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Volumn 10, Issue 4, 2004, Pages 1492-1499

NADPH Alkenal/One Oxidoreductase Activity Determines Sensitivity of Cancer Cells to the Chemotherapeutic Alkylating Agent Irofulven

Author keywords

[No Author keywords available]

Indexed keywords

ALKYLATING AGENT; ANTINEOPLASTIC AGENT; CYCLOPROPANE DERIVATIVE; CYTOTOXIC AGENT; GLUTATHIONE; ILLUDIN M; ILLUDIN S; IROFULVEN; KETONE DERIVATIVE; OXIDOREDUCTASE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE ALKENAL OXIDOREDUCTASE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE ALKENONE OXIDOREDUCTASE; UNCLASSIFIED DRUG;

EID: 1642293264     PISSN: 10780432     EISSN: None     Source Type: Journal    
DOI: 10.1158/1078-0432.CCR-03-0162     Document Type: Article
Times cited : (41)

References (20)
  • 3
    • 0034961022 scopus 로고    scopus 로고
    • In vivo antitumour efficacy of MGI-114 (6-hydroxymethylacylfulvene, HMAF) in various human tumour xenograft models including several lung and gastric tumours
    • Sato, Y., Kashimoto, S., MacDonald, J. R., and Nakano, K. In vivo antitumour efficacy of MGI-114 (6-hydroxymethylacylfulvene, HMAF) in various human tumour xenograft models including several lung and gastric tumours. Eur. J. Cancer, 37: 1419-1428, 2001.
    • (2001) Eur. J. Cancer , vol.37 , pp. 1419-1428
    • Sato, Y.1    Kashimoto, S.2    MacDonald, J.R.3    Nakano, K.4
  • 6
    • 0033106003 scopus 로고    scopus 로고
    • Enhanced antitumor activity of 6-hydroxymethylacylfulvene in combination with irinotecan and 5-fluorouracil in the HT29 human colon tumor xenograft model
    • Britten, C. D., Hilsenbeck, S. G., Eckhardt, S. G., Marty, J., Mangold, G., MacDonald, J. R., Rowinsky, E. K., Von Hoff, D. D., and Weitman, S. Enhanced antitumor activity of 6-hydroxymethylacylfulvene in combination with irinotecan and 5-fluorouracil in the HT29 human colon tumor xenograft model. Cancer Res., 59: 1049-1053, 1999.
    • (1999) Cancer Res. , vol.59 , pp. 1049-1053
    • Britten, C.D.1    Hilsenbeck, S.G.2    Eckhardt, S.G.3    Marty, J.4    Mangold, G.5    MacDonald, J.R.6    Rowinsky, E.K.7    Von Hoff, D.D.8    Weitman, S.9
  • 8
    • 0029834306 scopus 로고    scopus 로고
    • (Hydroxymethyl)acylfulvene: An illudin derivative with superior antitumor properties
    • McMorris, T. C., Kelner, M. J., Wang, W., Yu, J., Estes, L. A., and Taetle, R. (Hydroxymethyl)acylfulvene: an illudin derivative with superior antitumor properties. J. Nat. Prod., 59: 896-899, 1996.
    • (1996) J. Nat. Prod. , vol.59 , pp. 896-899
    • McMorris, T.C.1    Kelner, M.J.2    Wang, W.3    Yu, J.4    Estes, L.A.5    Taetle, R.6
  • 9
    • 8244228308 scopus 로고
    • Fungal metabolites. The structures of the novel sesquiterpenoids illudin-S and -M
    • McMorris, T. C., and Anchel, M. Fungal metabolites. The structures of the novel sesquiterpenoids illudin-S and -M. J. Am. Chem. Soc., 87: 1594-1600, 1965.
    • (1965) J. Am. Chem. Soc. , vol.87 , pp. 1594-1600
    • McMorris, T.C.1    Anchel, M.2
  • 11
    • 0025168447 scopus 로고
    • Preclinical evaluation of illudins as anticancer agents: Basis for selective cytotoxicity
    • Kelner, M. J., McMorris, T. C., and Taetle, R. Preclinical evaluation of illudins as anticancer agents: basis for selective cytotoxicity. J. Natl. Cancer Inst. (Bethesda), 82: 1562-1565, 1990.
    • (1990) J. Natl. Cancer Inst. (Bethesda) , vol.82 , pp. 1562-1565
    • Kelner, M.J.1    McMorris, T.C.2    Taetle, R.3
  • 13
    • 0025118589 scopus 로고
    • Metabolism of illudin S, a toxic principle of Lampteromyces japonicus, by rat liver. I. Isolation and identification of cyclopropane ring-cleavage metabolites
    • Tanaka, K., Inoue, T., Kadota, S., and Kikuchi, T. Metabolism of illudin S, a toxic principle of Lampteromyces japonicus, by rat liver. I. Isolation and identification of cyclopropane ring-cleavage metabolites. Xenobiotica, 20: 671-681, 1990.
    • (1990) Xenobiotica , vol.20 , pp. 671-681
    • Tanaka, K.1    Inoue, T.2    Kadota, S.3    Kikuchi, T.4
  • 14
    • 0032821945 scopus 로고    scopus 로고
    • Metabolism of antitumor hydroxymethylacylfulvene by rat liver cytosol
    • McMorris, T. C., Elayadi, A. N., Yu, J., Hu, Y., and Kelner, M. J. Metabolism of antitumor hydroxymethylacylfulvene by rat liver cytosol. Drug Metab. Dispos., 27: 983-985, 1999.
    • (1999) Drug Metab. Dispos. , vol.27 , pp. 983-985
    • McMorris, T.C.1    Elayadi, A.N.2    Yu, J.3    Hu, Y.4    Kelner, M.J.5
  • 15
  • 16
    • 0026515575 scopus 로고
    • Metabolism by rat liver cytosol of illudin S, a toxic substance of Lampteromyces japonicus. II. Characterization of illudin S-metabolizing enzyme
    • Tanaka, K., Inoue, T., Kadota, S., and Kikuchi, T. Metabolism by rat liver cytosol of illudin S, a toxic substance of Lampteromyces japonicus. II. Characterization of illudin S-metabolizing enzyme. Xenobiotica, 22: 33-39, 1992.
    • (1992) Xenobiotica , vol.22 , pp. 33-39
    • Tanaka, K.1    Inoue, T.2    Kadota, S.3    Kikuchi, T.4
  • 17
    • 0035798606 scopus 로고    scopus 로고
    • Antioxidative function and substrate specificity of NAD(P)H-dependent alkenal/one oxidoreductase. A new role for leukotriene B4 12-hydroxydehydrogenase/15-oxoprostaglandin 13-reductase
    • Dick, R. A., Kwak, M. K., Sutter, T. R., and Kensler, T. W. Antioxidative function and substrate specificity of NAD(P)H-dependent alkenal/one oxidoreductase. A new role for leukotriene B4 12-hydroxydehydrogenase/15-oxoprostaglandin 13-reductase. J. Biol. Chem., 276: 40803-40810, 2001.
    • (2001) J. Biol. Chem. , vol.276 , pp. 40803-40810
    • Dick, R.A.1    Kwak, M.K.2    Sutter, T.R.3    Kensler, T.W.4
  • 18
    • 0023130372 scopus 로고
    • Evaluation of a tetrazolium-based semiautomated colorimetric assay: Assessment of chemosensitivity testing
    • Carmichael, J., DeGraff, W. G., Gazdar, A. F., Minna, J. D., and Mitchell, J. B. Evaluation of a tetrazolium-based semiautomated colorimetric assay: assessment of chemosensitivity testing. Cancer Res., 47: 936-942, 1987.
    • (1987) Cancer Res. , vol.47 , pp. 936-942
    • Carmichael, J.1    DeGraff, W.G.2    Gazdar, A.F.3    Minna, J.D.4    Mitchell, J.B.5
  • 19
    • 0035699829 scopus 로고    scopus 로고
    • Biological reactive intermediates in drug discovery and development: A perspective from the pharmaceutical industry
    • Baillie, T. A., and Kassahun, K. Biological reactive intermediates in drug discovery and development: a perspective from the pharmaceutical industry. Adv. Exp. Med. Biol., 500: 45-51, 2001.
    • (2001) Adv. Exp. Med. Biol. , vol.500 , pp. 45-51
    • Baillie, T.A.1    Kassahun, K.2
  • 20
    • 0030068919 scopus 로고    scopus 로고
    • cDNA cloning, expression, and mutagenesis study of leukotriene B4 12-hydroxydehydrogenase
    • Yokomizo, T., Ogawa, Y., Uozumi, N., Kume, K., Izumi, T., and Shimizu, T. cDNA cloning, expression, and mutagenesis study of leukotriene B4 12-hydroxydehydrogenase. J. Biol. Chem., 271: 2844-2850, 1996.
    • (1996) J. Biol. Chem. , vol.271 , pp. 2844-2850
    • Yokomizo, T.1    Ogawa, Y.2    Uozumi, N.3    Kume, K.4    Izumi, T.5    Shimizu, T.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.