메뉴 건너뛰기




Volumn 50, Issue 4, 1998, Pages 387-394

The design of selectively-activated anti-cancer prodrugs for use in antibody-directed and gene-directed enzyme-prodrug therapies

Author keywords

[No Author keywords available]

Indexed keywords

5 (1 AZIRIDINYL) 2,4 DINITROBENZAMIDE; ANILINE MUSTARD DERIVATIVE; ANTINEOPLASTIC AGENT; ANTINEOPLASTIC ANTIBIOTIC; BETA GLUCURONIDASE; BETA LACTAMASE; CARBOXYPEPTIDASE; CARZELESIN; CYCLOPHOSPHAMIDE; CYTOSINE DEAMINASE; CYTOTOXIN; DEACETYLVINBLASTINE; DUOCARMYCIN A; ENZYME; EPIRUBICIN; FLUCYTOSINE; GANCICLOVIR; MONOCLONAL ANTIBODY; PRODRUG; SN 23862; THYMIDINE KINASE; TUMOR PROTEIN; UNCLASSIFIED DRUG;

EID: 0031956262     PISSN: 00223573     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.2042-7158.1998.tb06878.x     Document Type: Conference Paper
Times cited : (67)

References (50)
  • 1
    • 0028722685 scopus 로고
    • Conjugates of COL-1 monoclonal antibody and beta-D-galactosidase can specifically kill tumor cells by generation of 5-fluorouridine from the prodrug beta-D-galactosyl-5-fluorouridine
    • Abraham, R., Aman, N., von Borstel, R., Darsley, M., Kamireddy, B., Renten, J., Morris, G., Titmas, R. (1994) Conjugates of COL-1 monoclonal antibody and beta-D-galactosidase can specifically kill tumor cells by generation of 5-fluorouridine from the prodrug beta-D-galactosyl-5-fluorouridine. Cell Biophys. 24/25: 127-133
    • (1994) Cell Biophys. , vol.24-25 , pp. 127-133
    • Abraham, R.1    Aman, N.2    Von Borstel, R.3    Darsley, M.4    Kamireddy, B.5    Renten, J.6    Morris, G.7    Titmas, R.8
  • 2
    • 0026745562 scopus 로고
    • The bioactivation of 5-(aziridin-1-yl)-2,4-dinitrobenzamide (CB1954) I. Purification and properties of a nitroreductase enzyme from Escherichia coli - A potential enzyme for antibody-directed enzyme prodrug therapy (ADEPT)
    • Anlezark, G. M., Melton, R. G., Sherwood, R. F., Coles, B., Friedlos, F., Knox, R. J. (1992) The bioactivation of 5-(aziridin-1-yl)-2,4-dinitrobenzamide (CB1954) I. Purification and properties of a nitroreductase enzyme from Escherichia coli - a potential enzyme for antibody-directed enzyme prodrug therapy (ADEPT). Biochem. Pharmacol. 44: 2289-2295
    • (1992) Biochem. Pharmacol. , vol.44 , pp. 2289-2295
    • Anlezark, G.M.1    Melton, R.G.2    Sherwood, R.F.3    Coles, B.4    Friedlos, F.5    Knox, R.J.6
  • 4
    • 0030916634 scopus 로고    scopus 로고
    • Synthesis and cytotoxicity of amino analogues of the potent DNA alkylating agent seco-CBI-TMI
    • Atwell, G. J., Wilson, W. R., Denny, W. A. (1997) Synthesis and cytotoxicity of amino analogues of the potent DNA alkylating agent seco-CBI-TMI. Bioorg. Med. Chem. Lett. 7: 1493-1496
    • (1997) Bioorg. Med. Chem. Lett. , vol.7 , pp. 1493-1496
    • Atwell, G.J.1    Wilson, W.R.2    Denny, W.A.3
  • 5
    • 0028592664 scopus 로고
    • Antibody-directed enzyme-prodrug therapy (ADEPT): A review of some theoretical, experimental and clinical aspects
    • Bagshawe, K. D., Sharma, S. K., Springer, C. J., Rogers, G. T. (1994) Antibody-directed enzyme-prodrug therapy (ADEPT): a review of some theoretical, experimental and clinical aspects. Ann. Oncol. 5: 879-891
    • (1994) Ann. Oncol. , vol.5 , pp. 879-891
    • Bagshawe, K.D.1    Sharma, S.K.2    Springer, C.J.3    Rogers, G.T.4
  • 7
    • 0025143478 scopus 로고
    • Synthesis and preliminary evaluation of agents incorporating the pharmacophore of the duocarmycin/pyrindamycin alkylation subunit: Identification of the CC-1065/duocarmycin common pharmacophore
    • Boger, D. L., Ishizaki, T., Zarrinmayeh, H., Kitos, P. A., Suntornwat, O. (1990) Synthesis and preliminary evaluation of agents incorporating the pharmacophore of the duocarmycin/pyrindamycin alkylation subunit: identification of the CC-1065/duocarmycin common pharmacophore. J. Org. Chem. 55: 4499-4502
    • (1990) J. Org. Chem. , vol.55 , pp. 4499-4502
    • Boger, D.L.1    Ishizaki, T.2    Zarrinmayeh, H.3    Kitos, P.A.4    Suntornwat, O.5
  • 8
    • 0029782488 scopus 로고    scopus 로고
    • CC-1065 and the duocarmycins: Understanding their biological function through mechanistic studies
    • Boger, D. L., Johnson, D. S. (1996) CC-1065 and the duocarmycins: understanding their biological function through mechanistic studies. Angew. Chem. Int. Ed. Engl. 35: 1438-1474
    • (1996) Angew. Chem. Int. Ed. Engl. , vol.35 , pp. 1438-1474
    • Boger, D.L.1    Johnson, D.S.2
  • 9
    • 0026034848 scopus 로고
    • The differences in kinetics of rat and human DT diaphorase result in a differential sensitivity of derived cells lines to CB1954 (5-(aziridin-1-yl)-2,4-dinitrobenzamide)
    • Boland, M. P., Knox, R. J., Roberts, J. J. (1991) The differences in kinetics of rat and human DT diaphorase result in a differential sensitivity of derived cells lines to CB1954 (5-(aziridin-1-yl)-2,4-dinitrobenzamide). Biochem. Pharmacol. 41: 867-875
    • (1991) Biochem. Pharmacol. , vol.41 , pp. 867-875
    • Boland, M.P.1    Knox, R.J.2    Roberts, J.J.3
  • 10
    • 0030956976 scopus 로고    scopus 로고
    • The bystander effect of the nitroreductase CB 1954 enzyme prodrug system is due to a cell-permeable metabolite
    • Bridgewater, J. A., Knox, R. J., Pitts, J. D., Collins, M. K., Springer, C. J. (1997) The bystander effect of the nitroreductase CB 1954 enzyme prodrug system is due to a cell-permeable metabolite. Human Gene Ther. 8: 709-717
    • (1997) Human Gene Ther. , vol.8 , pp. 709-717
    • Bridgewater, J.A.1    Knox, R.J.2    Pitts, J.D.3    Collins, M.K.4    Springer, C.J.5
  • 11
    • 0014525030 scopus 로고
    • 2,4-Dinitro-5-ethyleneiminobenzamide (CB1954): A potent and selective inhibitor of the growth of the Walker carcinoma 256
    • Cobb, L. M., Connors, T. A., Elson, L. A., Khan, A. H., Mitchley, B. V. C., Ross, W. J. C., Whisson, M. E. (1969) 2,4-Dinitro-5-ethyleneiminobenzamide (CB1954): a potent and selective inhibitor of the growth of the Walker carcinoma 256. Biochem. Pharmacol. 8: 1519-1527
    • (1969) Biochem. Pharmacol. , vol.8 , pp. 1519-1527
    • Cobb, L.M.1    Connors, T.A.2    Elson, L.A.3    Khan, A.H.4    Mitchley, B.V.C.5    Ross, W.J.C.6    Whisson, M.E.7
  • 12
    • 0023910405 scopus 로고
    • Hypoxia in tumors: A paradigm for the approach to biochemical and physiological heterogeneity
    • Coleman, C. N. (1988). Hypoxia in tumors: a paradigm for the approach to biochemical and physiological heterogeneity. J. Natl Cancer Inst. 80: 310-317
    • (1988) J. Natl Cancer Inst. , vol.80 , pp. 310-317
    • Coleman, C.N.1
  • 13
    • 0029922596 scopus 로고    scopus 로고
    • Multicellular membranes as an in vitro model for extravascular diffusion in tumours
    • Cowan, D. S. M., Hicks, K. O., Wilson, W. R. (1996) Multicellular membranes as an in vitro model for extravascular diffusion in tumours. Br. J. Cancer 74 (Suppl. XXVII): 28-31
    • (1996) Br. J. Cancer , vol.74 , Issue.27 SUPPL. , pp. 28-31
    • Cowan, D.S.M.1    Hicks, K.O.2    Wilson, W.R.3
  • 14
    • 0030476553 scopus 로고    scopus 로고
    • Gene therapy for malignant neoplasms of the CNS
    • Culver, K. W. (1996) Gene therapy for malignant neoplasms of the CNS (Review). Bone Marrow Transpl. 18 (Suppl. 3): S6-S9
    • (1996) Bone Marrow Transpl. , vol.18 , Issue.3 SUPPL.
    • Culver, K.W.1
  • 15
    • 0001687859 scopus 로고    scopus 로고
    • The design of selectively-activated prodrugs for cancer chemotherapy
    • Denny, W. A. (1996) The design of selectively-activated prodrugs for cancer chemotherapy. Curr. Pharm. Design 2: 281-294
    • (1996) Curr. Pharm. Design , vol.2 , pp. 281-294
    • Denny, W.A.1
  • 16
    • 0027219332 scopus 로고
    • Bioreducible mustards: A paradigm for hypoxia-selective prodrugs of diffusible cytotoxins (HPDCs)
    • Denny, W. A., Wilson, W. R. (1993) Bioreducible mustards: a paradigm for hypoxia-selective prodrugs of diffusible cytotoxins (HPDCs). Cancer Met. Rev. 12: 135-151
    • (1993) Cancer Met. Rev. , vol.12 , pp. 135-151
    • Denny, W.A.1    Wilson, W.R.2
  • 17
    • 0029884764 scopus 로고    scopus 로고
    • Recent developments in the design of bioreductive drugs
    • Denny, W. A., Wilson, W. R., Hay, M. P. (1996) Recent developments in the design of bioreductive drugs. Br. J. Cancer 74 (Suppl. XXVII): 32-38
    • (1996) Br. J. Cancer , vol.74 , Issue.27 SUPPL. , pp. 32-38
    • Denny, W.A.1    Wilson, W.R.2    Hay, M.P.3
  • 20
    • 7144244481 scopus 로고    scopus 로고
    • Reaction of 6-amino analogues of the duocarmycin series with DNA; isolation and identification of the major adduct
    • in press
    • Fan, J.-Y., Tercel, M., Tan, L. K., Boyd, M., Denny, W. A. (1998) Reaction of 6-amino analogues of the duocarmycin series with DNA; isolation and identification of the major adduct. Chem. Res. Tox., in press
    • (1998) Chem. Res. Tox.
    • Fan, J.-Y.1    Tercel, M.2    Tan, L.K.3    Boyd, M.4    Denny, W.A.5
  • 21
    • 0029917028 scopus 로고    scopus 로고
    • Reductase enzyme expression across the National Cancer Institute Tumor cell line panel: Correlation with sensitivity to mitomycin C and EO9
    • Fitzsimmons, S. A., Workman, P., Grever, M., Paull, K., Camalier, R., Lewis, A. D. (1996) Reductase enzyme expression across the National Cancer Institute Tumor cell line panel: correlation with sensitivity to mitomycin C and EO9. J. Natl Cancer Inst. 88: 259-269
    • (1996) J. Natl Cancer Inst. , vol.88 , pp. 259-269
    • Fitzsimmons, S.A.1    Workman, P.2    Grever, M.3    Paull, K.4    Camalier, R.5    Lewis, A.D.6
  • 22
    • 0030907756 scopus 로고    scopus 로고
    • Structure-activity relationships for activation of dinitrophenylcarboxamide mustards by E. coli nitroreductase in GDEPT (gene-directed enzyme prodrug therapy)
    • Friedlos, F., Denny, W. A., Palmer, B. D., Springer, C. J. (1997) Structure-activity relationships for activation of dinitrophenylcarboxamide mustards by E. coli nitroreductase in GDEPT (gene-directed enzyme prodrug therapy). J. Med. Chem. 40: 1270-1275
    • (1997) J. Med. Chem. , vol.40 , pp. 1270-1275
    • Friedlos, F.1    Denny, W.A.2    Palmer, B.D.3    Springer, C.J.4
  • 24
    • 0026802983 scopus 로고
    • A monoclonal antibody-β-glucuronidase conjugate as activator of the prodrug epirubicin-glucuronide for the specific treatment of cancer
    • Haisma, H. J., Boven, E., van Muijen, M., de Jong, J., van der Vijgh, W. J., Pinedo, H. M. (1992) A monoclonal antibody-β-glucuronidase conjugate as activator of the prodrug epirubicin-glucuronide for the specific treatment of cancer. Br. J. Cancer 66: 474-478
    • (1992) Br. J. Cancer , vol.66 , pp. 474-478
    • Haisma, H.J.1    Boven, E.2    Van Muijen, M.3    De Jong, J.4    Van Der Vijgh, W.J.5    Pinedo, H.M.6
  • 25
    • 0029803995 scopus 로고    scopus 로고
    • Antibody-directed enzyme-prodrug therapy (ADEPT)
    • Hay, M. P., Denny, W. A. (1996) Antibody-directed enzyme-prodrug therapy (ADEPT). Drugs Future 21: 917-931
    • (1996) Drugs Future , vol.21 , pp. 917-931
    • Hay, M.P.1    Denny, W.A.2
  • 26
    • 0028793511 scopus 로고
    • A novel enediyne prodrug for antibody-directed enzyme prodrug therapy (ADEPT) using E. coli B nitroreductase
    • Hay, M. P., Wilson, W. R., Denny, W. A. (1995) A novel enediyne prodrug for antibody-directed enzyme prodrug therapy (ADEPT) using E. coli B nitroreductase. Bioorg. Med. Chem. Lett. 5: 2829-2834
    • (1995) Bioorg. Med. Chem. Lett. , vol.5 , pp. 2829-2834
    • Hay, M.P.1    Wilson, W.R.2    Denny, W.A.3
  • 27
    • 0030866977 scopus 로고    scopus 로고
    • An experimental and mathematical model for the extravascular treatment of a DNA intercalator in tumours
    • Hicks, K. O., Ohms, S. J., van Zilj, P., Denny, W. A., Hunter, P. J., Wilson, W. R. (1997) An experimental and mathematical model for the extravascular treatment of a DNA intercalator in tumours. Br. J. Cancer. 76: 894-903
    • (1997) Br. J. Cancer. , vol.76 , pp. 894-903
    • Hicks, K.O.1    Ohms, S.J.2    Van Zilj, P.3    Denny, W.A.4    Hunter, P.J.5    Wilson, W.R.6
  • 28
  • 30
    • 0026075733 scopus 로고
    • Bioactivation of CB 1954: Reaction of the active 4-hydroxylamino derivative with thioesters to form the ultimate DNA-DNA interstrand cross-linking species
    • Knox, R. J., Friedlos, F., Marchbank, T., Roberts, J. J. (1991) Bioactivation of CB 1954: reaction of the active 4-hydroxylamino derivative with thioesters to form the ultimate DNA-DNA interstrand cross-linking species. Biochem. Pharmacol. 42: 1691-1697
    • (1991) Biochem. Pharmacol. , vol.42 , pp. 1691-1697
    • Knox, R.J.1    Friedlos, F.2    Marchbank, T.3    Roberts, J.J.4
  • 31
    • 0029009389 scopus 로고
    • Virtual cofactors for an Escherichia coli nitroreductase enzyme-relevance to reductively activated prodrugs in antibody-directed enzyme prodrug therapy (ADEPT)
    • Knox, R. J., Friedlos, F., Jarman, M., Davies, L. C., Goddard, P., Anlezark, G. M., Melton, R. G., Sherwood, R. F. (1995) Virtual cofactors for an Escherichia coli nitroreductase enzyme-relevance to reductively activated prodrugs in antibody-directed enzyme prodrug therapy (ADEPT). Biochem. Pharmacol. 49: 1641-1647
    • (1995) Biochem. Pharmacol. , vol.49 , pp. 1641-1647
    • Knox, R.J.1    Friedlos, F.2    Jarman, M.3    Davies, L.C.4    Goddard, P.5    Anlezark, G.M.6    Melton, R.G.7    Sherwood, R.F.8
  • 33
    • 0031087212 scopus 로고    scopus 로고
    • Enzyme/prodrug gene therapy approach for breast cancer using a recombinant adenovirus expressing Escherichia coli cytosine deaminase
    • Li, Z., Shanmugam, N., Katayose, D., Huber, B., Srivastava, S., Cowan, K., Seth, P. (1997) Enzyme/prodrug gene therapy approach for breast cancer using a recombinant adenovirus expressing Escherichia coli cytosine deaminase. Cancer Gene Ther. 4: 113-117
    • (1997) Cancer Gene Ther. , vol.4 , pp. 113-117
    • Li, Z.1    Shanmugam, N.2    Katayose, D.3    Huber, B.4    Srivastava, S.5    Cowan, K.6    Seth, P.7
  • 34
    • 0028090161 scopus 로고
    • Self-immolative prodrugs: Candidates for antibody-directed enzyme prodrug therapy in conjunction with a nitroreductase enzyme
    • Mauger, A. B., Burke, P. J., Somani, H. H., Friedlos, F., Knox, R. J. (1994) Self-immolative prodrugs: candidates for antibody-directed enzyme prodrug therapy in conjunction with a nitroreductase enzyme. J. Med. Chem. 37: 3452-3458
    • (1994) J. Med. Chem. , vol.37 , pp. 3452-3458
    • Mauger, A.B.1    Burke, P.J.2    Somani, H.H.3    Friedlos, F.4    Knox, R.J.5
  • 35
    • 0026487592 scopus 로고
    • Preparation and characterization of a beta-lactamase-Fab′ conjugate for the site-specific activation of oncolytic agents
    • Meyer, M. L., Jungheim, L. N., Mikolajczyk, S. D., Shepherd, T. A., Starling, J. J., Ahlem, C. N. (1992) Preparation and characterization of a beta-lactamase-Fab′ conjugate for the site-specific activation of oncolytic agents. Bioconjug. Chem. 3: 42-48
    • (1992) Bioconjug. Chem. , vol.3 , pp. 42-48
    • Meyer, M.L.1    Jungheim, L.N.2    Mikolajczyk, S.D.3    Shepherd, T.A.4    Starling, J.J.5    Ahlem, C.N.6
  • 36
    • 0027220125 scopus 로고
    • Site-specific prodrug activation by antibody-β-lactamase conjugates: Regression and long-term growth inhibition of human colon carcinoma xenograft models
    • Meyer, M. L., Jungheim, L. N., Law, K. L., Mikolajczyk, S. D., Shepherd, T. A., Mackensen, D. G., Briggs, S. L., Starling, J. J. (1993) Site-specific prodrug activation by antibody-β-lactamase conjugates: regression and long-term growth inhibition of human colon carcinoma xenograft models. Cancer Res. 53: 3956-3963
    • (1993) Cancer Res. , vol.53 , pp. 3956-3963
    • Meyer, M.L.1    Jungheim, L.N.2    Law, K.L.3    Mikolajczyk, S.D.4    Shepherd, T.A.5    Mackensen, D.G.6    Briggs, S.L.7    Starling, J.J.8
  • 37
    • 0026718016 scopus 로고
    • Designed enediynes: A new class of DNA-cleaving molecules with potent and selective anticancer activity
    • Nicolaou, K. C., Dai, W.-M., Tsay, S.-C., Estevez, V. A., Wrasidlo, W. (1992) Designed enediynes: a new class of DNA-cleaving molecules with potent and selective anticancer activity. Science 256: 1172-1178
    • (1992) Science , vol.256 , pp. 1172-1178
    • Nicolaou, K.C.1    Dai, W.-M.2    Tsay, S.-C.3    Estevez, V.A.4    Wrasidlo, W.5
  • 38
    • 0027319406 scopus 로고
    • Chemistry and biology of natural and designed enediynes
    • Nicolaou, K. C., Smith, A. L., Yue, E. W. (1993) Chemistry and biology of natural and designed enediynes. Proc. Natl Acad. Sci. USA 90: 5881-5888
    • (1993) Proc. Natl Acad. Sci. USA , vol.90 , pp. 5881-5888
    • Nicolaou, K.C.1    Smith, A.L.2    Yue, E.W.3
  • 39
    • 0030016605 scopus 로고    scopus 로고
    • A randomized phase II study with two schedules of the novel indoloquinone EO9 in non-small-cell lung cancer: A study of the EORTC Early Clinical Studies Group (ECSG)
    • Pavlidis, N., Hanauske, A. R., Gamucci, T., Smyth, J., Lehnert, M., te Velde, A., Lan, J., Verweij, J. (1996) A randomized phase II study with two schedules of the novel indoloquinone EO9 in non-small-cell lung cancer: a study of the EORTC Early Clinical Studies Group (ECSG). Ann. Oncol. 7: 529-531
    • (1996) Ann. Oncol. , vol.7 , pp. 529-531
    • Pavlidis, N.1    Hanauske, A.R.2    Gamucci, T.3    Smyth, J.4    Lehnert, M.5    Te Velde, A.6    Lan, J.7    Verweij, J.8
  • 40
    • 0028984807 scopus 로고
    • Transcriptional regulatory sequences of carcinoembryonic antigen: Identification and use with cytosine deaminase for tumor-specific gene therapy
    • Richards, C. A., Austin, E. A., Huber, B. E. (1995) Transcriptional regulatory sequences of carcinoembryonic antigen: identification and use with cytosine deaminase for tumor-specific gene therapy. Human Gene Ther. 6: 881-893
    • (1995) Human Gene Ther. , vol.6 , pp. 881-893
    • Richards, C.A.1    Austin, E.A.2    Huber, B.E.3
  • 41
    • 0031306972 scopus 로고    scopus 로고
    • Nitro reduction as an electronic switch for bioreductive drug activation
    • Siim, B. G., Denny, W. A., Wilson, W. R. (1997) Nitro reduction as an electronic switch for bioreductive drug activation. Oncol. Res. 9: 357-369
    • (1997) Oncol. Res. , vol.9 , pp. 357-369
    • Siim, B.G.1    Denny, W.A.2    Wilson, W.R.3
  • 42
    • 0029621825 scopus 로고
    • Optimization of alkylating agent prodrugs derived from phenol and aniline mustards: A new clinical candidate prodrug (ZD2767) for antibody-directed enzyme-prodrug therapy (ADEPT)
    • Springer, C. J., Dowell, R., Burke, P. J., Hadley, E., Davies, D. H., Blakey, D. C., Melton, R. J., Niculescu-Duvaz, I. (1995) Optimization of alkylating agent prodrugs derived from phenol and aniline mustards: a new clinical candidate prodrug (ZD2767) for antibody-directed enzyme-prodrug therapy (ADEPT). J. Med. Chem. 38: 5051-5065
    • (1995) J. Med. Chem. , vol.38 , pp. 5051-5065
    • Springer, C.J.1    Dowell, R.2    Burke, P.J.3    Hadley, E.4    Davies, D.H.5    Blakey, D.C.6    Melton, R.J.7    Niculescu-Duvaz, I.8
  • 43
    • 0024379967 scopus 로고
    • Acid pH in tumors and its potential for therapeutic exploitation
    • Tannock, I. F., Rotin, D. (1989) Acid pH in tumors and its potential for therapeutic exploitation. Cancer Res. 49: 4373-4384
    • (1989) Cancer Res. , vol.49 , pp. 4373-4384
    • Tannock, I.F.1    Rotin, D.2
  • 44
    • 0030593869 scopus 로고    scopus 로고
    • Nitrogen and sulfur analogues of the seco-CI alkylating agent: Synthesis and cytotoxicity
    • Tercel, M., Denny, W. A., Wilson, W. R. (1996a) Nitrogen and sulfur analogues of the seco-CI alkylating agent: synthesis and cytotoxicity. Bioorg. Med. Chem. Lett. 6: 2735-2740
    • (1996) Bioorg. Med. Chem. Lett. , vol.6 , pp. 2735-2740
    • Tercel, M.1    Denny, W.A.2    Wilson, W.R.3
  • 45
    • 0030593879 scopus 로고    scopus 로고
    • A novel nitro-substituted seco-CI: Application as a reductively activated ADEPT prodrug
    • Tercel, M., Denny, W. A., Wilson, W. R. (1996b) A novel nitro-substituted seco-CI: application as a reductively activated ADEPT prodrug. Bioorg. Med. Chem. Lett. 6: 2741-2744
    • (1996) Bioorg. Med. Chem. Lett. , vol.6 , pp. 2741-2744
    • Tercel, M.1    Denny, W.A.2    Wilson, W.R.3
  • 46
    • 0024334082 scopus 로고
    • Proton-mediated liberation of aldophosphamide from a non-toxic prodrug: A strategy for tumor-selective activation of cytocidal drugs
    • Tietze, L. F., Newman, M., Mollers, T., Fischer, R., Glusenkamp, K.-H., Rajewsky, M., Jahde, E. (1989) Proton-mediated liberation of aldophosphamide from a non-toxic prodrug: a strategy for tumor-selective activation of cytocidal drugs. Cancer Res. 49: 4179-4184
    • (1989) Cancer Res. , vol.49 , pp. 4179-4184
    • Tietze, L.F.1    Newman, M.2    Mollers, T.3    Fischer, R.4    Glusenkamp, K.-H.5    Rajewsky, M.6    Jahde, E.7
  • 47
    • 0026794283 scopus 로고
    • Specific activation of glucuronide prodrugs by antibody-targeted enzyme conjugates for cancer therapy
    • Wang, S.-M., Chern, J.-W., Yeh, M.-Y., Ng, J. C., Tung, E., Roffler, S. R. (1992) Specific activation of glucuronide prodrugs by antibody-targeted enzyme conjugates for cancer therapy. Cancer Res. 52: 4484-4491
    • (1992) Cancer Res. , vol.52 , pp. 4484-4491
    • Wang, S.-M.1    Chern, J.-W.2    Yeh, M.-Y.3    Ng, J.C.4    Tung, E.5    Roffler, S.R.6
  • 48
    • 0010313514 scopus 로고
    • Tumour hypoxia: Challenges for cancer chemotherapy
    • Waring, M. J., Ponder, B. A. J. (eds) Chapter 4, Kluwer, Lancaster
    • Wilson, W. R. (1992) Tumour hypoxia: challenges for cancer chemotherapy. In: Waring, M. J., Ponder, B. A. J. (eds) Cancer Biology and Medicine. Volume 3: The Search for Anti-Cancer Drugs, Chapter 4, Kluwer, Lancaster
    • (1992) Cancer Biology and Medicine. Volume 3: The Search for Anti-Cancer Drugs , vol.3
    • Wilson, W.R.1
  • 49
    • 0003145062 scopus 로고    scopus 로고
    • Radiation-activated cytotoxins: A new use for Roentgen's rays in cancer treatment
    • Hagen, U., Harder, D., Jung, H., Streffer, C. (eds)
    • Wilson, W. R., Denny, W. A., Tercel, M. (1996) Radiation-activated cytotoxins: a new use for Roentgen's rays in cancer treatment. In: Hagen, U., Harder, D., Jung, H., Streffer, C. (eds) Proc. 10th Int. Congr. Radiat. Res. Vol. 2, pp 791-794
    • (1996) Proc. 10th Int. Congr. Radiat. Res. , vol.2 , pp. 791-794
    • Wilson, W.R.1    Denny, W.A.2    Tercel, M.3
  • 50
    • 0029803727 scopus 로고    scopus 로고
    • Vectors for cancer gene therapy
    • Zhang, J., Russell, S. J. (1996) Vectors for cancer gene therapy. Cancer Met. Rev. 15: 385-401
    • (1996) Cancer Met. Rev. , vol.15 , pp. 385-401
    • Zhang, J.1    Russell, S.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.