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Volumn 82, Issue 5, 2006, Pages 1219-1225

Singlet oxygen oxidation of isolated and cellular DNA: Product formation and mechanistic insights

Author keywords

[No Author keywords available]

Indexed keywords

DNA; DRUG DERIVATIVE; GUANINE; GUANOSINE; NUCLEOSIDE; OLIGONUCLEOTIDE; SINGLET OXYGEN; SOLVENT;

EID: 33750718155     PISSN: 00318655     EISSN: None     Source Type: Journal    
DOI: 10.1562/2006-06-09-IR-914     Document Type: Conference Paper
Times cited : (163)

References (73)
  • 2
    • 0002204357 scopus 로고
    • (Edited by W. A. Prior) Academic Press, New York
    • Foote, C. S. (1976). In Free Radicals in Biology (Edited by W. A. Prior) pp. 85-133. Academic Press, New York.
    • (1976) Free Radicals in Biology , pp. 85-133
    • Foote, C.S.1
  • 6
    • 0030006313 scopus 로고    scopus 로고
    • Evidence for the photosensitized formation of singlet oxygen by UVB irradiation of 2′-deoxyguanosine 5′-monophosphate
    • Mohammad, T. and H. Morrison (1996) Evidence for the photosensitized formation of singlet oxygen by UVB irradiation of 2′-deoxyguanosine 5′-monophosphate. J. Am. Chem. Soc. 118, 1221-1222.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 1221-1222
    • Mohammad, T.1    Morrison, H.2
  • 7
    • 0038545400 scopus 로고    scopus 로고
    • Photooxidation of 2′-deoxyguanosine 5′-monophosphate in aqueous solution
    • Torum, L. and H. Morrison (2003) Photooxidation of 2′- deoxyguanosine 5′-monophosphate in aqueous solution. Photochem. Photobiol. 77, 370-375.
    • (2003) Photochem. Photobiol. , vol.77 , pp. 370-375
    • Torum, L.1    Morrison, H.2
  • 8
    • 29844434892 scopus 로고    scopus 로고
    • A new approach to measuring the action spectrum for singlet oxygen production by human retinal lipofuscin
    • Avalle, L. B., J. Dillon, S. Tari and E. R. Gaillard (2005) A new approach to measuring the action spectrum for singlet oxygen production by human retinal lipofuscin. Photochem. Photobiol. 81, 1347-1350.
    • (2005) Photochem. Photobiol. , vol.81 , pp. 1347-1350
    • Avalle, L.B.1    Dillon, J.2    Tari, S.3    Gaillard, E.R.4
  • 9
    • 0026762871 scopus 로고
    • Intracellular singlet oxygen generation by phagocytosing neutrophils in response to particles coated with a chemical trap
    • Steinbeck, M. J., A. U. Khan and M. J. Karnovsky (1992) Intracellular singlet oxygen generation by phagocytosing neutrophils in response to particles coated with a chemical trap. J. Biol. Chem. 267, 13425-13433.
    • (1992) J. Biol. Chem. , vol.267 , pp. 13425-13433
    • Steinbeck, M.J.1    Khan, A.U.2    Karnovsky, M.J.3
  • 12
    • 26444470448 scopus 로고    scopus 로고
    • Singlet-oxygen chemiluminescence in peroxide reactions
    • Adam, W., D. V. Kazakov and V. P. Kazakov (2005) Singlet-oxygen chemiluminescence in peroxide reactions. Chem. Rev. 105, 3371-3387.
    • (2005) Chem. Rev. , vol.105 , pp. 3371-3387
    • Adam, W.1    Kazakov, D.V.2    Kazakov, V.P.3
  • 13
    • 0038288716 scopus 로고    scopus 로고
    • Singlet molecular oxygen generated from lipid hydroperoxides by the Russell mechanism: Studies using 18(O)-labeled linoleic acid hydroperoxide and monomol light emission measurements
    • Miyamoto, S., G. R. Martinez, M. H. G. Medeiros and P. Di Mascio (2003) Singlet molecular oxygen generated from lipid hydroperoxides by the Russell mechanism: Studies using 18(O)-labeled linoleic acid hydroperoxide and monomol light emission measurements. J. Am. Chem. Soc. 125, 6172-6179.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 6172-6179
    • Miyamoto, S.1    Martinez, G.R.2    Medeiros, M.H.G.3    Di Mascio, P.4
  • 15
    • 31044456412 scopus 로고    scopus 로고
    • Linoleic acid hydroperoxide reacts with hypochlorous acid, generating peroxyl radical intermediates and singlet molecular oxygen
    • Miyamoto, S., G. R. Martinez, D. Rettori, O. Augusto, M. H. G. Medeiros and P. Di Mascio (2006) Linoleic acid hydroperoxide reacts with hypochlorous acid, generating peroxyl radical intermediates and singlet molecular oxygen. Proc. Natl. Acad. Sci. USA 103, 293-298.
    • (2006) Proc. Natl. Acad. Sci. USA , vol.103 , pp. 293-298
    • Miyamoto, S.1    Martinez, G.R.2    Rettori, D.3    Augusto, O.4    Medeiros, M.H.G.5    Di Mascio, P.6
  • 16
    • 27144523688 scopus 로고    scopus 로고
    • Subcellular, time-resolved studies of singlet oxygen in single cells
    • Snyder J. W., E. Skovsen, J. D. C. Lambert and P. R. Ogilby (2005) Subcellular, time-resolved studies of singlet oxygen in single cells. J. Am. Chem. Soc., 127, 14558-14559.
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 14558-14559
    • Snyder, J.W.1    Skovsen, E.2    Lambert, J.D.C.3    Ogilby, P.R.4
  • 18
    • 33750741490 scopus 로고    scopus 로고
    • UVB and UVA radiation-mediated damage to isolated and cellular DNA
    • Cadet, J., S. Courdavault, J.-L. Ravanat and T. Douki (2005) UVB and UVA radiation-mediated damage to isolated and cellular DNA. Pure Appl. Chem. 531, 5-23.
    • (2005) Pure Appl. Chem. , vol.531 , pp. 5-23
    • Cadet, J.1    Courdavault, S.2    Ravanat, J.-L.3    Douki, T.4
  • 19
    • 0011568510 scopus 로고
    • Chemistry of singlet oxygen. XVI. Long lifetime of singlet oxygen in carbon disulfide
    • Foote, C. S., Peterson, E. R., and Lee, K.-W. (1972) Chemistry of singlet oxygen. XVI. Long lifetime of singlet oxygen in carbon disulfide. J. Am. Chem. Soc. 94, 1032-1033.
    • (1972) J. Am. Chem. Soc. , vol.94 , pp. 1032-1033
    • Foote, C.S.1    Peterson, E.R.2    Lee, K.-W.3
  • 20
    • 0031005141 scopus 로고    scopus 로고
    • Determination of the quenching rate constants of singlet oxygen by derivatized nucleosides in nonaqueous solution
    • Prat, F., N. Houk and C. S. Foote (1997) Determination of the quenching rate constants of singlet oxygen by derivatized nucleosides in nonaqueous solution. J. Am. Chem. Soc. 119, 3951-3052.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 3951-13052
    • Prat, F.1    Houk, N.2    Foote, C.S.3
  • 21
    • 0023062822 scopus 로고
    • Laser flash photokinetic studies of rose bengal sensitized photodynamic interactions of nucleotides and DNA
    • Lee, P. C. C. and M. A. J. Rodgers (1987) Laser flash photokinetic studies of rose bengal sensitized photodynamic interactions of nucleotides and DNA. Photochem. Photobiol. 45, 79-86.
    • (1987) Photochem. Photobiol. , vol.45 , pp. 79-86
    • Lee, P.C.C.1    Rodgers, M.A.J.2
  • 22
    • 0028788870 scopus 로고
    • Reactivity toward singlet oxygen of a 7,8-dihydro-8-oxoguanosine ("8-hydroxyguanosine") formed by photooxidation of a guanosine derivative
    • Sheu, C., and C. S. Foote (1995) Reactivity toward singlet oxygen of a 7,8-dihydro-8-oxoguanosine ("8-hydroxyguanosine") formed by photooxidation of a guanosine derivative. J. Am. Chem. Soc. 117, 6439-6342.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 6439-16342
    • Sheu, C.1    Foote, C.S.2
  • 23
    • 0037123284 scopus 로고    scopus 로고
    • Low-temperature photosensitized oxidation of a guanosine derivative and formation of an imidazole ring-opened product
    • Sheu, C., P. Kang, S Khan, and C. S. Foote (2002) Low-temperature photosensitized oxidation of a guanosine derivative and formation of an imidazole ring-opened product. J. Am. Chem. Soc. 124, 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
  • 24
    • 0027134597 scopus 로고
    • Endoperoxide formation in a guanosine derivative
    • Sheu, C. and C. S. Foote (1993) Endoperoxide formation in a guanosine derivative. J. Am. Chem. Soc. 115, 10446-10447.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 10446-10447
    • Sheu, C.1    Foote, C.S.2
  • 25
    • 0036569575 scopus 로고    scopus 로고
    • Formation and transient intermediates in low temperature photosensitized oxidation of an 8-(13)C-guanosine
    • Kang, P. and C. S. Foote (2002) Formation and transient intermediates in low temperature photosensitized oxidation of an 8-(13)C-guanosine. J. Am. Chem. Soc. 124, 4865-4873.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 4865-4873
    • Kang, P.1    Foote, C.S.2
  • 26
    • 0037077633 scopus 로고    scopus 로고
    • 15N-labeled imidazole derivatives
    • 15N-labeled imidazole derivatives. J. Am. Chem. Soc. 124, 9629-9638.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 9629-9638
    • Kang, P.1    Foote, C.S.2
  • 27
    • 0001014503 scopus 로고
    • Phthalocyanine and naphthalocyanine photosensitized oxidation of 2′-deoxyguanosine: Distinct type I and type II products
    • Ravanat, J.-L., M. Berger, F. Benard, R. Langlois, R. Ouellet, J. E. van Lier and J. Cadet (1992) Phthalocyanine and naphthalocyanine photosensitized oxidation of 2′-deoxyguanosine: distinct type I and type II products. Photochem. Photobiol. 55, 809-814.
    • (1992) Photochem. Photobiol. , vol.55 , pp. 809-814
    • Ravanat, J.-L.1    Berger, M.2    Benard, F.3    Langlois, R.4    Ouellet, R.5    Van Lier, J.E.6    Cadet, J.7
  • 28
    • 0028927763 scopus 로고
    • Reaction of singlet oxygen with 2′-deoxyguanosine and DNA. Isolation and characterization of the main oxidation products
    • Ravanat, J.-L. and J. Cadet (1995) Reaction of singlet oxygen with 2′-deoxyguanosine and DNA. Isolation and characterization of the main oxidation products. Chem. Res. Toxicol. 8, 379-388.
    • (1995) Chem. Res. Toxicol. , vol.8 , pp. 379-388
    • Ravanat, J.-L.1    Cadet, J.2
  • 29
    • 0026700605 scopus 로고
    • Photooxidation of d(TpG) by naphthalocyanines and riboflavin. Isolation and characterization of dinucleoside monophosphates containing the 4R* and 4S* diastereoisomers of 4,8-dihydro-4-hydroxy-8-oxo-2′- deoxyguanosine
    • Buchko, G. W., J. Cadet, M. Berger and J.-L. Ravanat (1992) Photooxidation of d(TpG) by naphthalocyanines and riboflavin. Isolation and characterization of dinucleoside monophosphates containing the 4R* and 4S* diastereoisomers of 4,8-dihydro-4-hydroxy-8-oxo-2′- deoxyguanosine. Nucl. Acids Res. 20, 4847-4851.
    • (1992) Nucl. Acids Res. , vol.20 , pp. 4847-4851
    • Buchko, G.W.1    Cadet, J.2    Berger, M.3    Ravanat, J.-L.4
  • 30
    • 0035810395 scopus 로고    scopus 로고
    • Spiroiminodihydantoin is the major product of the 8-oxo-7,8- dihydroguanosine reaction with peroxynitrite in the presence of thiols and guanosine photooxidation by methylene blue
    • Niles, J. C., J. S. Wishnok and S. R. Tannenbaum (2001) Spiroiminodihydantoin is the major product of the 8-oxo-7,8-dihydroguanosine reaction with peroxynitrite in the presence of thiols and guanosine photooxidation by methylene blue. Org. Lett. 3, 963-966.
    • (2001) Org. Lett. , vol.3 , pp. 963-966
    • Niles, J.C.1    Wishnok, J.S.2    Tannenbaum, S.R.3
  • 31
    • 0034624588 scopus 로고    scopus 로고
    • Characterization of Spiroiminodihydantoin as a product of one-electron oxidation of 8-oxo-7,8-dihydroguanosine
    • Luo, W., J. G. Muller, E. M. Rachlin and C. J. Burrows, (2000) Characterization of Spiroiminodihydantoin as a product of one-electron oxidation of 8-oxo-7,8-dihydroguanosine, Org. Lett. 2, 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
  • 32
    • 0035817980 scopus 로고    scopus 로고
    • The pH-dependent role of superoxide in riboflavin-catalyzed photooxidation of 8-oxo-7,8-dihydroguanosine
    • Luo, W., J. G. Muller and C. J. Burrows, (2000) The pH-dependent role of superoxide in riboflavin-catalyzed photooxidation of 8-oxo-7,8-dihydroguanosine. Org. Lett. 3, 2801-2804.
    • (2000) Org. Lett. , vol.3 , pp. 2801-2804
    • Luo, W.1    Muller, J.G.2    Burrows, C.J.3
  • 33
    • 0034932109 scopus 로고    scopus 로고
    • Characterization of hydantoin products from one-electron of 8-oxo-7,8-dihydroguanosine in a nucleoside model
    • Luo, W., J. G. Muller, E. M. Rachlin and C. J. Burrows (2001). Characterization of hydantoin products from one-electron of 8-oxo-7,8- dihydroguanosine in a nucleoside model. Chem. Res. Toxicol. 14, 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
  • 34
    • 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., M. A. Arnold, M. Grune, W. M. Nau, U. Pischel and C. R. Saha-Möller (2002) 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, 537-540.
    • (2002) Org. Lett. , vol.4 , pp. 537-540
    • Adam, W.1    Arnold, M.A.2    Grune, M.3    Nau, W.M.4    Pischel, U.5    Saha-Möller, C.R.6
  • 35
    • 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, 607-617.
    • (2002) Biol. Chem. , vol.383 , pp. 607-617
    • Martinez, G.R.1    Medeiros, M.H.G.2    Ravanat, J.-L.3    Cadet, J.4    Di Mascio, P.5
  • 37
    • 11344258928 scopus 로고    scopus 로고
    • Characterization of 5-hydroxy-8-oxo-7,8-dihydroguanosine in the photosensitized oxidation of 8-oxo-7,8-dihydroguanosine and its rearrangement to spiroiminodihydantoin
    • McCallum, J. E. B., C. Y. Kuniyoshi and C. S. Foote (2004) Characterization of 5-hydroxy-8-oxo-7,8-dihydroguanosine in the photosensitized oxidation of 8-oxo-7,8-dihydroguanosine and its rearrangement to spiroiminodihydantoin. J. Am. Chem. Soc. 126, 16777-16782.
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 16777-16782
    • McCallum, J.E.B.1    Kuniyoshi, C.Y.2    Foote, C.S.3
  • 38
    • 17644395664 scopus 로고    scopus 로고
    • Spiroiminodihydantoin lesions derived from guanine oxidation: Structures, energetics, and functional implications
    • Lia, L., V. Shafirovich, R. Shapiro, N. E. Geacintov and S. Broyde (2005) Spiroiminodihydantoin lesions derived from guanine oxidation: Structures, energetics, and functional implications. Biochemistry 44, 6043-6051.
    • (2005) Biochemistry , vol.44 , pp. 6043-6051
    • Lia, L.1    Shafirovich, V.2    Shapiro, R.3    Geacintov, N.E.4    Broyde, S.5
  • 39
    • 26444571743 scopus 로고    scopus 로고
    • Structural and thermodynamic features of spiroiminodihydantoin damaged DNA duplexes
    • Lia, L., V. Shafirovich, R. Shapiro, N. E. Geacintov and S. Broyde (2005) Structural and thermodynamic features of spiroiminodihydantoin damaged DNA duplexes. Biochemistry 44, 13342-13353.
    • (2005) Biochemistry , vol.44 , pp. 13342-13353
    • Lia, L.1    Shafirovich, V.2    Shapiro, R.3    Geacintov, N.E.4    Broyde, S.5
  • 41
    • 0033938243 scopus 로고    scopus 로고
    • Singlet oxygen DNA damage products: Formation and measurement
    • Cadet, J., T. Douki, J.-P. Pouget and J.-L Ravanat (2000) Singlet oxygen DNA damage products: Formation and measurement. Methods Enzymol. 319, 143-153.
    • (2000) Methods Enzymol. , vol.319 , pp. 143-153
    • Cadet, J.1    Douki, T.2    Pouget, J.-P.3    Ravanat, J.-L.4
  • 42
    • 0344154463 scopus 로고    scopus 로고
    • Oxidative damage to DNA: Formation, measurement and biochemical features
    • Cadet, J., T. Douki, D. Gasparutto and J.-L. Ravanat (2003) Oxidative damage to DNA: Formation, measurement and biochemical features. Mutat. Res. 531, 5-23.
    • (2003) Mutat. Res. , vol.531 , pp. 5-23
    • Cadet, J.1    Douki, T.2    Gasparutto, D.3    Ravanat, J.-L.4
  • 45
    • 0026533905 scopus 로고
    • Substrate specificity of the Escherichia coli Fpg protein (formamidopyrimidine-DNA glycosylase): Excision of purine lesions in DNA produced by ionizing radiation or photosensitization
    • Boiteux, S., E. Gajewski, J. Laval and M. Dizdaroglu (1992) Substrate specificity of the Escherichia coli Fpg protein (formamidopyrimidine-DNA glycosylase): Excision of purine lesions in DNA produced by ionizing radiation or photosensitization. Biochemistry 31, 106-110.
    • (1992) Biochemistry , vol.31 , pp. 106-110
    • Boiteux, S.1    Gajewski, E.2    Laval, J.3    Dizdaroglu, M.4
  • 46
    • 0029124183 scopus 로고
    • Methylene blue-mediated photooxidation of 7,8-dihydro-8-oxo-2′- deoxyguanosine
    • Buchko, G. W., J. R. Wagner, J. Cadet, S. Raoul and M. Weinfeld (1995) Methylene blue-mediated photooxidation of 7,8-dihydro-8-oxo-2′- deoxyguanosine. Biochim. Biophys. Acta 1263, 17-24.
    • (1995) Biochim. Biophys. Acta , vol.1263 , pp. 17-24
    • Buchko, G.W.1    Wagner, J.R.2    Cadet, J.3    Raoul, S.4    Weinfeld, M.5
  • 47
    • 0029990148 scopus 로고    scopus 로고
    • Photosensitized reaction of 8-oxo-7,8-dihydro-2′-deoxyguanosine: Identification of 1-(2-deoxy-β-erythropentofuranosyl) cyanuric acid as the major singlet oxygen oxidation product
    • Raoul, S. and J. Cadet (1996) Photosensitized reaction of 8-oxo-7,8-dihydro-2′-deoxyguanosine: Identification of 1-(2-deoxy-β-erythropentofuranosyl) cyanuric acid as the major singlet oxygen oxidation product. J. Am. Chem. Soc. 118, 1892-1898.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 1892-1898
    • Raoul, S.1    Cadet, J.2
  • 49
    • 0028812702 scopus 로고
    • Photosensitized oxygenation of a 7,8-dihydro-8-oxoguanosine derivative. Formation of dioxetane and hydroperoxide intermediates
    • Sheu, C. and C. S. Foote (1995) Photosensitized oxygenation of a 7,8-dihydro-8-oxoguanosine derivative. Formation of dioxetane and hydroperoxide intermediates. J. Am. Chem. Soc. 117, 474-477.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 474-477
    • Sheu, C.1    Foote, C.S.2
  • 53
    • 0036917332 scopus 로고    scopus 로고
    • Characterization of the dehydro-guanidinohydantoin oxidation product of guanine in a dinucleotide
    • Chworos, A., C. Seguy, I. Dubey, G. Pratviel and B. Meunier (2002) Characterization of the dehydro-guanidinohydantoin oxidation product of guanine in a dinucleotide. Chem. Res. Toxicol. 15, 1643-1651.
    • (2002) Chem. Res. Toxicol. , vol.15 , pp. 1643-1651
    • Chworos, A.1    Seguy, C.2    Dubey, I.3    Pratviel, G.4    Meunier, B.5
  • 54
    • 0035929744 scopus 로고    scopus 로고
    • Characterization of an oxaluric acid derivative as a guanine oxidation product
    • Seguy, C., G. Pratviel and B. Meunier (2001) Characterization of an oxaluric acid derivative as a guanine oxidation product. Chem. Commun. 2001, 2116-2117.
    • (2001) Chem. Commun. , vol.2001 , pp. 2116-2117
    • Seguy, C.1    Pratviel, G.2    Meunier, B.3
  • 55
    • 33644815162 scopus 로고    scopus 로고
    • Identification of the α and β anomers of 1-(2-deoxy-D-erythro- pentofuranosyl)-oxaluric acid at the site of riboflavin-mediated photooxidation of guanine in 2′-deoxyguanosine and thymidylyl-(3′-5′)- 2′-deoxyguanosine
    • Buchko, G. W. and J. Cadet (2006) Identification of the α and β anomers of 1-(2-deoxy-D-erythro-pentofuranosyl)-oxaluric acid at the site of riboflavin-mediated photooxidation of guanine in 2′-deoxyguanosine and thymidylyl-(3′-5′)-2′-deoxyguanosine. Photochem. Photobiol. 82, 191-199.
    • (2006) Photochem. Photobiol. , vol.82 , pp. 191-199
    • Buchko, G.W.1    Cadet, J.2
  • 56
    • 33646080824 scopus 로고    scopus 로고
    • Mechanisms of formation, genotoxicity, and mutation of guanine oxidation products
    • Neeley, W. L. and J. M. Essigmann (2006) Mechanisms of formation, genotoxicity, and mutation of guanine oxidation products. Chem. Res. Toxicol. 19, 491-505.
    • (2006) Chem. Res. Toxicol. , vol.19 , pp. 491-505
    • Neeley, W.L.1    Essigmann, J.M.2
  • 58
    • 0033792418 scopus 로고    scopus 로고
    • High-performance liquid chromatography-tandem mass spectrometry measurement of radiation-induced base damage to isolated and cellular DNA
    • Frelon, S., T. Douki, J.-L. Ravanat, J.-P. Pouget, C. Tornabene and J. Cadet (2000) High-performance liquid chromatography-tandem mass spectrometry measurement of radiation-induced base damage to isolated and cellular DNA. Chem. Res. Toxicol. 13, 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
  • 59
    • 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., T. Douki, P. Duez, E. Gremaud, K. Herbert, T. Hofer, L. Lasserre, C. Saint-Pierre, A. Favier and J. Cadet (2002) 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, 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
  • 61
    • 14644433816 scopus 로고    scopus 로고
    • Ultraviolet radiation-mediated damage to cellular DNA
    • Cadet, J., E. Sage and T. Douki (2005) Ultraviolet radiation-mediated damage to cellular DNA. Mutat. Res. 571, 3-17.
    • (2005) Mutat. Res. , vol.571 , pp. 3-17
    • Cadet, J.1    Sage, E.2    Douki, T.3
  • 62
    • 0027140196 scopus 로고
    • Effect of ascorbate and 5-aminolevulinic acid on light-induced 8-hydroxydeoxyguanosine formation in V79 Chinese hamster cells
    • Fisher-Nilsen, A., S. Loft and K. G. Jensen (1993) Effect of ascorbate and 5-aminolevulinic acid on light-induced 8-hydroxydeoxyguanosine formation in V79 Chinese hamster cells. Carcinogenesis 14, 2431-2433.
    • (1993) Carcinogenesis , vol.14 , pp. 2431-2433
    • Fisher-Nilsen, A.1    Loft, S.2    Jensen, K.G.3
  • 63
    • 0030198720 scopus 로고
    • 8-Oxodeoxyguanosine formation in the DNA of cultured cells after exposure alone or with UVB or UVA irradiation
    • Rosen, J. E., A. K. Prahalad and G. M. Williams (1096) 8-Oxodeoxyguanosine formation in the DNA of cultured cells after exposure alone or with UVB or UVA irradiation. Photochem. Photobiol. 64, 117-122.
    • (1096) Photochem. Photobiol. , vol.64 , pp. 117-122
    • Rosen, J.E.1    Prahalad, A.K.2    Williams, G.M.3
  • 64
    • 0031058073 scopus 로고    scopus 로고
    • Induction of 8-oxo-7,8-dihydro-2′-deoxyguanosine by ultraviolet radiation in calf thymus DNA and HeLa cells
    • Zhang, X., B. S. Rosenstein, Y. Wang, M. Lebwohl, D. L. Mitchell and H. Wei (1997) Induction of 8-oxo-7,8-dihydro-2′-deoxyguanosine by ultraviolet radiation in calf thymus DNA and HeLa cells. Photochem. Photobiol. 65, 119-124.
    • (1997) Photochem. Photobiol. , vol.65 , pp. 119-124
    • Zhang, X.1    Rosenstein, B.S.2    Wang, Y.3    Lebwohl, M.4    Mitchell, D.L.5    Wei, H.6
  • 65
    • 0031409635 scopus 로고    scopus 로고
    • Induction of oxidative DNA base damage in human skin cells by UV and near visible radiation
    • Kvam, E. and R. M. Tyrell (1997) Induction of oxidative DNA base damage in human skin cells by UV and near visible radiation. Carcinogenesis 18, 2379-2384.
    • (1997) Carcinogenesis , vol.18 , pp. 2379-2384
    • Kvam, E.1    Tyrell, R.M.2
  • 67
    • 0035007619 scopus 로고    scopus 로고
    • Photodynamic DNA damage mediated by δ-aminolevulinic acid-induced porphyrin
    • Duez, P., M. Hanocq and J. Dubois (2001) Photodynamic DNA damage mediated by δ-aminolevulinic acid-induced porphyrin. Carcinogenesis 22, 771-778.
    • (2001) Carcinogenesis , vol.22 , pp. 771-778
    • Duez, P.1    Hanocq, M.2    Dubois, J.3
  • 68
    • 5644238093 scopus 로고    scopus 로고
    • Larger yield of cyclobutane dimers than 8-oxo-7,8-dihydroguanine in the DNA of UVA-irradiated human skin cells
    • Courdavault, S., C. Baudoin, M. Charveron, A. Favier, J. Cadet and T. Douki (2004) Larger yield of cyclobutane dimers than 8-oxo-7,8-dihydroguanine in the DNA of UVA-irradiated human skin cells. Mutat. Res. 556, 135-142.
    • (2004) Mutat. Res. , vol.556 , pp. 135-142
    • Courdavault, S.1    Baudoin, C.2    Charveron, M.3    Favier, A.4    Cadet, J.5    Douki, T.6
  • 69
    • 3042519214 scopus 로고    scopus 로고
    • G-to-T tranversions and small tandem base deletions are the hallmark of mutations by ultraviolet a radiation in mammalian cells
    • Besaratinia, A., T. W. Synold, B. Xi and G. P. Pfeifer (2004) G-to-T tranversions and small tandem base deletions are the hallmark of mutations by ultraviolet A radiation in mammalian cells. Biochemistry 43, 8169-8177.
    • (2004) Biochemistry , vol.43 , pp. 8169-8177
    • Besaratinia, A.1    Synold, T.W.2    Xi, B.3    Pfeifer, G.P.4
  • 70
    • 22544452379 scopus 로고    scopus 로고
    • DNA lesions induced by UV A1 and B radiation in human cells: Comparative analyses in the overall genome and in the p53 tumor suppressor gene
    • Besaratinia, A., T. W. Synold, H.-H. Chen, C. Chang C, B. Xi, A. D. Riggs and G. P. Pfeifer (2005) DNA lesions induced by UV A1 and B radiation in human cells: Comparative analyses in the overall genome and in the p53 tumor suppressor gene. Proc. Natl. Acad. Sci. USA 102, 10058-10063.
    • (2005) Proc. Natl. Acad. Sci. USA , vol.102 , pp. 10058-10063
    • Besaratinia, A.1    Synold, T.W.2    Chen, H.-H.3    Chang, C.4    Xi, B.5    Riggs, A.D.6    Pfeifer, G.P.7
  • 71
    • 0033914527 scopus 로고    scopus 로고
    • DNA damage induced in cells by γ and UVA radiation as measured by HPLC/GC-MS and HPLC-EC and comet assay
    • Pouget, J.-P., T. Douki, M.-J. Richard and J. Cadet (2000) DNA damage induced in cells by γ and UVA radiation as measured by HPLC/GC-MS and HPLC-EC and comet assay. Chem. Res. Toxicol. 13, 541-549.
    • (2000) Chem. Res. Toxicol. , vol.13 , pp. 541-549
    • Pouget, J.-P.1    Douki, T.2    Richard, M.-J.3    Cadet, J.4
  • 72
    • 0031426132 scopus 로고    scopus 로고
    • Wavelength dependence of oxidative DNA damage induced by UV and visible light
    • Kielbalssa, C., L. Roza and B. Epe (1997) Wavelength dependence of oxidative DNA damage induced by UV and visible light. Carcinogenesis 18, 811-817.
    • (1997) Carcinogenesis , vol.18 , pp. 811-817
    • Kielbalssa, C.1    Roza, L.2    Epe, B.3
  • 73
    • 33750741646 scopus 로고    scopus 로고
    • Pfaum M., C. Kielbassa, M. Garmyn and B. Epe (1998) Oxidative DNA damage induced by visible light in mammalian cells: Extent
    • Pfaum M., C. Kielbassa, M. Garmyn and B. Epe (1998) Oxidative DNA damage induced by visible light in mammalian cells: Extent,


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