishnok J.S., Tannenbaum S.R. Spiroiminodihydantoin is the major product of 8-oxo-7,8-dihydroguanosine reaction with peroxynitrite in the presence of thiols and guanosine photooxidation by methylene blue. Org. Lett. 3:2001;963-966.
    • (2001) Org. Lett. , vol.3 , pp. 963-966
    • Niles, J.C.1    Wishnok, J.S.2    Tannenbaum, S.R.3
  • 43
    • 0037149068 scopus 로고    scopus 로고
    • Spiroiminodihydantoin is a major product in the photooxidation of 2′-deoxyguanosine by the triplet states and oxyl radicals generated from hydroxyacetophenone photolysis and dioxetane thermolysis
    • Adam W., Arnold M.A., Grüne M., Nau W.M., Pischel U., Saha-Möller C.R. Spiroiminodihydantoin is a major product in the photooxidation of 2′-deoxyguanosine by the triplet states and oxyl radicals generated from hydroxyacetophenone photolysis and dioxetane thermolysis. Org. Lett. 4:2002;537-540.
    • (2002) Org. Lett. , vol.4 , pp. 537-540
    • Adam, W.1    Arnold, M.A.2    Grüne, M.3    Nau, W.M.4    Pischel, U.5    Saha-Möller, C.R.6
  • 44
    • 0033555373 scopus 로고    scopus 로고
    • Insertion of dGMP and dAMP during in vitro DNA synthesis opposite an oxidized form of 7,8-dihydro-8-oxoguanine
    • Duarte V., Muller J.G., Burrows C.J. Insertion of dGMP and dAMP during in vitro DNA synthesis opposite an oxidized form of 7,8-dihydro-8-oxoguanine. Nucleic Acids Res. 27:1999;496-502.
    • (1999) Nucleic Acids Res. , vol.27 , pp. 496-502
    • Duarte, V.1    Muller, J.G.2    Burrows, C.J.3
  • 45
    • 0033938243 scopus 로고    scopus 로고
    • Singlet oxygen DNA damage products: Formation and measurement
    • Cadet J., Douki T., Pouget J.-P., Ravanat J.-L. Singlet oxygen DNA damage products: formation and measurement. Methods Enzymol. 319:2000;143-153.
    • (2000) Methods Enzymol. , vol.319 , pp. 143-153
    • Cadet, J.1    Douki, T.2    Pouget, J.-P.3    Ravanat, J.-L.4
  • 48
    • 0037123284 scopus 로고    scopus 로고
    • Low-temperature photosensitized oxidation of a guanosine derivative and formation of an imidazole ring-opened product
    • Sheu C., Kang P., Khan S., Foote C.S. Low-temperature photosensitized oxidation of a guanosine derivative and formation of an imidazole ring-opened product. J. Am. Chem. Soc. 124:2002;3905-3913.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 3905-3913
    • Sheu, C.1    Kang, P.2    Khan, S.3    Foote, C.S.4
  • 49
    • 0026533905 scopus 로고
    • Substrate specificity of the Escherichia coli Fpg protein (formamidopyrimidine-DNA glycosylase): Excision of purine lesions in DNA produced by ionizing radiation and photosensitization
    • Boiteux S., Gajewski E., Laval J., Dizdaroglu M. Substrate specificity of the Escherichia coli Fpg protein (formamidopyrimidine-DNA glycosylase): excision of purine lesions in DNA produced by ionizing radiation and photosensitization. Biochemistry. 31:1992;106-110.
    • (1992) Biochemistry , vol.31 , pp. 106-110
    • Boiteux, S.1    Gajewski, E.2    Laval, J.3    Dizdaroglu, M.4
  • 50
    • 0037324821 scopus 로고    scopus 로고
    • Hydroxyl radical is not the main reactive species involved in the degradation of DNA bases by copper in the presence of hydrogen peroxide
    • Frelon S., Douki T., Favier A., Cadet J. Hydroxyl radical is not the main reactive species involved in the degradation of DNA bases by copper in the presence of hydrogen peroxide. Chem. Res. Toxicol. 16:2003;191-197.
    • (2003) Chem. Res. Toxicol. , vol.16 , pp. 191-197
    • Frelon, S.1    Douki, T.2    Favier, A.3    Cadet, J.4
  • 51
    • 0027973491 scopus 로고
    • The complexity of DNA damage: Relevance to biological consequences
    • Ward J.F. The complexity of DNA damage: relevance to biological consequences. Int. J. Radiat. Biol. 66:1994;427-432.
    • (1994) Int. J. Radiat. Biol. , vol.66 , pp. 427-432
    • Ward, J.F.1
  • 53
    • 0034678995 scopus 로고    scopus 로고
    • Tandem base lesions are generated by hydroxyl radical within isolated DNA in aerated aqueous solution
    • Bourdat A.-G., Douki T., Frelon S., Gasparutto D., Cadet J. Tandem base lesions are generated by hydroxyl radical within isolated DNA in aerated aqueous solution. J. Am. Chem. Soc. 122:2000;4549-4556.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 4549-4556
    • Bourdat, A.-G.1    Douki, T.2    Frelon, S.3    Gasparutto, D.4    Cadet, J.5
  • 54
    • 0036129039 scopus 로고    scopus 로고
    • DNA tandem lesions containing 8-oxo-7,8-dihydro-2′-deoxyguanosine and formamido residues arise from intramolecular addition of thymine peroxyl radical to guanine
    • Douki T., Rivière J., Cadet J. DNA tandem lesions containing 8-oxo-7,8-dihydro-2′-deoxyguanosine and formamido residues arise from intramolecular addition of thymine peroxyl radical to guanine. Chem. Res. Toxicol. 15:2002;445-454.
    • (2002) Chem. Res. Toxicol. , vol.15 , pp. 445-454
    • Douki, T.1    Rivière, J.2    Cadet, J.3
  • 55
    • 0034689864 scopus 로고    scopus 로고
    • Synthesis and UV photolysis of oligodeoxynucleotides that contain 5-(phenylthiomethyl)-2′-deoxyuridine: A specific photolabile precursor of 5-(2′-deoxyuridilyl)methyl radical
    • Romieu A., Bellon S., Gasparutto D., Cadet J. Synthesis and UV photolysis of oligodeoxynucleotides that contain 5-(phenylthiomethyl)-2′- deoxyuridine: a specific photolabile precursor of 5-(2′-deoxyuridilyl) methyl radical. Org. Lett. 2:2000;1085-1088.
    • (2000) Org. Lett. , vol.2 , pp. 1085-1088
    • Romieu, A.1    Bellon, S.2    Gasparutto, D.3    Cadet, J.4
  • 56
    • 0036229483 scopus 로고    scopus 로고
    • Cross-linked thymine-purine base tandem lesions: Synthesis, characterization, and measurement in gamma-irradiated isolated DNA
    • Bellon S., Ravanat J.-L., Gasparutto D., Cadet J. Cross-linked thymine-purine base tandem lesions: synthesis, characterization, and measurement in gamma-irradiated isolated DNA. Chem. Res. Toxicol. 15:2002;598-606.
    • (2002) Chem. Res. Toxicol. , vol.15 , pp. 598-606
    • Bellon, S.1    Ravanat, J.-L.2    Gasparutto, D.3    Cadet, J.4
  • 57
    • 0028812702 scopus 로고
    • Photosensitized oxygenation of a 7,8-dihydro-8-oxoguanosine derivative. Formation of dioxetane and hydroperoxide intermediates
    • Sheu C., Foote C.S. Photosensitized oxygenation of a 7,8-dihydro-8- oxoguanosine derivative. Formation of dioxetane and hydroperoxide intermediates. J. Am. Chem. Soc. 117:1995;474-477.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 474-477
    • Sheu, C.1    Foote, C.S.2
  • 58
    • 0032481373 scopus 로고    scopus 로고
    • Effects of guanine stacking on the oxidation of 8-oxoguanine in β-DNA
    • Prat F., Houk K.N., Foote C.S. Effects of guanine stacking on the oxidation of 8-oxoguanine in β-DNA. J. Am. Chem. Soc. 120:1998;845-846.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 845-846
    • Prat, F.1    Houk, K.N.2    Foote, C.S.3
  • 59
    • 0029990148 scopus 로고    scopus 로고
    • Photosensitized reaction of 8-oxo-7,8-dihydro-2′-deoxyguanosine: Identification of 1-(2-deoxy β-D-erythro-pentofuranosyl)-cyanuric acid as the major singlet oxidation product
    • Raoul S., Cadet J. Photosensitized reaction of 8-oxo-7,8-dihydro- 2′-deoxyguanosine: identification of 1-(2-deoxy β-D-erythro- pentofuranosyl)-cyanuric acid as the major singlet oxidation product. J. Am. Chem. Soc. 118:1996;1898-1982.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 1898-1982
    • Raoul, S.1    Cadet, J.2
  • 60
    • 0036012746 scopus 로고    scopus 로고
    • 18O ]-labeled singlet oxygen as a tool for mechanistic studies of 8-oxo-7,8-dihydroguanine oxidative damage: Detection of spiroiminodihydantoin, imidazolone and oxazolone derivatives
    • 18O ]-labeled singlet oxygen as a tool for mechanistic studies of 8-oxo-7,8-dihydroguanine oxidative damage: detection of spiroiminodihydantoin, imidazolone and oxazolone derivatives Biol. Chem. 383:2002;607-617.
    • (2002) Biol. Chem. , vol.383 , pp. 607-617
    • Martinez, G.R.1    Medeiros, M.H.2    Ravanat, J.-L.3    Cadet, J.4    Di Mascio, P.5
  • 61
    • 0035157221 scopus 로고    scopus 로고
    • Repair and mutagenic potential of oxaluric acid, a major product of singlet oxygen-mediated oxidation of 8-oxo-7,8-dihydroguanine
    • Duarte V., Gasparutto D., Jaquinod M., Ravanat J.-L., Cadet J. Repair and mutagenic potential of oxaluric acid, a major product of singlet oxygen-mediated oxidation of 8-oxo-7,8-dihydroguanine. Chem. Res. Toxicol. 114:2000;46-53.
    • (2000) Chem. Res. Toxicol. , vol.114 , pp. 46-53
    • Duarte, V.1    Gasparutto, D.2    Jaquinod, M.3    Ravanat, J.-L.4    Cadet, J.5
  • 62
    • 0034819860 scopus 로고    scopus 로고
    • Guanine oxidation: NMR characterization of a dehydro-guanidinohydantoin residue generated by a 2e-oxidation of d(GpT)
    • Chworos A., Coppel Y., Dubey I., Pratviel G., Meunier B. Guanine oxidation: NMR characterization of a dehydro-guanidinohydantoin residue generated by a 2e-oxidation of d(GpT). J. Am. Chem. Soc. 123:2001;5867-5877.
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 5867-5877
    • Chworos, A.1    Coppel, Y.2    Dubey, I.3    Pratviel, G.4    Meunier, B.5
  • 64
    • 0034932109 scopus 로고    scopus 로고
    • Characterization of hydantoin products from one-electron oxidation of 8-oxo-7,8-dihydroguanosine in a nucleoside model
    • Luo W., Muller J.G., Rachlin E.M., Burrows C.J. Characterization of hydantoin products from one-electron oxidation of 8-oxo-7,8-dihydroguanosine in a nucleoside model. Chem. Res. Toxicol. 14:2001;927-938.
    • (2001) Chem. Res. Toxicol. , vol.14 , pp. 927-938
    • Luo, W.1    Muller, J.G.2    Rachlin, E.M.3    Burrows, C.J.4
  • 65
    • 0034624588 scopus 로고    scopus 로고
    • Characterization of spiroiminodihydantoin as a product of one-electron oxidation of 8-oxo-7,8-dihydroguanosine
    • Luo W., Muller J.G., Rachlin E.M., Burrows C.J. Characterization of spiroiminodihydantoin as a product of one-electron oxidation of 8-oxo-7,8-dihydroguanosine. Org. Lett. 2:2000;613-616.
    • (2000) Org. Lett. , vol.2 , pp. 613-616
    • Luo, W.1    Muller, J.G.2    Rachlin, E.M.3    Burrows, C.J.4
  • 66
    • 0034814369 scopus 로고    scopus 로고
    • Direct oxidation of guanine and 7,8-dihydro-8-oxoguanine in DNA by a high-valent chromium complex: A possible mechanism for chromate genotoxicity
    • Sugden K.D., Campo C.K., Martin B.D. Direct oxidation of guanine and 7,8-dihydro-8-oxoguanine in DNA by a high-valent chromium complex: a possible mechanism for chromate genotoxicity. Chem. Res. Toxicol. 14:2001;1315-1322.
    • (2001) Chem. Res. Toxicol. , vol.14 , pp. 1315-1322
    • Sugden, K.D.1    Campo, C.K.2    Martin, B.D.3
  • 67
    • 0034486979 scopus 로고    scopus 로고
    • Peroxidase-catalyzed oxidative damage of DNA and 2′-deoxyguanosine by model compounds of lipid hydroperoxides: Involvement of peroxyl radicals
    • Adam W., Kurz A., Saha-Möller C.R. Peroxidase-catalyzed oxidative damage of DNA and 2′-deoxyguanosine by model compounds of lipid hydroperoxides: involvement of peroxyl radicals. Chem. Res. Toxicol. 13:2000;1199-1207.
    • (2000) Chem. Res. Toxicol. , vol.13 , pp. 1199-1207
    • Adam, W.1    Kurz, A.2    Saha-Möller, C.R.3
  • 68
    • 0037123204 scopus 로고    scopus 로고
    • A comparative photomechanistic study (spin trapping, EPR spectroscopy, transient kinetics, photoproducts) of nucleoside oxidation (dG and 8-oxodG) by triplet-excited acetophenones and by the radicals generated from α-oxy-substituted derivatives through Norrish-type I cleavage
    • Adam W., Arnold M.A., Nau W.M., Pischel U., Saha-Möller C.R. A comparative photomechanistic study (spin trapping, EPR spectroscopy, transient kinetics, photoproducts) of nucleoside oxidation (dG and 8-oxodG) by triplet-excited acetophenones and by the radicals generated from α-oxy-substituted derivatives through Norrish-type I cleavage. J. Am. Chem. Soc. 124:2002;3893-3904.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 3893-3904
    • Adam, W.1    Arnold, M.A.2    Nau, W.M.3    Pischel, U.4    Saha-Möller, C.R.5
  • 69
    • 0032576130 scopus 로고    scopus 로고
    • 7,8-Dihydro-8-oxo-2′-deoxyguanosine residues in DNA are radiation damage 'hot' spots in the direct γ radiation damage pathway
    • Doddridge A.Z., Cullis P.M., Jones G.D.D., Malone M.E. 7,8-Dihydro-8-oxo-2′-deoxyguanosine residues in DNA are radiation damage 'hot' spots in the direct γ radiation damage pathway. J. Am. Chem. Soc. 120:1998;10998-10999.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 10998-10999
    • Doddridge, A.Z.1    Cullis, P.M.2    Jones, G.D.D.3    Malone, M.E.4
  • 70
    • 0035817980 scopus 로고    scopus 로고
    • The pH-dependent role of superoxide in riboflavin-catalyzed photooxidation of 8-oxo-7,8-dihydroguanosine
    • Luo W., Muller J.G., Burrows C.J. The pH-dependent role of superoxide in riboflavin-catalyzed photooxidation of 8-oxo-7,8-dihydroguanosine. Org. Lett. 3:2001;2801-2804.
    • (2001) Org. Lett. , vol.3 , pp. 2801-2804
    • Luo, W.1    Muller, J.G.2    Burrows, C.J.3
  • 71
    • 0034610403 scopus 로고    scopus 로고
    • Removal of hydantoin products of 8-oxoguanine oxidation by the Escherichia coli DNA repair enzyme, FPG
    • Leopold M.D., Muller J.G., Burrows C.J., David S.S. Removal of hydantoin products of 8-oxoguanine oxidation by the Escherichia coli DNA repair enzyme, FPG. Biochemistry. 39:2000;14984-14992.
    • (2000) Biochemistry , vol.39 , pp. 14984-14992
    • Leopold, M.D.1    Muller, J.G.2    Burrows, C.J.3    David, S.S.4
  • 72
    • 0035339684 scopus 로고    scopus 로고
    • Repair of hydantoins, one electron oxidation product of 8-oxoguanine, by DNA glycosylases of Escherichia coli
    • Hazra T.K., Muller J.G., Manuel R.C., Burrows C.J., Lloyd R.S., Mitra S. Repair of hydantoins, one electron oxidation product of 8-oxoguanine, by DNA glycosylases of Escherichia coli. Nucleic Acids Res. 29:2001;1967-1974.
    • (2001) Nucleic Acids Res. , vol.29 , pp. 1967-1974
    • Hazra, T.K.1    Muller, J.G.2    Manuel, R.C.3    Burrows, C.J.4    Lloyd, R.S.5    Mitra, S.6
  • 73
    • 0037168491 scopus 로고    scopus 로고
    • In vitro nucleotide misinsertion opposite the oxidized guanosine lesions spiroiminodihydantoin and guanidinohydantoin and DNA synthesis past the lesions using Escherichia coli DNA polymerase I (Klenow fragment)
    • Komyushyna O., Berges A.M., Muller J.G., Burrows C.J. In vitro nucleotide misinsertion opposite the oxidized guanosine lesions spiroiminodihydantoin and guanidinohydantoin and DNA synthesis past the lesions using Escherichia coli DNA polymerase I (Klenow fragment). Biochemistry. 41:2002;15304-15314.
    • (2002) Biochemistry , vol.41 , pp. 15304-15314
    • Komyushyna, O.1    Berges, A.M.2    Muller, J.G.3    Burrows, C.J.4
  • 75
    • 0034653650 scopus 로고    scopus 로고
    • The trap depth (in DNA) of 8-oxo-7,8-dihydro-2′-deoxyguansoine as derived from electron transfer equilibria in aqueous solution
    • Steenken S., Jovanovic S.V., Bietti M., Bernhard K. The trap depth (in DNA) of 8-oxo-7,8-dihydro-2′-deoxyguansoine as derived from electron transfer equilibria in aqueous solution. J. Am. Chem. Soc. 122:2000;2373-2374.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 2373-2374
    • Steenken, S.1    Jovanovic, S.V.2    Bietti, M.3    Bernhard, K.4
  • 76
    • 0033552260 scopus 로고    scopus 로고
    • Sequence and stacking dependence of 8-oxoG oxidation: Comparison of one-electron vs. singlet oxygen mechanisms
    • Hickerson R.P., Prat F., Muller J.G., Foote C.S., Burrows C.J. Sequence and stacking dependence of 8-oxoG oxidation: comparison of one-electron vs. singlet oxygen mechanisms. J. Am. Chem. Soc. 121:1999;9423-9428.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 9423-9428
    • Hickerson, R.P.1    Prat, F.2    Muller, J.G.3    Foote, C.S.4    Burrows, C.J.5
  • 77
    • 0035131362 scopus 로고    scopus 로고
    • Direct spectroscopic observation of 8-oxo-7,8-dihydro-2′- deoxyguanosine radicals in double-stranded DNA generated by one-electron oxidation at a distance by 2-aminopurine radicals
    • Shafirovich V., Cadet J., Gasparutto D., Dourandin A., Huang W., Geacintov N.E. Direct spectroscopic observation of 8-oxo-7,8-dihydro-2′- deoxyguanosine radicals in double-stranded DNA generated by one-electron oxidation at a distance by 2-aminopurine radicals. J. Phys. Chem. B. 105:2001;586-592.
    • (2001) J. Phys. Chem. B , vol.105 , pp. 586-592
    • Shafirovich, V.1    Cadet, J.2    Gasparutto, D.3    Dourandin, A.4    Huang, W.5    Geacintov, N.E.6
  • 78
    • 0033914329 scopus 로고    scopus 로고
    • Peroxynitrite-induced secondary oxidative lesions at guanine nucleobases: Chemical stability and recognition by the Fpg DNA repair enzyme
    • Tretyakova N.Y., Wishnok J.S., Tannenbaum S.R. Peroxynitrite-induced secondary oxidative lesions at guanine nucleobases: chemical stability and recognition by the Fpg DNA repair enzyme. Chem. Res. Toxicol. 13:2000;658-664.
    • (2000) Chem. Res. Toxicol. , vol.13 , pp. 658-664
    • Tretyakova, N.Y.1    Wishnok, J.S.2    Tannenbaum, S.R.3
  • 80
    • 0036521853 scopus 로고    scopus 로고
    • Inter-laboratory validation of procedures for measuring 8-oxo-7,8-dihydroguanine/8-oxo-7,8-dihydro-2′-deoxyguanosine in DNA
    • ESCODD, Inter-laboratory validation of procedures for measuring 8-oxo-7,8-dihydroguanine/8-oxo-7,8-dihydro-2′-deoxyguanosine in DNA, Free Radic. Res. 36 (2002) 239-245.
    • (2002) Free Radic. Res. , vol.36 , pp. 239-245
  • 81
    • 0036605773 scopus 로고    scopus 로고
    • Comparison of results from different laboratories in measuring 8-oxo-2′-deoxyguanosine in synthetic oligonucleotides
    • B. Ris, ESCODD, Comparison of results from different laboratories in measuring 8-oxo-2′-deoxyguanosine in synthetic oligonucleotides, Free Radic. Res. 36 (2002) 649-659.
    • (2002) Free Radic. Res. , vol.36 , pp. 649-659
    • Ris, B.1
  • 82
    • 0036955299 scopus 로고    scopus 로고
    • Comparative analysis of baseline 8-oxo-7,8-dihydroguanine in mammalian cell DNA, by different methods in different laboratories: An approach consensus
    • ESCODD, Comparative analysis of baseline 8-oxo-7,8-dihydroguanine in mammalian cell DNA, by different methods in different laboratories: an approach consensus, Carcinogenesis 23 (2002) 2129-2133.
    • (2002) Carcinogenesis , vol.23 , pp. 2129-2133
  • 83
    • 0037446180 scopus 로고    scopus 로고
    • Measurement of DNA oxidation in human cells by chromatographic and enzymic methods
    • ESCODD, Measurement of DNA oxidation in human cells by chromatographic and enzymic methods, Free Radic. Biol. Med. 34 (2003) 1089-1099.
    • (2003) Free Radic. Biol. Med. , vol.34 , pp. 1089-1099
  • 86
    • 0033792418 scopus 로고    scopus 로고
    • High performance liquid chromatography-tandem mass spectrometry measurement of radiation-induced base damage
    • Frelon S., Douki T., Ravanat J.-L., Pouget J.-P., Tornabene C., Cadet J. High performance liquid chromatography-tandem mass spectrometry measurement of radiation-induced base damage. Chem. Res. Toxicol. 13:2000;1002-1010.
    • (2000) Chem. Res. Toxicol. , vol.13 , pp. 1002-1010
    • Frelon, S.1    Douki, T.2    Ravanat, J.-L.3    Pouget, J.-P.4    Tornabene, C.5    Cadet, J.6
  • 88
    • 17744417519 scopus 로고    scopus 로고
    • Cellular background level of 8-oxo-7,8-dihydro-2′-deoxyguanosine: An isotope based method to evaluate artefactual oxidation of DNA during its extraction and subsequent work-up
    • Ravanat J.-L., Douki T., Duez P., Gremaud E., Herbert K., Hofer T., Lasserre L., Saint-Pierre C., Favier A., Cadet J. Cellular background level of 8-oxo-7,8-dihydro-2′-deoxyguanosine: an isotope based method to evaluate artefactual oxidation of DNA during its extraction and subsequent work-up. Carcinogenesis. 23:2002;1911-1918.
    • (2002) Carcinogenesis , vol.23 , pp. 1911-1918
    • Ravanat, J.-L.1    Douki, T.2    Duez, P.3    Gremaud, E.4    Herbert, K.5    Hofer, T.6    Lasserre, L.7    Saint-Pierre, C.8    Favier, A.9    Cadet, J.10
  • 94
    • 0028000266 scopus 로고
    • Oxidative DNA damage: Endonuclease fingerprint
    • Epe B., Hegler J. Oxidative DNA damage: endonuclease fingerprint. Methods Enzymol. 234:1994;122-1231.
    • (1994) Methods Enzymol. , vol.234 , pp. 122-1231
    • Epe, B.1    Hegler, J.2
  • 95
    • 0030297062 scopus 로고    scopus 로고
    • Sensitive analysis of oxidative DNA damage in mammalian cells: Use of the bacterial Fpg protein in combination with alkaline unwinding
    • Hartwig A., Dally H., Schlepegrell R. Sensitive analysis of oxidative DNA damage in mammalian cells: use of the bacterial Fpg protein in combination with alkaline unwinding. Toxicol. Lett. 88:1996;80-85.
    • (1996) Toxicol. Lett. , vol.88 , pp. 80-85
    • Hartwig, A.1    Dally, H.2    Schlepegrell, R.3
  • 96
    • 0036249832 scopus 로고    scopus 로고
    • Formation of modified DNA bases in cells exposed either to gamma radiation or to high-LET radiation
    • Pouget J.-P., Frelon S., Ravanat J.-L., Testard I., Odin F., Cadet J. Formation of modified DNA bases in cells exposed either to gamma radiation or to high-LET radiation. Radiat. Res. 157:2002;589-595.
    • (2002) Radiat. Res. , vol.157 , pp. 589-595
    • Pouget, J.-P.1    Frelon, S.2    Ravanat, J.-L.3    Testard, I.4    Odin, F.5    Cadet, J.6
  • 97
    • 0036589676 scopus 로고    scopus 로고
    • Radical oxidation of the adenine moiety of nucleoside and DNA: 2-hydroxy-2′-deoxyadenosine is a minor decomposition product
    • Frelon S., Douki T., Cadet J. Radical oxidation of the adenine moiety of nucleoside and DNA: 2-hydroxy-2′-deoxyadenosine is a minor decomposition product. Free Radic. Res. 36:2002;499-508.
    • (2002) Free Radic. Res. , vol.36 , pp. 499-508
    • Frelon, S.1    Douki, T.2    Cadet, J.3
  • 98
    • 0027960283 scopus 로고
    • Ionizing radiation causes greater DNA base damage in radiation-sensitive mutantM10 cells than in parent mouse lymphoma L5178Y cells
    • Mori T., Dizdaroglu M. Ionizing radiation causes greater DNA base damage in radiation-sensitive mutantM10 cells than in parent mouse lymphoma L5178Y cells. Radiat. Res. 140:1994;85-90.
    • (1994) Radiat. Res. , vol.140 , pp. 85-90
    • Mori, T.1    Dizdaroglu, M.2
  • 100
    • 0037163123 scopus 로고    scopus 로고
    • The Cockayne syndrome group B product is involved in cellular repair of 8-hydroxyadenine in DNA
    • Tuo J., Jaruga P., Rodriguez H., Dizdaroglu M., Bohr V.A. The Cockayne syndrome group B product is involved in cellular repair of 8-hydroxyadenine in DNA. J. Biol. Chem. 277:2002;30832-30837.
    • (2002) J. Biol. Chem. , vol.277 , pp. 30832-30837
    • Tuo, J.1    Jaruga, P.2    Rodriguez, H.3    Dizdaroglu, M.4    Bohr, V.A.5
  • 101
    • 0141869885 scopus 로고    scopus 로고
    • Primary fibroblasts of Cockayne syndrome patients are defective in cellular repair of 8-hydroguanine and 8-hydroxyadenine resulting from oxidative stress
    • Tuo J., Jaruga P., Rodriguez H., Bohr V.A., Dizdaroglu M. Primary fibroblasts of Cockayne syndrome patients are defective in cellular repair of 8-hydroguanine and 8-hydroxyadenine resulting from oxidative stress. FASEB J. 17:2003;668-674.
    • (2003) FASEB J. , vol.17 , pp. 668-674
    • Tuo, J.1    Jaruga, P.2    Rodriguez, H.3    Bohr, V.A.4    Dizdaroglu, M.5
  • 102
    • 0032960559 scopus 로고    scopus 로고
    • Measurement of DNA base damage in cells exposed to low doses of gamma radiation: Comparison between the HPLC-CD and the comet assays
    • Pouget J.-P., Ravanat J.-L., Douki T., Richard M.-J., Cadet J. Measurement of DNA base damage in cells exposed to low doses of gamma radiation: comparison between the HPLC-CD and the comet assays. Int. J. Radiat. Biol. 75:1999;51-58.
    • (1999) Int. J. Radiat. Biol. , vol.75 , pp. 51-58
    • Pouget, J.-P.1    Ravanat, J.-L.2    Douki, T.3    Richard, M.-J.4    Cadet, J.5
  • 103
    • 0033914527 scopus 로고    scopus 로고
    • DNA damage induced in cells by gamma and UVA radiations: Calibrated comet assay with HPLC/GC-MS and HPLC-EC
    • Pouget J.-P., Douki T., Richard M.-J., Cadet J. DNA damage induced in cells by gamma and UVA radiations: calibrated comet assay with HPLC/GC-MS and HPLC-EC. Chem. Res. Toxicol. 13:2000;541-547.
    • (2000) Chem. Res. Toxicol. , vol.13 , pp. 541-547
    • Pouget, J.-P.1    Douki, T.2    Richard, M.-J.3    Cadet, J.4
  • 104
    • 0034192265 scopus 로고    scopus 로고
    • The human OGG1 gene: Structure, functions, and its implication in the process of carcinogenesis
    • Boiteux S., Radicella J.P. The human OGG1 gene: structure, functions, and its implication in the process of carcinogenesis. Arch. Biochem. Biophys. 377:2000;1-8.
    • (2000) Arch. Biochem. Biophys. , vol.377 , pp. 1-8
    • Boiteux, S.1    Radicella, J.P.2
  • 106
    • 0033574208 scopus 로고    scopus 로고
    • Excision of 5,6-dihydroxy-5,6-dihydrothymine, 5,6-dihydrothymine and 5-hydroxycytosine from defined sequence oligonucleotides by Escherichia coli endonuclease III and Fpg proteins: Kinetic and mechanistic aspects
    • D'Ham C., Romieu A., Jaquinod M., Gasparutto D., Cadet J. Excision of 5,6-dihydroxy-5,6-dihydrothymine, 5,6-dihydrothymine and 5-hydroxycytosine from defined sequence oligonucleotides by Escherichia coli endonuclease III and Fpg proteins: kinetic and mechanistic aspects. Biochemistry. 38:1999;3335-3344.
    • (1999) Biochemistry , vol.38 , pp. 3335-3344
    • D'Ham, C.1    Romieu, A.2    Jaquinod, M.3    Gasparutto, D.4    Cadet, J.5
  • 107
    • 0033929846 scopus 로고    scopus 로고
    • Repair and coding properties of 5-hydroxy-5-methylhydantoin nucleoside inserted into DNA oligomers
    • Gasparutto D., Ait-Abbas M., Jaquinod M., Boiteux S., Cadet J. Repair and coding properties of 5-hydroxy-5-methylhydantoin nucleoside inserted into DNA oligomers. Chem. Res. Toxicol. 13:2000;575-584.
    • (2000) Chem. Res. Toxicol. , vol.13 , pp. 575-584
    • Gasparutto, D.1    Ait-Abbas, M.2    Jaquinod, M.3    Boiteux, S.4    Cadet, J.5
  • 108
    • 0034990220 scopus 로고    scopus 로고
    • *) diastereoisomers of 1-[2-deoxy-β-D-erythro- pentofuranosyl]-5-hydroxyhydantoin into oligodeoxyribonucleotides
    • *) diastereoisomers of 1-[2-deoxy-β-D-erythro-pentofuranosyl]-5-hydroxyhydantoin into oligodeoxyribonucleotides, Eur. J. Org. Chem. (2001) 2091-2099.
    • (2001) Eur. J. Org. Chem. , pp. 2091-2099
    • Muller, E.1    Gasparutto, D.2    Lebrun, E.3    Cadet, J.4
  • 109
    • 0034177417 scopus 로고    scopus 로고
    • In vitro DNA synthesis opposite oxazolone and repair of this DNA damage using modified oligonucleotides
    • Duarte V., Gasparutto D., Jaquinod M., Cadet J. In vitro DNA synthesis opposite oxazolone and repair of this DNA damage using modified oligonucleotides. Nucleic Acids Res. 28:2000;1555-1563.
    • (2000) Nucleic Acids Res. , vol.28 , pp. 1555-1563
    • Duarte, V.1    Gasparutto, D.2    Jaquinod, M.3    Cadet, J.4
  • 110
    • 0035157221 scopus 로고    scopus 로고
    • Repair and mutagenic potential of oxaluric acid, a major product of singlet oxygen-mediated oxidation of 8-oxo-7,8-dihydroguanine
    • Duarte V., Gasparutto D., Jaquinod M., Ravanat J.-L., Cadet J. Repair and mutagenic potential of oxaluric acid, a major product of singlet oxygen-mediated oxidation of 8-oxo-7,8-dihydroguanine. Chem. Res. Toxicol. 14:2001;46-53.
    • (2001) Chem. Res. Toxicol. , vol.14 , pp. 46-53
    • Duarte, V.1    Gasparutto, D.2    Jaquinod, M.3    Ravanat, J.-L.4    Cadet, J.5
  • 111
    • 0032839543 scopus 로고    scopus 로고
    • Synthesis and biochemical properties of cyanuric acid nucleoside containing DNA oligomers
    • Gasparutto D., Da Cruz S., Bourdat A.-G., Jaquinod M., Cadet J. Synthesis and biochemical properties of cyanuric acid nucleoside containing DNA oligomers. Chem. Res. Toxicol. 12:1999;630-638.
    • (1999) Chem. Res. Toxicol. , vol.12 , pp. 630-638
    • Gasparutto, D.1    Da Cruz, S.2    Bourdat, A.-G.3    Jaquinod, M.4    Cadet, J.5
  • 112
    • 0033557286 scopus 로고    scopus 로고
    • Synthesis and enzymatic processing of oligonucleotides containing tandem base damage
    • Bourdat A.-G., Gasparutto D., Cadet J. Synthesis and enzymatic processing of oligonucleotides containing tandem base damage. Nucleic Acids Res. 27:1999;1015-1024.
    • (1999) Nucleic Acids Res. , vol.27 , pp. 1015-1024
    • Bourdat, A.-G.1    Gasparutto, D.2    Cadet, J.3
  • 113
    • 0035873875 scopus 로고    scopus 로고
    • Recognition and kinetics for excision of a base lesion within clustered DNA damage by the Escherichia coli proteins Fpg and Nth
    • David-Cordonnier M.-H., Laval J., O'Neill P. Recognition and kinetics for excision of a base lesion within clustered DNA damage by the Escherichia coli proteins Fpg and Nth. Biochemistry. 40:2001;5738-5746.
    • (2001) Biochemistry , vol.40 , pp. 5738-5746
    • David-Cordonnier, M.-H.1    Laval, J.2    O'Neill, P.3
  • 114
    • 0035283041 scopus 로고    scopus 로고
    • Excision of 8-oxoguanine within clustered damage by the yeast OGG1 protein
    • David-Cordonnier M.-H., Boiteux S., O'Neill P. Excision of 8-oxoguanine within clustered damage by the yeast OGG1 protein. Nucleic Acids Res. 29:2001;1107-1113.
    • (2001) Nucleic Acids Res. , vol.29 , pp. 1107-1113
    • David-Cordonnier, M.-H.1    Boiteux, S.2    O'Neill, P.3
  • 115
    • 0034697371 scopus 로고    scopus 로고
    • Clustered DNA damage, influence on damage excision by XRS5 nuclear extracts and Escherichia coli Nth and Fpg proteins
    • David-Cordonnier M.-H., Laval J., O'Neill P. Clustered DNA damage, influence on damage excision by XRS5 nuclear extracts and Escherichia coli Nth and Fpg proteins. J. Biol. Chem. 275:2000;11865-11873.
    • (2000) J. Biol. Chem. , vol.275 , pp. 11865-11873
    • David-Cordonnier, M.-H.1    Laval, J.2    O'Neill, P.3
  • 116
    • 0035912756 scopus 로고    scopus 로고
    • Abortive base-excision repair of radiation-induced clustered DNA lesions in Escherichia coli
    • Blaisdell J.G., Wallace S.S. Abortive base-excision repair of radiation-induced clustered DNA lesions in Escherichia coli. Proc. Natl. Acad. Sci. U.S.A. 98:2001;7426-7430.
    • (2001) Proc. Natl. Acad. Sci. U.S.A. , vol.98 , pp. 7426-7430
    • Blaisdell, J.G.1    Wallace, S.S.2
  • 117
    • 0021957619 scopus 로고
    • Radiation-induced decomposition of the purine bases within DNA and related model compounds
    • Cadet J., Berger M. Radiation-induced decomposition of the purine bases within DNA and related model compounds. Int. J. Radiat. Biol. 47:1985;127-143.
    • (1985) Int. J. Radiat. Biol. , vol.47 , pp. 127-143
    • Cadet, J.1    Berger, M.2
  • 118
    • 0022518370 scopus 로고
    • Free-radical-induced formation of an 8,5′-cyclo-2′- deoxyguanosine moiety in deoxyribonucleic acid
    • Dizdaroglu M. Free-radical-induced formation of an 8,5′-cyclo- 2′-deoxyguanosine moiety in deoxyribonucleic acid. Biochem. J. 238:1986;247-254.
    • (1986) Biochem. J. , vol.238 , pp. 247-254
    • Dizdaroglu, M.1
  • 119
    • 0034636004 scopus 로고    scopus 로고
    • Removal of oxygen free-radical-induced 5′,8-purine cyclodeoxynucleosides from DNA by the nucleotide excision-repair pathway in human cells
    • Kuraoka I., Bender C., Romieu A., Cadet J., Wood R.D., Lindahl T. Removal of oxygen free-radical-induced 5′,8-purine cyclodeoxynucleosides from DNA by the nucleotide excision-repair pathway in human cells. Proc. Natl. Acad. Sci. U.S.A. 97:2000;3832-3837.
    • (2000) Proc. Natl. Acad. Sci. U.S.A. , vol.97 , pp. 3832-3837
    • Kuraoka, I.1    Bender, C.2    Romieu, A.3    Cadet, J.4    Wood, R.D.5    Lindahl, T.6
  • 121
    • 0000964269 scopus 로고    scopus 로고
    • Site-specific introduction of (5′S)-5′,8-cyclo-2′- deoxyadenosine into oligodeoxyribonucleotides
    • Romieu A., Gasparutto D., Molko D., Cadet J. Site-specific introduction of (5′S)-5′,8-cyclo-2′-deoxyadenosine into oligodeoxyribonucleotides. J. Org. Chem. 63:1998;5245-5249.
    • (1998) J. Org. Chem. , vol.63 , pp. 5245-5249
    • Romieu, A.1    Gasparutto, D.2    Molko, D.3    Cadet, J.4
  • 122
    • 0032782017 scopus 로고    scopus 로고
    • Synthesis and characterization of oligonucleotides containing 5′,8-cyclopurine 2′-deoxyribonucleosides: (5′R)-5′,8- cyclo-2′-deoxyadenosine, (5′S)-5′,8-cyclo-2′- deoxyguanosine, and (5′R)-5′,8-cyclo-2′-deoxyguanosine
    • Romieu A., Gasparutto D., Cadet J. Synthesis and characterization of oligonucleotides containing 5′,8-cyclopurine 2′- deoxyribonucleosides: (5′R)-5′,8-cyclo-2′-deoxyadenosine, (5′S)-5′,8-cyclo-2′-deoxyguanosine, and (5′R)-5′, 8-cyclo-2′-deoxyguanosine. Chem. Res. Toxicol. 12:1999;412-421.
    • (1999) Chem. Res. Toxicol. , vol.12 , pp. 412-421
    • Romieu, A.1    Gasparutto, D.2    Cadet, J.3
  • 123
    • 0034721685 scopus 로고    scopus 로고
    • Chemical and biochemical properties of oligonucleotides that contain (5′S,6S)-cyclo-5,6-dihydro-2′-deoxyuridine and (5′S,6S)-cyclo- 5,6-dihydrothymidine, two main radiation-induced degradation products of pyrimidine 2′-deoxyribonucleosides
    • Muller E., Gasparutto D., Jaquinod M., Romieu A., Cadet J. Chemical and biochemical properties of oligonucleotides that contain (5′S,6S)-cyclo-5, 6-dihydro-2′-deoxyuridine and (5′S,6S)-cyclo-5,6-dihydrothymidine, two main radiation-induced degradation products of pyrimidine 2′-deoxyribonucleosides. Tetrahedron. 56:2000;8689-8701.
    • (2000) Tetrahedron , vol.56 , pp. 8689-8701
    • Muller, E.1    Gasparutto, D.2    Jaquinod, M.3    Romieu, A.4    Cadet, J.5
  • 124
    • 0001383634 scopus 로고    scopus 로고
    • Synthesis and characterization of oligodeoxynucleotides containing the two 5R and 5S diastereomers of (5′S,6S)-5′,6-cyclo-5,6- dihydrothymidine, radiation-induced tandem lesions of thymidine
    • Romieu A., Gasparutto D., Cadet J. Synthesis and characterization of oligodeoxynucleotides containing the two 5R and 5S diastereomers of (5′S,6S)-5′,6-cyclo-5,6-dihydrothymidine, radiation-induced tandem lesions of thymidine. J. Chem. Soc. Perkin Trans. 1:1999;257-264.
    • (1999) J. Chem. Soc. Perkin Trans. , vol.1 , pp. 257-264
    • Romieu, A.1    Gasparutto, D.2    Cadet, J.3
  • 125
    • 0036903711 scopus 로고    scopus 로고
    • Chemical synthesis and biochemical properties of oligonucleotides that contain the (5′S,5S,6S)-5′,6-cyclo-5-hydroxy-5,6-dihydro-2′- deoxyuridine DNA lesion
    • Muller E., Gasparutto D., Cadet J. Chemical synthesis and biochemical properties of oligonucleotides that contain the (5′S,5S,6S)-5′,6- cyclo-5-hydroxy-5,6-dihydro-2′-deoxyuridine DNA lesion. ChemBioChem. 3:2002;534-542.
    • (2002) ChemBioChem. , vol.3 , pp. 534-542
    • Muller, E.1    Gasparutto, D.2    Cadet, J.3
  • 126
    • 0034691679 scopus 로고    scopus 로고
    • Mutation spectra induced by replication of two vicinal oxidative DNA lesions in mammalian cells
    • Gentil A., Le Page F., Cadet J., Sarasin A. Mutation spectra induced by replication of two vicinal oxidative DNA lesions in mammalian cells. Mutat. Res. 452:2000;51-56.
    • (2000) Mutat. Res. , vol.452 , pp. 51-56
    • Gentil, A.1    Le Page, F.2    Cadet, J.3    Sarasin, A.4
  • 127
    • 0033969864 scopus 로고    scopus 로고
    • Repair and replication of oxidized DNA bases using modified oligodeoxyribonucleotides
    • Gasparutto D., Bourdat A.-G., D'ham C., Duarte V., Romieu A., Cadet J. Repair and replication of oxidized DNA bases using modified oligodeoxyribonucleotides. Biochimie. 82:2000;19-24.
    • (2000) Biochimie , vol.82 , pp. 19-24
    • Gasparutto, D.1    Bourdat, A.-G.2    D'Ham, C.3    Duarte, V.4    Romieu, A.5    Cadet, J.6
  • 128
    • 0035966003 scopus 로고    scopus 로고
    • Oxygen free radical damage to DNA. Translesion synthesis by human DNA polymerase η and resistance to exonuclease action at cyclopurine deoxynucleoside residues
    • Kuraoka I., Robins P., Masutani C., Hanaoka F., Gasparutto D., Cadet J., Wood R.D., Lindahl T. Oxygen free radical damage to DNA. Translesion synthesis by human DNA polymerase η and resistance to exonuclease action at cyclopurine deoxynucleoside residues. J. Biol. Chem. 276:2001;49283-49288.
    • (2001) J. Biol. Chem. , vol.276 , pp. 49283-49288
    • Kuraoka, I.1    Robins, P.2    Masutani, C.3    Hanaoka, F.4    Gasparutto, D.5    Cadet, J.6    Wood, R.D.7    Lindahl, T.8
  • 129
    • 0029553649 scopus 로고
    • Chemical aspects of the benzophenone-photosensitized formation of two lysine-2′-deoxyguanosine cross-links
    • Morin B., Cadet J. Chemical aspects of the benzophenone-photosensitized formation of two lysine-2′-deoxyguanosine cross-links. J. Am. Chem. Soc. 117:1995;12408-12415.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 12408-12415
    • Morin, B.1    Cadet, J.2
  • 130
    • 0038799736 scopus 로고    scopus 로고
    • Oxidative DNA damage: Mechanisms, mutation, and disease
    • Cooke M.S., Evans M.D., Dizdaroglu M., Lunec J. Oxidative DNA damage: mechanisms, mutation, and disease. FASEB J. 17:2003;1195-1212.
    • (2003) FASEB J. , vol.17 , pp. 1195-1212
    • Cooke, M.S.1    Evans, M.D.2    Dizdaroglu, M.3    Lunec, J.4


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