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Volumn 414, Issue , 1997, Pages 155-169

Yeast aldehyde dehydrogenase sensitivity to inhibition by chlorpropamide analogues as an indicator of human aldehyde dehydrogenase sensitivity to these agents

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE DEHYDROGENASE; CHLORPROPAMIDE;

EID: 0031002301     PISSN: 00652598     EISSN: None     Source Type: Book Series    
DOI: None     Document Type: Conference Paper
Times cited : (7)

References (49)
  • 1
    • 0024534840 scopus 로고
    • Nomenclature of mammalian aldehyde dehydrogenases
    • Anonymous: Nomenclature of mammalian aldehyde dehydrogenases. Prog. Clin. Biol. Res. 290 (1989) xix-xxi.
    • (1989) Prog. Clin. Biol. Res. , vol.290
  • 2
    • 0026539553 scopus 로고
    • Aldehyde dehydrogenase. Covalent intermediate in aldehyde dehydrogenation and ester hydrolysis
    • Blatter, E.E., Abriola, D.P. and Pietruszko, R.: Aldehyde dehydrogenase. Covalent intermediate in aldehyde dehydrogenation and ester hydrolysis. Biochem. J. 282 (1992) 353-360.
    • (1992) Biochem. J. , vol.282 , pp. 353-360
    • Blatter, E.E.1    Abriola, D.P.2    Pietruszko, R.3
  • 3
    • 0018077763 scopus 로고
    • Kinetics and reaction mechanism of potassium-activated aldehyde dehydrogenase from Saccharomyces cerevisiae
    • Bostian, K.A. and Betts, G.F.: Kinetics and reaction mechanism of potassium-activated aldehyde dehydrogenase from Saccharomyces cerevisiae. Biochem. J. 173 (1978) 787-798.
    • (1978) Biochem. J. , vol.173 , pp. 787-798
    • Bostian, K.A.1    Betts, G.F.2
  • 4
    • 0017184389 scopus 로고
    • A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding
    • Bradford, M.M.: A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 72 (1976) 248-254.
    • (1976) Anal. Biochem. , vol.72 , pp. 248-254
    • Bradford, M.M.1
  • 5
    • 0344934175 scopus 로고
    • Aldehyde dehydrogenase inhibitors as alcohol-sensitizing drugs: A pharmacological perspective
    • Brien, J.F. and Loomis, C.W.: Aldehyde dehydrogenase inhibitors as alcohol-sensitizing drugs: a pharmacological perspective. Trends Pharmacol. Sci. (1985) 477-480.
    • (1985) Trends Pharmacol. Sci. , pp. 477-480
    • Brien, J.F.1    Loomis, C.W.2
  • 6
    • 0029936167 scopus 로고    scopus 로고
    • Protection by transfected rat or human class 3 aldehyde dehydrogenases against the cytotoxic effects of oxazaphosphorine alkylating agents in hamster V79 cell lines
    • Bunting, K.D. and Townsend, A.J.: Protection by transfected rat or human class 3 aldehyde dehydrogenases against the cytotoxic effects of oxazaphosphorine alkylating agents in hamster V79 cell lines. J. Biol. Chem. 271 (1996) 11891-11896.
    • (1996) J. Biol. Chem. , vol.271 , pp. 11891-11896
    • Bunting, K.D.1    Townsend, A.J.2
  • 7
    • 0019742086 scopus 로고
    • Involvement of arginine residue in the phosphate binding site of human placental alkaline phosphatase
    • Chueh, S.-H., Chang, G.-G., Chang, T.-C. and Pan, F.: Involvement of arginine residue in the phosphate binding site of human placental alkaline phosphatase. Int. J. Biochem. 13 (1981) 1143-1149.
    • (1981) Int. J. Biochem. , vol.13 , pp. 1143-1149
    • Chueh, S.-H.1    Chang, G.-G.2    Chang, T.-C.3    Pan, F.4
  • 8
    • 0023656292 scopus 로고
    • +-activated aldehyde dehydrogenase of Saccharomyces cerevisiae
    • +-activated aldehyde dehydrogenase of Saccharomyces cerevisiae. Biochem. J. 247 (1987) 377-384.
    • (1987) Biochem. J. , vol.247 , pp. 377-384
    • Dickinson, F.M.1    Haywood, G.W.2
  • 9
    • 0026667068 scopus 로고
    • Identification of human liver aldehyde dehydrogenases that catalyze the oxidation of aldophosphamide and retinaldehyde
    • Dockham, P.A., Lee, M.-O. and Sladek, N.E.: Identification of human liver aldehyde dehydrogenases that catalyze the oxidation of aldophosphamide and retinaldehyde. Biochem. Pharmacol. 43 (1992) 2453-2469.
    • (1992) Biochem. Pharmacol. , vol.43 , pp. 2453-2469
    • Dockham, P.A.1    Lee, M.-O.2    Sladek, N.E.3
  • 10
    • 0028961395 scopus 로고
    • Investigation of the active site cysteine residue of rat liver mitochondrial aldehyde dehydrogenase by site-directed mutagenesis
    • Farrés, J., Wang, T.T.Y., Cunningham, S.J. and Weiner, H.: Investigation of the active site cysteine residue of rat liver mitochondrial aldehyde dehydrogenase by site-directed mutagenesis. Biochemistry 34 (1995) 2592-2598.
    • (1995) Biochemistry , vol.34 , pp. 2592-2598
    • Farrés, J.1    Wang, T.T.Y.2    Cunningham, S.J.3    Weiner, H.4
  • 11
    • 0015499994 scopus 로고
    • Horse liver aldehyde dehydrogenase. II. Kinetic and mechanistic implications of the dehydrogenase and esterase activity
    • Feldman, R.I. and Weiner, H.: Horse liver aldehyde dehydrogenase. II. Kinetic and mechanistic implications of the dehydrogenase and esterase activity. J. Biol. Chem. 247 (1972) 267-272.
    • (1972) J. Biol. Chem. , vol.247 , pp. 267-272
    • Feldman, R.I.1    Weiner, H.2
  • 12
    • 0025019083 scopus 로고
    • Pharmacogenetics of aldehyde dehydrogenase (ALDH)
    • Goedde, H.W. and Agarwal, D.P.: Pharmacogenetics of aldehyde dehydrogenase (ALDH). Pharmacol. Ther. 45 (1990) 345-371.
    • (1990) Pharmacol. Ther. , vol.45 , pp. 345-371
    • Goedde, H.W.1    Agarwal, D.P.2
  • 13
    • 0025803664 scopus 로고
    • Identification of a catalytically essential nucleophilic residue in sheep liver cytoplasmic aldehyde dehydrogenase
    • Kitson, T.M., Hill, J.P. and Midwinter, G.G.: Identification of a catalytically essential nucleophilic residue in sheep liver cytoplasmic aldehyde dehydrogenase. Biochem. J. 275 (1991) 207-210.
    • (1991) Biochem. J. , vol.275 , pp. 207-210
    • Kitson, T.M.1    Hill, J.P.2    Midwinter, G.G.3
  • 14
    • 0029935028 scopus 로고    scopus 로고
    • Possible role of liver cytosolic and mitochondrial aldehyde dehydrogenases in acetaldehyde metabolism
    • Klyosov, A.A., Rashkovetsky, L.G., Tahir, M.K. and Keung, W.-M: Possible role of liver cytosolic and mitochondrial aldehyde dehydrogenases in acetaldehyde metabolism. Biochemistry 35 (1996) 4445-4456.
    • (1996) Biochemistry , vol.35 , pp. 4445-4456
    • Klyosov, A.A.1    Rashkovetsky, L.G.2    Tahir, M.K.3    Keung, W.-M.4
  • 15
    • 0025865480 scopus 로고
    • The cytosolic and glycosomal glyceraldehyde-3-phosphate dehydrogenase from Trypanosoma brucei. Kinetic properties and comparison with homologous enzymes
    • Lambeir, A.-M., Loiseau, A.M., Kuntz, D.A., Vellieux, F.M., Michels, P.A.M. and Opperdoes, F.R.: The cytosolic and glycosomal glyceraldehyde-3-phosphate dehydrogenase from Trypanosoma brucei. Kinetic properties and comparison with homologous enzymes. Eur. J. Biochem. 198 (1991) 429-435.
    • (1991) Eur. J. Biochem. , vol.198 , pp. 429-435
    • Lambeir, A.-M.1    Loiseau, A.M.2    Kuntz, D.A.3    Vellieux, F.M.4    Michels, P.A.M.5    Opperdoes, F.R.6
  • 16
    • 0026616787 scopus 로고
    • 1-Hydroxylated derivatives of chlorpropamide and its analogs as inhibitors of aldehyde dehydrogenase in vivo
    • 1-Hydroxylated derivatives of chlorpropamide and its analogs as inhibitors of aldehyde dehydrogenase in vivo. J. Med. Chem. 35 (1992a) 3641-3647.
    • (1992) J. Med. Chem. , vol.35 , pp. 3641-3647
    • Lee, M.J.C.1    Elberling, J.A.2    Nagasawa, H.T.3
  • 17
  • 18
    • 0026655335 scopus 로고
    • Aldehyde dehydrogenases and their role in carcinogenesis
    • Lindahl, R.: Aldehyde dehydrogenases and their role in carcinogenesis. Crit. Rev. Biochem. Mol. Biol. 27 (1992) 283-335.
    • (1992) Crit. Rev. Biochem. Mol. Biol. , vol.27 , pp. 283-335
    • Lindahl, R.1
  • 19
    • 0025777891 scopus 로고
    • Aldehyde dehydrogenases: What can be learned from a baker's dozen sequences
    • Lindahl, R. and Hempel, J.: Aldehyde dehydrogenases: what can be learned from a baker's dozen sequences. Adv. Exp. Med. Biol. 284 (1990) 1-8.
    • (1990) Adv. Exp. Med. Biol. , vol.284 , pp. 1-8
    • Lindahl, R.1    Hempel, J.2
  • 20
    • 0022361705 scopus 로고
    • Effect of tolbutamide and chlorpropamide on acetaldehyde metabolism in two inbred strains of mice
    • Little, R.G. II and Petersen, D.R.: Effect of tolbutamide and chlorpropamide on acetaldehyde metabolism in two inbred strains of mice. Toxicol. Appl. Pharmacol. 80 (1985) 206-214.
    • (1985) Toxicol. Appl. Pharmacol. , vol.80 , pp. 206-214
    • Little II, R.G.1    Petersen, D.R.2
  • 21
  • 22
    • 0029685930 scopus 로고    scopus 로고
    • Overexpression of the human aldehyde dehydrogenase class I results in increased resistance to 4-hydroperoxycyclophosphamide
    • Moreb, J., Schweder, M., Suresh, A. and Zucali, J.R.: Overexpression of the human aldehyde dehydrogenase class I results in increased resistance to 4-hydroperoxycyclophosphamide. Cancer Gene Ther. 3 (1996) 24-30.
    • (1996) Cancer Gene Ther. , vol.3 , pp. 24-30
    • Moreb, J.1    Schweder, M.2    Suresh, A.3    Zucali, J.R.4
  • 23
    • 0026478526 scopus 로고
    • Human mitochondrial aldehyde dehydrogenase substrate specificity: Comparison of esterase with dehydrogenase reaction
    • Mukerjee, N. and Pietruszko, R.: Human mitochondrial aldehyde dehydrogenase substrate specificity: comparison of esterase with dehydrogenase reaction. Arch. Biochem. Biophys. 299 (1992) 23-29.
    • (1992) Arch. Biochem. Biophys. , vol.299 , pp. 23-29
    • Mukerjee, N.1    Pietruszko, R.2
  • 24
    • 0028086127 scopus 로고
    • Inactivation of human aldehyde dehydrogenase by isosorbide dinitrate
    • Mukerjee, N. and Pietruszko, R.: Inactivation of human aldehyde dehydrogenase by isosorbide dinitrate. J. Biol. Chem. 269 (1994) 21664-21669.
    • (1994) J. Biol. Chem. , vol.269 , pp. 21664-21669
    • Mukerjee, N.1    Pietruszko, R.2
  • 25
    • 0022415188 scopus 로고
    • Structure vs. activity in the sulfonylurea-mediated disulfiram-ethanol reaction
    • Nagasawa, H.T., DeMaster, E.G., Kwon, C.-H., Fraser, P.S. and Shirota, F.N.: Structure vs. activity in the sulfonylurea-mediated disulfiram-ethanol reaction. Alcohol 2 (1985) 123-128.
    • (1985) Alcohol , vol.2 , pp. 123-128
    • Nagasawa, H.T.1    DeMaster, E.G.2    Kwon, C.-H.3    Fraser, P.S.4    Shirota, F.N.5
  • 28
    • 0029030350 scopus 로고
    • Prodrugs of nitroxyl as potential aldehyde dehydrogenase inhibitors vis-à-vis vascular smooth muscle relaxants
    • Nagasawa, H.T., Kawle, S.P., Elberling, J.A., DeMaster, E.G. and Fukuto, J.M.: Prodrugs of nitroxyl as potential aldehyde dehydrogenase inhibitors vis-à-vis vascular smooth muscle relaxants. J. Med. Chem. 38 (1995) 1865-1871.
    • (1995) J. Med. Chem. , vol.38 , pp. 1865-1871
    • Nagasawa, H.T.1    Kawle, S.P.2    Elberling, J.A.3    DeMaster, E.G.4    Fukuto, J.M.5
  • 29
    • 0019916102 scopus 로고
    • Chlorpropamide-alcohol flushing, aldehyde dehydrogenase activity, and diabetic complications
    • Öhlin, H., Jerntorp, P., Bergström, B. and Almér, L-O.: Chlorpropamide-alcohol flushing, aldehyde dehydrogenase activity, and diabetic complications. Brit. Med. J. 285 (1982) 838-840.
    • (1982) Brit. Med. J. , vol.285 , pp. 838-840
    • Öhlin, H.1    Jerntorp, P.2    Bergström, B.3    Almér, L.-O.4
  • 30
    • 0019812327 scopus 로고
    • A review of the clinical use of disulfiram and calcium carbimide in alcoholism treatment
    • Peachey, J.E.: A review of the clinical use of disulfiram and calcium carbimide in alcoholism treatment. J. Clin. Psychopharmacol. 1 (1981) 368-375.
    • (1981) J. Clin. Psychopharmacol. , vol.1 , pp. 368-375
    • Peachey, J.E.1
  • 31
    • 0026469942 scopus 로고
    • The pharmacology and toxicology of disulfiram and its metabolites
    • Petersen, E.N.: The pharmacology and toxicology of disulfiram and its metabolites. Acta Psychiatr. Scand. 86 (1992) 7-13.
    • (1992) Acta Psychiatr. Scand. , vol.86 , pp. 7-13
    • Petersen, E.N.1
  • 32
    • 0030949770 scopus 로고    scopus 로고
    • Inhibition of human class 3 aldehyde dehydrogenase, and sensitization of tumor cells that express significant amounts of this enzyme to oxazaphosphorines, by the naturally occuring compound gossypol
    • Weiner, H., Lindahl, R., Crabb, D.W. and Flynn, T.G. (Eds.) Plenum Press, New York
    • Rekha, G.K. and Sladek, N.E.: Inhibition of human class 3 aldehyde dehydrogenase, and sensitization of tumor cells that express significant amounts of this enzyme to oxazaphosphorines, by the naturally occuring compound gossypol. In Weiner, H., Lindahl, R., Crabb, D.W. and Flynn, T.G. (Eds.) Enzymology and Molecular Biology of Carbonyl Metabolism - 6, Plenum Press, New York, 1997.
    • (1997) Enzymology and Molecular Biology of Carbonyl Metabolism - 6
    • Rekha, G.K.1    Sladek, N.E.2
  • 33
    • 0028134625 scopus 로고
    • Intrinsic cellular resistance to oxazaphosphorines exhibited by a human colon carcinoma cell line expressing relatively large amounts of a class-3 aldehyde dehydrogenase
    • Rekha, G.K., Sreerama, L. and Sladek, N.E.: Intrinsic cellular resistance to oxazaphosphorines exhibited by a human colon carcinoma cell line expressing relatively large amounts of a class-3 aldehyde dehydrogenase. Biochem. Pharmacol. 48 (1994) 1943-1952.
    • (1994) Biochem. Pharmacol. , vol.48 , pp. 1943-1952
    • Rekha, G.K.1    Sreerama, L.2    Sladek, N.E.3
  • 34
    • 0025909284 scopus 로고
    • Molecular cloning of the mitochondrial aldehyde dehydrogenase gene of Saccharomyces cerevisiae by genetic complementation
    • Saigal, D., Cunningham, S.J., Farrés, J. and Weiner, H.: Molecular cloning of the mitochondrial aldehyde dehydrogenase gene of Saccharomyces cerevisiae by genetic complementation. J. Bacteriol. 173 (1991) 3199-3208.
    • (1991) J. Bacteriol. , vol.173 , pp. 3199-3208
    • Saigal, D.1    Cunningham, S.J.2    Farrés, J.3    Weiner, H.4
  • 37
    • 0016713060 scopus 로고
    • Human liver aldehyde dehydrogenase. Esterase activity
    • Sidhu, R.S. and Blair, A.H.: Human liver aldehyde dehydrogenase. Esterase activity. J. Biol. Chem. 250 (1975) 7894-7898.
    • (1975) J. Biol. Chem. , vol.250 , pp. 7894-7898
    • Sidhu, R.S.1    Blair, A.H.2
  • 38
    • 0001358252 scopus 로고
    • Oxazaphosphorine-specific acquired cellular resistance
    • Teicher, B.A. (Ed.). Marcel Dekker, N.Y.
    • Sladek, N.E.: Oxazaphosphorine-specific acquired cellular resistance. In Teicher, B.A. (Ed.). Drug Resistance in Oncology, Marcel Dekker, N.Y., 1993, pp. 375-411.
    • (1993) Drug Resistance in Oncology , pp. 375-411
    • Sladek, N.E.1
  • 39
    • 0001908456 scopus 로고
    • Metabolism and pharmacokinetic behavior of cyclophosphamide and related oxazaphosphorines
    • Powis, G. (Ed.), Pergamon Press, United Kingdom
    • Sladek, N.E.: Metabolism and pharmacokinetic behavior of cyclophosphamide and related oxazaphosphorines. In Powis, G. (Ed.), Anticancer Drugs: Reactive Metabolism and Drug Interactions, Pergamon Press, United Kingdom, 1994, pp. 79-156.
    • (1994) Anticancer Drugs: Reactive Metabolism and Drug Interactions , pp. 79-156
    • Sladek, N.E.1
  • 41
    • 0029039241 scopus 로고
    • Constitutive and overexpressed human cytosolic class-3 aldehyde dehydrogenases in normal and neoplastic cells/secretions
    • Sladek, N.E., Sreerama, L. and Rekha, G.K.: Constitutive and overexpressed human cytosolic class-3 aldehyde dehydrogenases in normal and neoplastic cells/secretions. Adv. Exp. Med. Biol. 372 (1995) 103-114.
    • (1995) Adv. Exp. Med. Biol. , vol.372 , pp. 103-114
    • Sladek, N.E.1    Sreerama, L.2    Rekha, G.K.3
  • 42
    • 0027300380 scopus 로고
    • Identification and characterization of a novel class 3 aldehyde dehydrogenase overexpressed in a human breast adenocarcinoma cell line exhibiting oxazaphosphorine-specific acquired resistance
    • Sreerama, L. and Sladek, N.E.: Identification and characterization of a novel class 3 aldehyde dehydrogenase overexpressed in a human breast adenocarcinoma cell line exhibiting oxazaphosphorine-specific acquired resistance. Biochem. Pharmacol. 45 (1993) 2487-2505.
    • (1993) Biochem. Pharmacol. , vol.45 , pp. 2487-2505
    • Sreerama, L.1    Sladek, N.E.2
  • 43
    • 0028297880 scopus 로고
    • Identification of a methylcholanthrene-induced aldehyde dehydrogenase in a human breast adenocarcinoma cell line exhibiting oxazaphosphorine-specific acquired resistance
    • Sreerama, L. and Sladek, N.E.: Identification of a methylcholanthrene-induced aldehyde dehydrogenase in a human breast adenocarcinoma cell line exhibiting oxazaphosphorine-specific acquired resistance. Cancer Res. 54 (1994) 2176-2185.
    • (1994) Cancer Res. , vol.54 , pp. 2176-2185
    • Sreerama, L.1    Sladek, N.E.2
  • 44
    • 0028832599 scopus 로고
    • Human breast adenocarcinoma MCF-7/0 cells electroporated with cytosolic class 3 aldehyde dehydrogenases obtained from tumor cells and normal tissue exhibit differential sensitivity to mafosfamide
    • Sreerama, L. and Sladek, N.E.: Human breast adenocarcinoma MCF-7/0 cells electroporated with cytosolic class 3 aldehyde dehydrogenases obtained from tumor cells and normal tissue exhibit differential sensitivity to mafosfamide. Drug Metab. Dispos. 23 (1995) 1080-1084.
    • (1995) Drug Metab. Dispos. , vol.23 , pp. 1080-1084
    • Sreerama, L.1    Sladek, N.E.2
  • 45
    • 0030961976 scopus 로고    scopus 로고
    • Class 1 and class 3 aldehyde dehydrogenase levels in the human tumor cell lines currently used by the National Cancer Institute to screen for potentially useful antitumor agents
    • Weiner, H., Lindahl, R., Crabb, D.W. and Flynn, T.G. (Eds.) Plenum Press, New York
    • Sreerama, L. and Sladek, N.E.: Class 1 and class 3 aldehyde dehydrogenase levels in the human tumor cell lines currently used by the National Cancer Institute to screen for potentially useful antitumor agents. In Weiner, H., Lindahl, R., Crabb, D.W. and Flynn, T.G. (Eds.) Enzymology and Molecular Biology of Carbonyl Metabolism - 6, Plenum Press, New York, 1997.
    • (1997) Enzymology and Molecular Biology of Carbonyl Metabolism - 6
    • Sreerama, L.1    Sladek, N.E.2
  • 46
    • 0028946528 scopus 로고
    • Phenolic antioxidant-induced overexpression of class-3 aldehyde dehydrogenase and oxazaphosphorine-specific resistance
    • Sreerama, L., Rekha, G.K. and Sladek, N.E.: Phenolic antioxidant-induced overexpression of class-3 aldehyde dehydrogenase and oxazaphosphorine-specific resistance. Biochem. Pharmacol. 49 (1995) 669-675.
    • (1995) Biochem. Pharmacol. , vol.49 , pp. 669-675
    • Sreerama, L.1    Rekha, G.K.2    Sladek, N.E.3
  • 47
    • 0022657814 scopus 로고
    • Activation and inhibition of yeast aldehyde dehydrogenase activity by pantethine and its metabolites
    • Watanabe, A., Hobara, N. and Nagashima, H.: Activation and inhibition of yeast aldehyde dehydrogenase activity by pantethine and its metabolites. Ann. Nutr. Metab. 30 (1986) 54-57.
    • (1986) Ann. Nutr. Metab. , vol.30 , pp. 54-57
    • Watanabe, A.1    Hobara, N.2    Nagashima, H.3
  • 48
    • 0005499841 scopus 로고
    • Statistical estimations in enzyme kinetics
    • Wilkinson, G.N.: Statistical estimations in enzyme kinetics. Biochem. J. 80 (1961) 324-332.
    • (1961) Biochem. J. , vol.80 , pp. 324-332
    • Wilkinson, G.N.1
  • 49
    • 0027267937 scopus 로고
    • Cloning and expression of the full-length cDNAs encoding human liver class 1 and class 2 aldehyde dehydrogenases
    • Zheng, C.-F., Wang, T.T.Y. and Weiner, H.: Cloning and expression of the full-length cDNAs encoding human liver class 1 and class 2 aldehyde dehydrogenases. Alcohol. Clin. Exp. Res. 17 (1993) 828-831.
    • (1993) Alcohol. Clin. Exp. Res. , vol.17 , pp. 828-831
    • Zheng, C.-F.1    Wang, T.T.Y.2    Weiner, H.3


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