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Volumn 56, Issue 15, 2013, Pages 6273-6277

Re-engineering of the duocarmycin structural architecture enables bioprecursor development targeting CYP1A1 and CYP2W1 for biological activity

Author keywords

[No Author keywords available]

Indexed keywords

CYP2W1; CYTOCHROME; CYTOCHROME P450 1A1; DUOCARMYCIN DERIVATIVE; UNCLASSIFIED DRUG;

EID: 84881439741     PISSN: 00222623     EISSN: 15204804     Source Type: Journal    
DOI: 10.1021/jm4000209     Document Type: Article
Times cited : (37)

References (25)
  • 2
    • 27944433467 scopus 로고    scopus 로고
    • CYP1A1 and CYP1B1 polymorphisms and risk of lung cancer among never smokers: A population-based study
    • Wenzlaff, A. S.; Cote, M. L.; Bock, C. H.; Santer, S. K.; Schwartz, D. R.; Schwartz, A. G. CYP1A1 and CYP1B1 polymorphisms and risk of lung cancer among never smokers: a population-based study Carcinogenesis 2005, 26, 2207-2212
    • (2005) Carcinogenesis , vol.26 , pp. 2207-2212
    • Wenzlaff, A.S.1    Cote, M.L.2    Bock, C.H.3    Santer, S.K.4    Schwartz, D.R.5    Schwartz, A.G.6
  • 3
    • 18144383865 scopus 로고    scopus 로고
    • Overexpression of cytochrome P450 1A1 and its novel spliced variant in ovarian cancer cells: Alternative subcellular enzyme compartmentation may contribute to carcinogenesis
    • Leung, Y. K.; Lau, K. M.; Mobley, J.; Jiang, Z.; Ho, S. M. Overexpression of cytochrome P450 1A1 and its novel spliced variant in ovarian cancer cells: alternative subcellular enzyme compartmentation may contribute to carcinogenesis Cancer Res. 2005, 65, 3726-3734
    • (2005) Cancer Res. , vol.65 , pp. 3726-3734
    • Leung, Y.K.1    Lau, K.M.2    Mobley, J.3    Jiang, Z.4    Ho, S.M.5
  • 4
    • 33645116164 scopus 로고    scopus 로고
    • Cytochrome P450 pharmacogenetics and cancer
    • Rodriguez-Antona, C.; Ingelman-Sundberg, M. Cytochrome P450 pharmacogenetics and cancer Oncogene 2006, 25, 1679-1691
    • (2006) Oncogene , vol.25 , pp. 1679-1691
    • Rodriguez-Antona, C.1    Ingelman-Sundberg, M.2
  • 5
    • 0036015562 scopus 로고    scopus 로고
    • Tumour cytochrome P450 and drug activation
    • Patterson, L. H.; Murray, G. I. Tumour cytochrome P450 and drug activation Curr. Pharm. Des. 2002, 8, 1335-1347
    • (2002) Curr. Pharm. Des. , vol.8 , pp. 1335-1347
    • Patterson, L.H.1    Murray, G.I.2
  • 6
    • 4444223732 scopus 로고    scopus 로고
    • Cytochrome P450 enzymes: Novel options for cancer therapeutics
    • McFadyen, M. C.; Melvin, W. T.; Murray, G. I. Cytochrome P450 enzymes: novel options for cancer therapeutics Mol. Cancer Ther. 2004, 3, 363-371
    • (2004) Mol. Cancer Ther. , vol.3 , pp. 363-371
    • McFadyen, M.C.1    Melvin, W.T.2    Murray, G.I.3
  • 10
    • 0029782488 scopus 로고    scopus 로고
    • CC-1065 and the duocarmycins: Understanding their biological function through mechanistic studies
    • Boger, D. L.; Johnson, D. S. CC-1065 and the duocarmycins: understanding their biological function through mechanistic studies Angew. Chem., Int. Ed. Engl. 1996, 35, 1438-1474
    • (1996) Angew. Chem., Int. Ed. Engl. , vol.35 , pp. 1438-1474
    • Boger, D.L.1    Johnson, D.S.2
  • 11
    • 70349641991 scopus 로고    scopus 로고
    • Fundamental relationships between structure, reactivity, and biological activity for the duocarmycins and CC-1065
    • MacMillan, K. S.; Boger, D. L. Fundamental relationships between structure, reactivity, and biological activity for the duocarmycins and CC-1065 J. Med. Chem. 2009, 52, 5771-5780
    • (2009) J. Med. Chem. , vol.52 , pp. 5771-5780
    • MacMillan, K.S.1    Boger, D.L.2
  • 12
    • 0036015565 scopus 로고    scopus 로고
    • Duocarmycins - Nature's prodrugs?
    • Searcey, M. Duocarmycins-nature's prodrugs? Curr. Pharm. Des. 2002, 8, 1375-1389
    • (2002) Curr. Pharm. Des. , vol.8 , pp. 1375-1389
    • Searcey, M.1
  • 13
    • 74249120351 scopus 로고    scopus 로고
    • Chemical and biological explorations of the family of CC-1065 and the duocarmycin natural products
    • Ghosh, N.; Sheldrake, H. M.; Searcey, M.; Pors, K. Chemical and biological explorations of the family of CC-1065 and the duocarmycin natural products Curr. Top. Med. Chem. 2009, 9, 1494-1524
    • (2009) Curr. Top. Med. Chem. , vol.9 , pp. 1494-1524
    • Ghosh, N.1    Sheldrake, H.M.2    Searcey, M.3    Pors, K.4
  • 15
    • 84872550541 scopus 로고    scopus 로고
    • Antitumor activity of a duocarmycin analogue rationalised to be metabolically activated by cytochrome P450 1a1 in human transitional carcinoma of the bladder
    • Sutherland, M.; Gill, J.; Loadman, P. M.; Sheldrake, H.; Searcey, M.; Pors, K.; Shnyder, S. D.; Patterson, L. H. Antitumor activity of a duocarmycin analogue rationalised to be metabolically activated by cytochrome P450 1a1 in human transitional carcinoma of the bladder Mol. Cancer Ther. 2011, 12, 27-37
    • (2011) Mol. Cancer Ther. , vol.12 , pp. 27-37
    • Sutherland, M.1    Gill, J.2    Loadman, P.M.3    Sheldrake, H.4    Searcey, M.5    Pors, K.6    Shnyder, S.D.7    Patterson, L.H.8
  • 17
    • 0043123409 scopus 로고    scopus 로고
    • Establishment of substituent effects in the DNA binding subunit of CBI analogues of the duocarmycins and CC-1065
    • Parrish, J. P.; Kastrinsky, D. B.; Stauffer, F.; Hedrick, M. P.; Hwang, I.; Boger, D. L. Establishment of substituent effects in the DNA binding subunit of CBI analogues of the duocarmycins and CC-1065 Bioorg. Med. Chem. 2003, 11, 3815-38
    • (2003) Bioorg. Med. Chem. , vol.11 , pp. 3815-3838
    • Parrish, J.P.1    Kastrinsky, D.B.2    Stauffer, F.3    Hedrick, M.P.4    Hwang, I.5    Boger, D.L.6
  • 19
    • 70949091047 scopus 로고    scopus 로고
    • Hypoxia-activated prodrugs: Substituent effects on the properties of nitro seco -1,2,9,9a-tetrahydrocyclopropa[ c ]-benz[ e ]indol-4-one (nitroCBI) prodrugs of DNA minor groove alkylating agents
    • Tercel, M.; Atwell, G. J.; Yang, S.; Stevenson, R.; Botting, K.; Smith, E.; Anderson, R. F.; Denny, W. A.; Wilson, W. R.; Pruijn, F. B. Hypoxia-activated prodrugs: substituent effects on the properties of nitro seco -1,2,9,9a-tetrahydrocyclopropa[ c ]-benz[ e ]indol-4-one (nitroCBI) prodrugs of DNA minor groove alkylating agents J. Med. Chem. 2009, 52, 7258-7272
    • (2009) J. Med. Chem. , vol.52 , pp. 7258-7272
    • Tercel, M.1    Atwell, G.J.2    Yang, S.3    Stevenson, R.4    Botting, K.5    Smith, E.6    Anderson, R.F.7    Denny, W.A.8    Wilson, W.R.9    Pruijn, F.B.10
  • 20
    • 33846209483 scopus 로고    scopus 로고
    • Tumour-specific expression of CYP2W1: Its potential as a drug target in cancer therapy
    • 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, 61-67
    • (2007) Expert Opin. Ther. Targets , vol.11 , pp. 61-67
    • Karlgren, M.1    Ingelman-Sundberg, M.2
  • 22
    • 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, B. S.; Tiong, K. H.; Muruhadas, A.; Randhawa, N.; Choo, H. L.; Bradshaw, T. D.; Stevens, M. F.; Leong, C. O. 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, 1982-1992
    • (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    Stevens, M.F.7    Leong, C.O.8
  • 23
    • 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, F. P. 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, 1740-1751
    • (2012) Chem. Res. Toxicol. , vol.25 , pp. 1740-1751
    • Wang, K.1    Guengerich, F.P.2
  • 24
    • 70350434097 scopus 로고    scopus 로고
    • Functional characterization of human cytochrome P450 2S1 using a synthetic gene-expressed protein in Escherichia coli
    • Bui, P. H.; Hankinson, O. Functional characterization of human cytochrome P450 2S1 using a synthetic gene-expressed protein in Escherichia coli Mol. Pharmacol. 2009, 76, 1031-1043
    • (2009) Mol. Pharmacol. , vol.76 , pp. 1031-1043
    • Bui, P.H.1    Hankinson, O.2
  • 25
    • 0030476592 scopus 로고    scopus 로고
    • Role of cytochrome P450 in oxazaphosphorine metabolism. Deactivation via N -dechloroethylation and activation via 4-hydroxylation catalyzed by distinct subsets of rat liver cytochromes P450
    • Yu, L.; Waxman, D. J. Role of cytochrome P450 in oxazaphosphorine metabolism. Deactivation via N -dechloroethylation and activation via 4-hydroxylation catalyzed by distinct subsets of rat liver cytochromes P450 Drug Metab. Dispos. 1996, 24, 1254-1262
    • (1996) Drug Metab. Dispos. , vol.24 , pp. 1254-1262
    • Yu, L.1    Waxman, D.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.