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Volumn 19, Issue 11, 2013, Pages 2952-2961

Colon cancer-specific cytochrome P450 2W1 converts duocarmycin analogues into potent tumor cytotoxins

Author keywords

[No Author keywords available]

Indexed keywords

(5 CHLORO 1H INDOL 2 YL)[1 (CHLOROMETHYL) 1,2 DIHYDROPYRROLO[3,2 E]INDOL 3(6H) YL] METHANONE; [1 (CHLOROMETHYL) 1,2 DIHYDROPYRROLO[3,2 E]INDOL 3 (6H) YL](5 FLURO 1H INDOL 2 YL)METHANONE; [8 (CHLOROMETHYL) 7,8 DIHYDRO 6H FURO[3,2 E]INDOL 6 YL](5 FLURO 1H INDOL 2 YL)METHANONE; CYTOCHROME P450; CYTOCHROME P450 2W1; DOXORUBICIN; DUOCARMYCIN DERIVATIVE; HISTONE H2AX; ICT 2705; ICT 2706; ICT 2726; UNCLASSIFIED DRUG;

EID: 84878999256     PISSN: 10780432     EISSN: 15573265     Source Type: Journal    
DOI: 10.1158/1078-0432.CCR-13-0238     Document Type: Article
Times cited : (50)

References (28)
  • 1
    • 84859241733 scopus 로고    scopus 로고
    • Advances in the understanding and treatment of colorectal cancer
    • Soreide K, Berg M, Skudal BS, Nedreboe BS. Advances in the understanding and treatment of colorectal cancer. Discov Med 2011; 12:393-404.
    • (2011) Discov Med , vol.12 , pp. 393-404
    • Soreide, K.1    Berg, M.2    Skudal, B.S.3    Nedreboe, B.S.4
  • 3
    • 34548277030 scopus 로고    scopus 로고
    • Survival for eight major cancers and all cancers combined for European adults diagnosed in 1995-99: results of the EUROCARE-4 study
    • DOI 10.1016/S1470-2045(07)70245-0, PII S1470204507702450
    • Berrino F, De Angelis R, Sant M, Rosso S, Bielska-Lasota M, Coebergh JW, et al. Survival for eight major cancers and all cancers combined for European adults diagnosed in 1995-99: results of the EUROCARE-4 study. Lancet Oncol 2007;8:773-83. (Pubitemid 47321600)
    • (2007) Lancet Oncology , vol.8 , Issue.9 , pp. 773-783
    • Berrino, F.1    De Angelis, R.2    Sant, M.3    Rosso, S.4    Lasota, M.B.5    Coebergh, J.W.6    Santaquilani, M.7
  • 4
    • 37149011176 scopus 로고    scopus 로고
    • Cytochrome P450s in the development of target-based anticancer drugs
    • DOI 10.1016/j.canlet.2007.10.024, PII S0304383507005095
    • Purnapatre K, Khattar SK, Saini KS. Cytochrome P450s in the development of target-based anticancer drugs. Cancer Lett 2008; 259:1-15. (Pubitemid 350253101)
    • (2008) Cancer Letters , vol.259 , Issue.1 , pp. 1-15
    • Purnapatre, K.1    Khattar, S.K.2    Saini, K.S.3
  • 5
    • 77449136592 scopus 로고    scopus 로고
    • Molecular genetics and epigenetics of the cytochrome P450 gene family and its relevance for cancer risk and treatment
    • Rodriguez-Antona C, Gomez A, Karlgren M, Sim SC, Ingelman-Sundberg M. Molecular genetics and epigenetics of the cytochrome P450 gene family and its relevance for cancer risk and treatment. Hum Genet 2010;127:1-17.
    • (2010) Hum Genet , vol.127 , pp. 1-17
    • Rodriguez-Antona, C.1    Gomez, A.2    Karlgren, M.3    Sim, S.C.4    Ingelman-Sundberg, M.5
  • 6
    • 30644478786 scopus 로고    scopus 로고
    • Activation of oxazaphosphorines by cytochrome P450: Application to gene-directed enzyme prodrug therapy for cancer
    • DOI 10.1016/j.tiv.2005.06.046, PII S0887233305002079
    • Roy P, Waxman DJ. Activation of oxazaphosphorines by cytochrome P450: application to gene-directed enzyme prodrug therapy for cancer. Toxicol In Vitro 2006;20:176-86. (Pubitemid 43087701)
    • (2006) Toxicology in Vitro , vol.20 , Issue.2 , pp. 176-186
    • Roy, P.1    Waxman, D.J.2
  • 7
    • 82055176666 scopus 로고    scopus 로고
    • Prodrugs for targeted tumor therapies: Recent developments in ADEPT, GDEPT and PMT
    • Tietze LF, Schmuck K. Prodrugs for targeted tumor therapies: recent developments in ADEPT, GDEPT and PMT. Curr Pharm Des 2011; 17:3527-47.
    • (2011) Curr Pharm des , vol.17 , pp. 3527-3547
    • Tietze, L.F.1    Schmuck, K.2
  • 8
    • 57649091896 scopus 로고    scopus 로고
    • Preclinical toxicokinetic evaluation of phortress [2-(4-amino-3- methylphenyl)-5-fluorobenzothiazole lysylamide dihydrochloride] in two rodent species
    • Bradshaw TD, Wren JE, Bruce M, Barrett DA, Leong CO, Gaskell M, et al. Preclinical toxicokinetic evaluation of phortress [2-(4-amino-3-methylphenyl)-5- fluorobenzothiazole lysylamide dihydrochloride] in two rodent species. Pharmacology 2009;83:99-109.
    • (2009) Pharmacology , vol.83 , pp. 99-109
    • Bradshaw, T.D.1    Wren, J.E.2    Bruce, M.3    Barrett, D.A.4    Leong, C.O.5    Gaskell, M.6
  • 9
    • 33646463990 scopus 로고    scopus 로고
    • Cytochrome P450 1B1: A novel anticancer therapeutic target
    • McFadyen MC, Murray GI. Cytochrome P450 1B1: a novel anticancer therapeutic target. Future Oncol 2005;1:259-63.
    • (2005) Future Oncol , vol.1 , pp. 259-263
    • McFadyen, M.C.1    Murray, G.I.2
  • 12
    • 60349099759 scopus 로고    scopus 로고
    • The expression of the novel CYP2W1 enzyme is an independent prognostic factor in colorectal cancer - A pilot study
    • Edler D, Stenstedt K, Ohrling K, Hallstrom M, Karlgren M, Ingelman-Sundberg M, et al. The expression of the novel CYP2W1 enzyme is an independent prognostic factor in colorectal cancer - a pilot study. Eur J Cancer 2009;45:705-12.
    • (2009) Eur J Cancer , vol.45 , pp. 705-712
    • Edler, D.1    Stenstedt, K.2    Ohrling, K.3    Hallstrom, M.4    Karlgren, M.5    Ingelman-Sundberg, M.6
  • 14
    • 78649931848 scopus 로고    scopus 로고
    • Colorectal cancer-specific cytochrome P450 2W1: Intracellular localization, glycosylation, and catalytic activity
    • Gomez A, Nekvindova J, Travica S, Lee MY, Johansson I, Edler D, et al. Colorectal cancer-specific cytochrome P450 2W1: intracellular localization, glycosylation, and catalytic activity. Mol Pharmacol 2010;78:1004-11.
    • (2010) Mol Pharmacol , vol.78 , pp. 1004-1011
    • Gomez, A.1    Nekvindova, J.2    Travica, S.3    Lee, M.Y.4    Johansson, I.5    Edler, D.6
  • 15
    • 80053946627 scopus 로고    scopus 로고
    • CYP2S1 and CYP2W1 mediate 2-(3,4-dimethoxyphenyl)-5-fluorobenzothiazole (GW-610, NSC 721648) sensitivity in breast and colorectal cancer cells
    • Tan BS, Tiong KH, Muruhadas A, Randhawa N, Choo HL, Bradshaw TD, et al. CYP2S1 and CYP2W1 mediate 2-(3,4-dimethoxyphenyl)-5-fluorobenzothiazole (GW-610, NSC 721648) sensitivity in breast and colorectal cancer cells. Mol Cancer Ther 2011;10:1982-92.
    • (2011) Mol Cancer Ther , vol.10 , pp. 1982-1992
    • Tan, B.S.1    Tiong, K.H.2    Muruhadas, A.3    Randhawa, N.4    Choo, H.L.5    Bradshaw, T.D.6
  • 16
    • 84865249231 scopus 로고    scopus 로고
    • Bioactivation of fluorinated 2-aryl-benzothiazole antitumor molecules by human cytochrome P450s 1A1 and 2W1 and deactivation by cytochrome P450 2S1
    • Wang K, Guengerich FP. Bioactivation of fluorinated 2-aryl-benzothiazole antitumor molecules by human cytochrome P450s 1A1 and 2W1 and deactivation by cytochrome P450 2S1. Chem Res Toxicol 2012; 25:1740-51.
    • (2012) Chem Res Toxicol , vol.25 , pp. 1740-1751
    • Wang, K.1    Guengerich, F.P.2
  • 17
    • 33745137491 scopus 로고    scopus 로고
    • Recombinant enzymes overexpressed in bacteria show broad catalytic specificity of human cytochrome P450 2W1 and limited activity of human cytochrome P450 2S1
    • DOI 10.1124/mol.106.023648
    • Wu ZL, Sohl CD, Shimada T, Guengerich FP. Recombinant enzymes overexpressed in bacteria show broad catalytic specificity of human cytochrome P450 2W1 and limited activity of human cytochrome P450 2S1. Mol Pharmacol 2006;69:2007-14. (Pubitemid 43894320)
    • (2006) Molecular Pharmacology , vol.69 , Issue.6 , pp. 2007-2014
    • Wu, Z.-L.1    Sohl, C.D.2    Shimada, T.3    Guengerich, F.P.4
  • 19
    • 84863792593 scopus 로고    scopus 로고
    • Metabolomic analysis and identification of a role for the orphan human cytochrome P450 2W1 in selective oxidation of lysophospholipids
    • Xiao Y, Guengerich FP. Metabolomic analysis and identification of a role for the orphan human cytochrome P450 2W1 in selective oxidation of lysophospholipids. J Lipid Res 2012;53:1610-7.
    • (2012) J Lipid Res , vol.53 , pp. 1610-1617
    • Xiao, Y.1    Guengerich, F.P.2
  • 20
    • 80155209663 scopus 로고    scopus 로고
    • Modification of the duocarmycin pharmacophore enables CYP1A1 targeting for biological activity
    • Pors K, Loadman PM, Shnyder SD, Sutherland M, Sheldrake HM, Guino M, et al. Modification of the duocarmycin pharmacophore enables CYP1A1 targeting for biological activity. Chem Commun 2011;47:12062-4.
    • (2011) Chem Commun , vol.47 , pp. 12062-12064
    • Pors, K.1    Loadman, P.M.2    Shnyder, S.D.3    Sutherland, M.4    Sheldrake, H.M.5    Guino, M.6
  • 21
    • 33846209483 scopus 로고    scopus 로고
    • Tumour-specific expression of CYP2W1: Its potential as a drug target in cancer therapy
    • DOI 10.1517/14728222.11.1.61
    • Karlgren M, Ingelman-Sundberg M. Tumour-specific expression of CYP2W1: its potential as a drug target in cancer therapy. Expert Opin Ther Targets 2007;11:61-7. (Pubitemid 46099752)
    • (2007) Expert Opinion on Therapeutic Targets , vol.11 , Issue.1 , pp. 61-67
    • Karlgen, M.1    Ingelman-Sundberg, M.2
  • 22
    • 39549084702 scopus 로고    scopus 로고
    • Overexpression of phosphoserine aminotransferase PSAT1 stimulates cell growth and increases chemoresistance of colon cancer cells
    • Vie N, Copois V, Bascoul-Mollevi C, Denis V, Bec N, Robert B, et al. Overexpression of phosphoserine aminotransferase PSAT1 stimulates cell growth and increases chemoresistance of colon cancer cells. Mol Cancer 2008;7:14.
    • (2008) Mol Cancer , vol.7 , pp. 14
    • Vie, N.1    Copois, V.2    Bascoul-Mollevi, C.3    Denis, V.4    Bec, N.5    Robert, B.6
  • 26
    • 0028936342 scopus 로고
    • Intratumoral activation and enhanced chemotherapeutic effect of oxazaphosphorines following cytochrome P-450 gene transfer: Development of a combined chemotherapy/cancer gene therapy strategy
    • Chen L, Waxman DJ. Intratumoral activation and enhanced chemotherapeutic effect of oxazaphosphorines following cytochrome P-450 gene transfer: development of a combined chemotherapy/cancer gene therapy strategy. Cancer Res 1995;55:581-9.
    • (1995) Cancer Res , vol.55 , pp. 581-589
    • Chen, L.1    Waxman, D.J.2
  • 27
    • 77956463502 scopus 로고    scopus 로고
    • Adenoviral delivery of pan-caspase inhibitor p35 enhances bystander killing by P450 gene-directed enzyme prodrug therapy using cyclophosphamide+
    • Doloff JC, Su T, Waxman DJ. Adenoviral delivery of pan-caspase inhibitor p35 enhances bystander killing by P450 gene-directed enzyme prodrug therapy using cyclophosphamide+. BMC Cancer 2010;10:487.
    • (2010) BMC Cancer , vol.10 , pp. 487
    • Doloff, J.C.1    Su, T.2    Waxman, D.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.