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Volumn 50, Issue 8, 2012, Pages 2822-2830

Structural influence of isothiocyanates on expression of cytochrome P450, phase II enzymes, and activation of Nrf2 in primary rat hepatocytes

Author keywords

Cytochrome 450; Isothiocyanate; Nrf2; Oxidative stress; Phase II

Indexed keywords

ALLYL ISOTHIOCYANATE; ANTIOXIDANT; BENZYL ISOTHIOCYANATE; BENZYLOXYQUINOLINE DEBENZYLASE; CATALASE; CYTOCHROME P450; CYTOCHROME P450 1A1; CYTOCHROME P450 1A2; CYTOCHROME P450 3A2; ETHOXYRESORUFIN DEETHYLASE; GLUTATHIONE TRANSFERASE; HEME OXYGENASE 1; IBCRIN ISOTHIOCYANATE; ISOTHIOCYANIC ACID DERIVATIVE; NAPIN ISOTHIOCYANATE; PHENETHYL ISOTHIOCYANATE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE (PHOSPHATE) DEHYDROGENASE (QUINONE); RHAPHASATIN ISOTHIOCYANATE; SULFORAPHANE; TRANSCRIPTION FACTOR NRF2; UNCLASSIFIED DRUG;

EID: 84862689618     PISSN: 02786915     EISSN: 18736351     Source Type: Journal    
DOI: 10.1016/j.fct.2012.05.044     Document Type: Article
Times cited : (51)

References (54)
  • 2
    • 0018170362 scopus 로고
    • A simple and sensitive assay of-7-ethoxycoumarin deethylation
    • Aitio A. A simple and sensitive assay of-7-ethoxycoumarin deethylation. Anal. Biochem. 1978, 85:488-491.
    • (1978) Anal. Biochem. , vol.85 , pp. 488-491
    • Aitio, A.1
  • 3
    • 0029680494 scopus 로고    scopus 로고
    • Microsomal oxidation of N,N-diethylformamide and its effect on P450-dependent monooxygenases in rat liver
    • Amato G., Longo V., Mazzaccaro A., Gervasi P.G. Microsomal oxidation of N,N-diethylformamide and its effect on P450-dependent monooxygenases in rat liver. Chem. Res. Toxicol. 1996, 9:882-890.
    • (1996) Chem. Res. Toxicol. , vol.9 , pp. 882-890
    • Amato, G.1    Longo, V.2    Mazzaccaro, A.3    Gervasi, P.G.4
  • 4
    • 0037569694 scopus 로고    scopus 로고
    • Curcumin activates the heme oxygenase-1 gene via regulation of Nrf2 and the antioxidant-responsive element
    • Balogun E., Hoque M., Gong P., Killeen E., Green C.J., Foresti R., Alam J., Motterlini R. Curcumin activates the heme oxygenase-1 gene via regulation of Nrf2 and the antioxidant-responsive element. Biochem. J. 2003, 371:887-895.
    • (2003) Biochem. J. , vol.371 , pp. 887-895
    • Balogun, E.1    Hoque, M.2    Gong, P.3    Killeen, E.4    Green, C.J.5    Foresti, R.6    Alam, J.7    Motterlini, R.8
  • 6
    • 0019142866 scopus 로고
    • Increase of NAD(P)H:quinone reductase by dietary antioxidants: possible role in protection against carcinogenesis and toxicity
    • Bensen A.M., Hunkeler M.S., Talalay P. Increase of NAD(P)H:quinone reductase by dietary antioxidants: possible role in protection against carcinogenesis and toxicity. Proc. Natl. Acad. Sci. USA 1980, 77:5216-5220.
    • (1980) Proc. Natl. Acad. Sci. USA , vol.77 , pp. 5216-5220
    • Bensen, A.M.1    Hunkeler, M.S.2    Talalay, P.3
  • 7
    • 0016333916 scopus 로고
    • Ethoxyresorufin: direct fluorimetric assay of a microsomal O-dealkylation which is preferentially inducible by 3-methylcholanthrene
    • Burke M.D., Mayer R.T. Ethoxyresorufin: direct fluorimetric assay of a microsomal O-dealkylation which is preferentially inducible by 3-methylcholanthrene. Drug Metab. Dispos. 1974, 2:583-588.
    • (1974) Drug Metab. Dispos. , vol.2 , pp. 583-588
    • Burke, M.D.1    Mayer, R.T.2
  • 8
    • 0036297295 scopus 로고    scopus 로고
    • Chemical induction of cellular antioxidants affords marked protection against oxidative injury in vascular smooth muscle cells
    • Cao Z., Li Y. Chemical induction of cellular antioxidants affords marked protection against oxidative injury in vascular smooth muscle cells. Biochem. Biophys. Res. Commun. 2002, 292:50-57.
    • (2002) Biochem. Biophys. Res. Commun. , vol.292 , pp. 50-57
    • Cao, Z.1    Li, Y.2
  • 9
    • 77449106593 scopus 로고    scopus 로고
    • Molecular targets of dietary phenylethyl isothiocyanate and sulforaphane for cancer chemoprevention
    • Cheung K.L., Kong A. Molecular targets of dietary phenylethyl isothiocyanate and sulforaphane for cancer chemoprevention. AAPS J. 2010, 12:87-97.
    • (2010) AAPS J. , vol.12 , pp. 87-97
    • Cheung, K.L.1    Kong, A.2
  • 10
    • 0029801147 scopus 로고    scopus 로고
    • Inhibition of rat liver cytochrome P450 isoenzymes by isothiocyanates and their conjugates: a structure-activity relationship study
    • Conaway C.C., Jiao D., Chung F.L. Inhibition of rat liver cytochrome P450 isoenzymes by isothiocyanates and their conjugates: a structure-activity relationship study. Carcinogenesis 1996, 17:2423-2427.
    • (1996) Carcinogenesis , vol.17 , pp. 2423-2427
    • Conaway, C.C.1    Jiao, D.2    Chung, F.L.3
  • 11
    • 0035987188 scopus 로고    scopus 로고
    • Isothiocyanates as cancer chemopreventive agents: their biological activities and metabolism in rodents and humans
    • Conaway C.C., Yang Y.M., Chung F.L. Isothiocyanates as cancer chemopreventive agents: their biological activities and metabolism in rodents and humans. Curr. Drug Metab. 2002, 3:233-255.
    • (2002) Curr. Drug Metab. , vol.3 , pp. 233-255
    • Conaway, C.C.1    Yang, Y.M.2    Chung, F.L.3
  • 12
    • 0023738916 scopus 로고
    • A quick and simple method for the quantitation of lactate dehydrogenase release in measurements of cellular cytotoxicity and tumor necrosis factor (TNF) activity
    • Deker T., Lohmann-Matthes M. A quick and simple method for the quantitation of lactate dehydrogenase release in measurements of cellular cytotoxicity and tumor necrosis factor (TNF) activity. J. Immunol. Methods 1988, 15:61-69.
    • (1988) J. Immunol. Methods , vol.15 , pp. 61-69
    • Deker, T.1    Lohmann-Matthes, M.2
  • 13
    • 0038768712 scopus 로고    scopus 로고
    • Activation of the aryl hydrocarbon receptor by structurally diverse exogenous and endogenous chemicals
    • Denison M.S., Nagy S.R. Activation of the aryl hydrocarbon receptor by structurally diverse exogenous and endogenous chemicals. Annu. Rev. Pharmacol. Toxicol. 2003, 43:309-334.
    • (2003) Annu. Rev. Pharmacol. Toxicol. , vol.43 , pp. 309-334
    • Denison, M.S.1    Nagy, S.R.2
  • 15
    • 0037015035 scopus 로고    scopus 로고
    • Direct evidence that sulfhydryl groups of Keap1 are the sensors regulating induction of phase 2 enzymes that protect against carcinogens and oxidants
    • Dinkova-Kostova A.T., Holtzclaw W.D., Cole R.N., Itoh K., Wakabayashi N., Katoh Y., Yamamonto M., Talalay P. Direct evidence that sulfhydryl groups of Keap1 are the sensors regulating induction of phase 2 enzymes that protect against carcinogens and oxidants. Proc. Natl. Acad. Sci. USA 2002, 99:11908-11913.
    • (2002) Proc. Natl. Acad. Sci. USA , vol.99 , pp. 11908-11913
    • Dinkova-Kostova, A.T.1    Holtzclaw, W.D.2    Cole, R.N.3    Itoh, K.4    Wakabayashi, N.5    Katoh, Y.6    Yamamonto, M.7    Talalay, P.8
  • 16
    • 0030931522 scopus 로고    scopus 로고
    • Broccoli sprouts: an exceptionally rich source of inducers of enzymes that protect against chemical carcinogens
    • Fahey J.W., Zhang Y., Talalay P. Broccoli sprouts: an exceptionally rich source of inducers of enzymes that protect against chemical carcinogens. Proc. Natl. Acad. Sci. USA 1997, 94:10367-10372.
    • (1997) Proc. Natl. Acad. Sci. USA , vol.94 , pp. 10367-10372
    • Fahey, J.W.1    Zhang, Y.2    Talalay, P.3
  • 17
    • 84864073242 scopus 로고
    • Springer-Verlang, E-publishing Inc., Berlin
    • Funae Y., Imaoka S. 1993, 221-223. Springer-Verlang, E-publishing Inc., Berlin.
    • (1993) , pp. 221-223
    • Funae, Y.1    Imaoka, S.2
  • 18
    • 0035204635 scopus 로고    scopus 로고
    • Effects of benzyl isothiocyanatte on rat and human cytochrome P450: identification of metabolites formed by P450 2B1
    • Goosen T.C., Mills D.E., Hollenberg P.F. Effects of benzyl isothiocyanatte on rat and human cytochrome P450: identification of metabolites formed by P450 2B1. J. Pharmacol. Exp. Ther. 2001, 296:198-206.
    • (2001) J. Pharmacol. Exp. Ther. , vol.296 , pp. 198-206
    • Goosen, T.C.1    Mills, D.E.2    Hollenberg, P.F.3
  • 19
    • 77955079408 scopus 로고    scopus 로고
    • Sulforaphane- and phenethyl isothiocyanate-induced inhibition of aflotoxin B1-mediated genotoxicity in human hepatocytes: role of GSTM1 genotype and CYP3A4 gene expression
    • Gross-Steinmeyer K., Stapleton P.L., Tracy J.H., Bammler T.K., Strom S.C., Eaton D.L. Sulforaphane- and phenethyl isothiocyanate-induced inhibition of aflotoxin B1-mediated genotoxicity in human hepatocytes: role of GSTM1 genotype and CYP3A4 gene expression. Toxicol. Sci. 2010, 116:422-432.
    • (2010) Toxicol. Sci. , vol.116 , pp. 422-432
    • Gross-Steinmeyer, K.1    Stapleton, P.L.2    Tracy, J.H.3    Bammler, T.K.4    Strom, S.C.5    Eaton, D.L.6
  • 20
    • 0016275313 scopus 로고
    • Glutathione S-transferases. The first enzymatic step in mercapturic acid formation
    • Habig W.H., Pabst M.J., Jakoby W.B. Glutathione S-transferases. The first enzymatic step in mercapturic acid formation. J. Biol. Chem. 1974, 249:7130-7139.
    • (1974) J. Biol. Chem. , vol.249 , pp. 7130-7139
    • Habig, W.H.1    Pabst, M.J.2    Jakoby, W.B.3
  • 21
    • 53249140296 scopus 로고    scopus 로고
    • Up-regulation of the CYP1 family in rat and human liver by the aliphatic isothiocyanates erucin and sulforaphane
    • Hanlon N., Codham N., Sauer M.J., Ioannides C. Up-regulation of the CYP1 family in rat and human liver by the aliphatic isothiocyanates erucin and sulforaphane. Toxicology 2008, 252:92-98.
    • (2008) Toxicology , vol.252 , pp. 92-98
    • Hanlon, N.1    Codham, N.2    Sauer, M.J.3    Ioannides, C.4
  • 22
    • 68149167105 scopus 로고    scopus 로고
    • The aliphatic isothiocyanates erucin and sulforaphane do not effectively up-regulate NAD(P)H:quinone oxidoreductese (NQO1) in human liver compared to rat
    • Hanlon N., Poynton C.L., Codham N., Sauer M.J., Ioannides C. The aliphatic isothiocyanates erucin and sulforaphane do not effectively up-regulate NAD(P)H:quinone oxidoreductese (NQO1) in human liver compared to rat. Mol. Nutr. Food Res. 2009, 53:836-844.
    • (2009) Mol. Nutr. Food Res. , vol.53 , pp. 836-844
    • Hanlon, N.1    Poynton, C.L.2    Codham, N.3    Sauer, M.J.4    Ioannides, C.5
  • 23
    • 43149099706 scopus 로고    scopus 로고
    • The cancer chemopreventive actions of phytochemicals derived from glucosinolates
    • Hayes J.D., Kelleher M.O., Eggleston I.M. The cancer chemopreventive actions of phytochemicals derived from glucosinolates. Eur. J. Nutr. 2008, 47:73-88.
    • (2008) Eur. J. Nutr. , vol.47 , pp. 73-88
    • Hayes, J.D.1    Kelleher, M.O.2    Eggleston, I.M.3
  • 24
    • 0032953192 scopus 로고    scopus 로고
    • Keap1 represses nuclear activation of antioxidant responsive elements by Nrf2 through binding to the amino-terminal Neh2 domain
    • Itoh K., Wakabayashi N., Katoh Y., Ishii T. Keap1 represses nuclear activation of antioxidant responsive elements by Nrf2 through binding to the amino-terminal Neh2 domain. Genes Dev. 1999, 13:76-86.
    • (1999) Genes Dev. , vol.13 , pp. 76-86
    • Itoh, K.1    Wakabayashi, N.2    Katoh, Y.3    Ishii, T.4
  • 25
    • 0013785031 scopus 로고
    • The preparation of microsomes. naunyn-schmiedebergs
    • Jagow R., Kampffmeyer H., Kinese M. The preparation of microsomes. naunyn-schmiedebergs. Arch. Pharm. 1965, 251:73-87.
    • (1965) Arch. Pharm. , vol.251 , pp. 73-87
    • Jagow, R.1    Kampffmeyer, H.2    Kinese, M.3
  • 26
    • 20444438012 scopus 로고    scopus 로고
    • Differential expression and stability of endogenous nuclear factor E2-related factor 2 (Nrf2) by natural chemopreventive compounds in HepG2 human hepatoma cells
    • Jeong W.S., Keum Y.S., Chen Chi., Jain M.R., Shen G., Kim J.H., Li W., Kong Ah-Ng T. Differential expression and stability of endogenous nuclear factor E2-related factor 2 (Nrf2) by natural chemopreventive compounds in HepG2 human hepatoma cells. J. Biochem. Mol. Biol. 2005, 38:167-176.
    • (2005) J. Biochem. Mol. Biol. , vol.38 , pp. 167-176
    • Jeong, W.S.1    Keum, Y.S.2    Chen, C.3    Jain, M.R.4    Shen, G.5    Kim, J.H.6    Li, W.7    Kong Ah-Ng, T.8
  • 27
    • 34247606510 scopus 로고    scopus 로고
    • Molecular basis for chemoprevention by sulforaphane: a comprehensive review
    • Juge N., Mithen R.F., Traka M. Molecular basis for chemoprevention by sulforaphane: a comprehensive review. Cell. Mol. Life Sci. 2007, 64:1105-1127.
    • (2007) Cell. Mol. Life Sci. , vol.64 , pp. 1105-1127
    • Juge, N.1    Mithen, R.F.2    Traka, M.3
  • 28
    • 40949104732 scopus 로고    scopus 로고
    • 3-Morpholinopropyl isothiocynate is a novel synthetic isothiocyanate that strongly induces the antioxidant response element-dependent Nrf2-mediated detoxifying/antioxidant enzymes in vitro and in vivo
    • Keum Y.S., Chang P.P., Kwon K.H., Yuan X., Li W., Hu L., Kong A. 3-Morpholinopropyl isothiocynate is a novel synthetic isothiocyanate that strongly induces the antioxidant response element-dependent Nrf2-mediated detoxifying/antioxidant enzymes in vitro and in vivo. Carcinogenesis 2008, 29:594-599.
    • (2008) Carcinogenesis , vol.29 , pp. 594-599
    • Keum, Y.S.1    Chang, P.P.2    Kwon, K.H.3    Yuan, X.4    Li, W.5    Hu, L.6    Kong, A.7
  • 29
    • 0014949207 scopus 로고
    • Cleavage of structural proteins during the assembly of the head of bacteriophage T4
    • Laemmli U.K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 1970, 227:680-685.
    • (1970) Nature , vol.227 , pp. 680-685
    • Laemmli, U.K.1
  • 31
    • 0034691291 scopus 로고    scopus 로고
    • Hydrolysis of glucosinolates using nylon-immobilized myrosinase to produce pure bioactive molecules
    • Leoni O., Iori R., Palmieri S. Hydrolysis of glucosinolates using nylon-immobilized myrosinase to produce pure bioactive molecules. Biotechnol. Bioeng. 2000, 68:660-664.
    • (2000) Biotechnol. Bioeng. , vol.68 , pp. 660-664
    • Leoni, O.1    Iori, R.2    Palmieri, S.3
  • 33
    • 0030852501 scopus 로고    scopus 로고
    • Inibithion of cytochromes P-450 and induction of glutathione S-transferase by sulforaphane in primary human and rat hepatocytes
    • Mahèo K., Morel F., Langouët S., Kramer H., Le Ferrec E., Ketterer B., Guillouzo A. Inibithion of cytochromes P-450 and induction of glutathione S-transferase by sulforaphane in primary human and rat hepatocytes. Cancer. Res. 1997, 57:3649-3652.
    • (1997) Cancer. Res. , vol.57 , pp. 3649-3652
    • Mahèo, K.1    Morel, F.2    Langouët, S.3    Kramer, H.4    Le Ferrec, E.5    Ketterer, B.6    Guillouzo, A.7
  • 34
    • 0030912435 scopus 로고    scopus 로고
    • Expression and inducibility of cytochrome P4503A9 (CYP3A9) and other members of the CYP3A subfamily in tat liver
    • Mahnke A., Strotkamp D., Roos P.H., Hanstein W.G., Chabot G.G., Nef P. Expression and inducibility of cytochrome P4503A9 (CYP3A9) and other members of the CYP3A subfamily in tat liver. Arch. Biochem. Biophys. 1997, 337:62-68.
    • (1997) Arch. Biochem. Biophys. , vol.337 , pp. 62-68
    • Mahnke, A.1    Strotkamp, D.2    Roos, P.H.3    Hanstein, W.G.4    Chabot, G.G.5    Nef, P.6
  • 35
    • 77249089780 scopus 로고    scopus 로고
    • Electrophiles in foods: the current status of isothiocyanates and their chemical biology
    • Nakamura Y., Miyoshi N. Electrophiles in foods: the current status of isothiocyanates and their chemical biology. Biosci. Biotechnol. Biochem. 2010, 74:242-255.
    • (2010) Biosci. Biotechnol. Biochem. , vol.74 , pp. 242-255
    • Nakamura, Y.1    Miyoshi, N.2
  • 37
    • 0034815141 scopus 로고    scopus 로고
    • Reactive oxygen species-related induction of multidrug resistance-associated protein 2 expression in primary hepatocytes exposed to sulforaphane
    • Payen L., Courtois A., Loewert K., Guillouzo A., Fardel O. Reactive oxygen species-related induction of multidrug resistance-associated protein 2 expression in primary hepatocytes exposed to sulforaphane. Biochem. Biophys. Res. Comm. 2001, 282:257-263.
    • (2001) Biochem. Biophys. Res. Comm. , vol.282 , pp. 257-263
    • Payen, L.1    Courtois, A.2    Loewert, K.3    Guillouzo, A.4    Fardel, O.5
  • 38
    • 0028127980 scopus 로고
    • Design and synthesis of bifunctional isothiocyanate analogs of sulforaphane. Correlation between structure and potency as inducers of anticancer detoxication enzymes
    • Postner G.H., Cho C., Green J.V., Zhang Y., Talalay P. Design and synthesis of bifunctional isothiocyanate analogs of sulforaphane. Correlation between structure and potency as inducers of anticancer detoxication enzymes. J. Med. Chem. 1994, 37:170-176.
    • (1994) J. Med. Chem. , vol.37 , pp. 170-176
    • Postner, G.H.1    Cho, C.2    Green, J.V.3    Zhang, Y.4    Talalay, P.5
  • 39
    • 43349098881 scopus 로고    scopus 로고
    • Structural influence of isothiocyanates on the antioxidant response element (ARE)-mediated oxygenase (HO-1) expression
    • Prawn A., Keum Y., Khor T.O., Yu S., Nair S., Li W., Hu L., Kong A. Structural influence of isothiocyanates on the antioxidant response element (ARE)-mediated oxygenase (HO-1) expression. Pharmac. Res. 2008, 25:836-844.
    • (2008) Pharmac. Res. , vol.25 , pp. 836-844
    • Prawn, A.1    Keum, Y.2    Khor, T.O.3    Yu, S.4    Nair, S.5    Li, W.6    Hu, L.7    Kong, A.8
  • 40
    • 77957876664 scopus 로고    scopus 로고
    • Intact Glucosinolates modulate hepatic cytochrome P450 and phase II conjugation activities and may contribute directly to the chemopreventive activity of cruciferous vegetables
    • Razis A.F.A., Bagatta M., De Nicola G.R., Iori R., Ioannides C. Intact Glucosinolates modulate hepatic cytochrome P450 and phase II conjugation activities and may contribute directly to the chemopreventive activity of cruciferous vegetables. Toxicology 2010, 277:74-85.
    • (2010) Toxicology , vol.277 , pp. 74-85
    • Razis, A.F.A.1    Bagatta, M.2    De Nicola, G.R.3    Iori, R.4    Ioannides, C.5
  • 41
    • 0027325487 scopus 로고
    • Mechanism of inhibition of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone bioactivation in mouse by dietary phenyl ethyl isothiocyanate
    • Smith T.J., Guo Z., Li C., Ning S.M., Thomas P.E., Yang C.S. Mechanism of inhibition of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone bioactivation in mouse by dietary phenyl ethyl isothiocyanate. Cancer Res. 1993, 53:3276-3282.
    • (1993) Cancer Res. , vol.53 , pp. 3276-3282
    • Smith, T.J.1    Guo, Z.2    Li, C.3    Ning, S.M.4    Thomas, P.E.5    Yang, C.S.6
  • 42
  • 43
    • 77954362516 scopus 로고    scopus 로고
    • Sandwich-cultured hepatocytes: an in vitro model to evaluate hepatobiliary transporter-based drug interactions and hepatotoxicity
    • Swift B., Pfeifer N.D., Brower K.L.R. Sandwich-cultured hepatocytes: an in vitro model to evaluate hepatobiliary transporter-based drug interactions and hepatotoxicity. Drug Metab. Rev. 2010, 42:446-471.
    • (2010) Drug Metab. Rev. , vol.42 , pp. 446-471
    • Swift, B.1    Pfeifer, N.D.2    Brower, K.L.R.3
  • 44
    • 0029053409 scopus 로고
    • Dietary glucosinolates as blocking agents against carcinogenesis: glucosinolate breakdown products assessed by induction of quinone reductase activity in murine hepa1c1c7 cells
    • Tawfiq N., Heaney R.K., Plumb J.A., Fenwick G.R., Musk S.R., Williamson G. Dietary glucosinolates as blocking agents against carcinogenesis: glucosinolate breakdown products assessed by induction of quinone reductase activity in murine hepa1c1c7 cells. Carcinogenesis 1995, 16:1191-1194.
    • (1995) Carcinogenesis , vol.16 , pp. 1191-1194
    • Tawfiq, N.1    Heaney, R.K.2    Plumb, J.A.3    Fenwick, G.R.4    Musk, S.R.5    Williamson, G.6
  • 45
    • 0009482260 scopus 로고
    • Electrophoretic transfer of proteins from polyacrylamide gel to nitrocellulose sheets: procedure and some applications
    • Towbin H.T., Staehelin P., Gordon J. Electrophoretic transfer of proteins from polyacrylamide gel to nitrocellulose sheets: procedure and some applications. Proc. Natl. Acad. Sci. USA 1979, 76:4350-4354.
    • (1979) Proc. Natl. Acad. Sci. USA , vol.76 , pp. 4350-4354
    • Towbin, H.T.1    Staehelin, P.2    Gordon, J.3
  • 46
    • 33746933154 scopus 로고    scopus 로고
    • Association between consumption of cruciferous vegetables and condiments and excretion in urine of isothiocyanate mercapturico acids
    • Vermeulen M., van der Berg R., Freidig A.P., van Bladeren P.J., Vaes W.H.J. Association between consumption of cruciferous vegetables and condiments and excretion in urine of isothiocyanate mercapturico acids. J. Agric. Food. Chem. 2006, 54:5350-5358.
    • (2006) J. Agric. Food. Chem. , vol.54 , pp. 5350-5358
    • Vermeulen, M.1    van der Berg, R.2    Freidig, A.P.3    van Bladeren, P.J.4    Vaes, W.H.J.5
  • 47
    • 65549122133 scopus 로고    scopus 로고
    • Potency of isothiocyanates to induce luciferase reporter gene expression via the electrophile-responsive element from murine glutathione S-transferase Ya
    • Vermeulen M., Boerboom A.M., Blankvoort B.M., Aarts J.M., Rietjens I.M., van Bladeren P.J., Vaes W.H. Potency of isothiocyanates to induce luciferase reporter gene expression via the electrophile-responsive element from murine glutathione S-transferase Ya. Toxicol. in Vitro 2009, 23:617-621.
    • (2009) Toxicol. in Vitro , vol.23 , pp. 617-621
    • Vermeulen, M.1    Boerboom, A.M.2    Blankvoort, B.M.3    Aarts, J.M.4    Rietjens, I.M.5    van Bladeren, P.J.6    Vaes, W.H.7
  • 48
    • 0001923588 scopus 로고
    • Isolation and identification for trans-4-(methylthio)-3-butenyl glucosinolate from radish roots (Raphanus sativus L.)
    • Visentin M., Tava A., Iori R., Palmieri S. Isolation and identification for trans-4-(methylthio)-3-butenyl glucosinolate from radish roots (Raphanus sativus L.). J. Agric. Food Chem. 1992, 40:1687-1691.
    • (1992) J. Agric. Food Chem. , vol.40 , pp. 1687-1691
    • Visentin, M.1    Tava, A.2    Iori, R.3    Palmieri, S.4
  • 49
    • 66749170767 scopus 로고    scopus 로고
    • Are isothiocyanates potential anti-cancer drugs?
    • Xiang Wu., Qiah-hua Zhou., Ke Xu. Are isothiocyanates potential anti-cancer drugs?. Acta Pharmacol. Sin. 2009, 30:501-512.
    • (2009) Acta Pharmacol. Sin. , vol.30 , pp. 501-512
    • Xiang, W.1    Qiah-hua, Z.2    Ke, X.3
  • 50
    • 0028324459 scopus 로고
    • Cytochrome P450 enzymes as targets for chemoprevention against chemical carcinogenesis and toxicity. opportunities and limitations
    • Yang C.S., Smith T.J., Hong J.Y. Cytochrome P450 enzymes as targets for chemoprevention against chemical carcinogenesis and toxicity. opportunities and limitations. Cancer Res. 1994, 54:1982s-1986s.
    • (1994) Cancer Res. , vol.54
    • Yang, C.S.1    Smith, T.J.2    Hong, J.Y.3
  • 51
    • 0035681887 scopus 로고    scopus 로고
    • Total intracellular accumulation levels of dietary isothiocyanates determine their activity in elevation of cellular glutathione and induction of Phase 2 detoxification enzymes
    • Ye L., Zhang Y. Total intracellular accumulation levels of dietary isothiocyanates determine their activity in elevation of cellular glutathione and induction of Phase 2 detoxification enzymes. Carcinogenesis 2001, 22:1987-1992.
    • (2001) Carcinogenesis , vol.22 , pp. 1987-1992
    • Ye, L.1    Zhang, Y.2
  • 52
    • 0028326168 scopus 로고
    • Anticarcinogenic activities of organic isothiocyanates: chemistry and mechanisms
    • Zhang Y., Talalay P. Anticarcinogenic activities of organic isothiocyanates: chemistry and mechanisms. Cancer Res. 1994, 54:1976-1981.
    • (1994) Cancer Res. , vol.54 , pp. 1976-1981
    • Zhang, Y.1    Talalay, P.2
  • 53
    • 74349084800 scopus 로고    scopus 로고
    • Allyl isothiocyanate as a cancer chemopreventive phytochemical
    • Zhang Y. Allyl isothiocyanate as a cancer chemopreventive phytochemical. Mol. Nutr. Food Res. 2010, 54:127-135.
    • (2010) Mol. Nutr. Food Res. , vol.54 , pp. 127-135
    • Zhang, Y.1
  • 54
    • 33845904129 scopus 로고    scopus 로고
    • The diethary isothiocyanate sulforaphane is antagonist of the human steroid and xenobiotic nuclear receptor
    • Zhou C., Poulton E., Grun F., Bammler T.K., Blumberg B., Thummel E., Eaton D.L. The diethary isothiocyanate sulforaphane is antagonist of the human steroid and xenobiotic nuclear receptor. Mol. Pharmacol. 2007, 71:220-229.
    • (2007) Mol. Pharmacol. , vol.71 , pp. 220-229
    • Zhou, C.1    Poulton, E.2    Grun, F.3    Bammler, T.K.4    Blumberg, B.5    Thummel, E.6    Eaton, D.L.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.