메뉴 건너뛰기




Volumn 42, Issue 25, 1999, Pages 5277-5283

Synthesis and biological evaluation of novel prodrugs of anthracyclines for selective activation by the tumor-associated protease plasmin

Author keywords

[No Author keywords available]

Indexed keywords

ANTHRACYCLINE DERIVATIVE; APROTININ; DAUNORUBICIN; DOXORUBICIN; PLASMIN; PRODRUG; UROKINASE;

EID: 0033576644     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm9910472     Document Type: Article
Times cited : (73)

References (30)
  • 1
    • 0030589728 scopus 로고    scopus 로고
    • A summary of monoclonal antibody-enzyme/prodrug
    • Senter, P. D.; Svensson, H. P. A summary of monoclonal antibody-enzyme/prodrug. Adv. Drug Deliv. Rev. 1996, 22, 341-349.
    • (1996) Adv. Drug Deliv. Rev. , vol.22 , pp. 341-349
    • Senter, P.D.1    Svensson, H.P.2
  • 2
    • 0012345936 scopus 로고
    • Radioimmunoconjugates: An overview of problems and promises
    • A limitation of the use of monoclonal antibodies is their slow extravasation. In human studies, it was found that only 0.001% of the injected dose of antibody commonly localizes to each gram of tumor. Sands, H. Radioimmunoconjugates: an overview of problems and promises. Antibody Immunoconjugates Radiopharm. 1988, 1, 213-226.
    • (1988) Antibody Immunoconjugates Radiopharm. , vol.1 , pp. 213-226
    • Sands, H.1
  • 5
    • 0001874589 scopus 로고
    • A novel one-step tumor selective prodrug activation system
    • Bosslet, K.; Czech, J.; Hoffman, D. A novel one-step tumor selective prodrug activation system. Tumor Targeting 1995, 1, 45-50.
    • (1995) Tumor Targeting , vol.1 , pp. 45-50
    • Bosslet, K.1    Czech, J.2    Hoffman, D.3
  • 7
    • 0011166658 scopus 로고
    • Anthracycline antibiotics. New analogues, methods of delivery, and mechanisms of action
    • American Chemical Society: Washington, DC
    • Priebe, W. Anthracycline Antibiotics. New analogues, methods of delivery, and mechanisms of action; ACS Symposium Series 574; American Chemical Society: Washington, DC, 1995.
    • (1995) ACS Symposium Series , vol.574
    • Priebe, W.1
  • 8
    • 0030896534 scopus 로고    scopus 로고
    • Cell biologic factors and cancer spread
    • Yamashita, Y.-I.; Ogawa, M. Cell biologic factors and cancer spread (review). Int. J. Oncol. 1997, 10, 807-813.
    • (1997) Int. J. Oncol. , vol.10 , pp. 807-813
    • Yamashita, Y.-I.1    Ogawa, M.2
  • 9
    • 0031733174 scopus 로고    scopus 로고
    • Multifunctional potential of the plasminogen activation system in tumor invasion and metastasis
    • Ruening, U.; Magdolen, V.; Wilhelm, O.; Fischer, K.; Lutz, V.; Graeff, H.; Schmitt, M. Multifunctional potential of the plasminogen activation system in tumor invasion and metastasis. Int. J. Oncol. 1998, 13, 893-906.
    • (1998) Int. J. Oncol. , vol.13 , pp. 893-906
    • Ruening, U.1    Magdolen, V.2    Wilhelm, O.3    Fischer, K.4    Lutz, V.5    Graeff, H.6    Schmitt, M.7
  • 10
    • 0030788411 scopus 로고    scopus 로고
    • The urokinase-type plasminogen activator system in cancer metastasis: A review
    • Andreasen, P. A.; Kjøller, L.; Christensen, L; Duffy, M. J. The urokinase-type plasminogen activator system in cancer metastasis: a review. Int. J. Cancer 1997, 72, 1-22.
    • (1997) Int. J. Cancer , vol.72 , pp. 1-22
    • Andreasen, P.A.1    Kjøller, L.2    Christensen, L.3    Duffy, M.J.4
  • 11
    • 0030339567 scopus 로고    scopus 로고
    • The biochemistry of metastasis
    • Duffy, M. J. The biochemistry of metastasis. Adv. Clin. Chem. 1996, 32, 136-166.
    • (1996) Adv. Clin. Chem. , vol.32 , pp. 136-166
    • Duffy, M.J.1
  • 12
    • 0026046509 scopus 로고
    • Metastatic behaviour of human melanoma cell lines in nude mice correlates with urokinase-type plasminogen activator, its type I inhibitor, and urokinase-mediated matrix degradation
    • Quax, P. H. A.; Van Muijen, G. N. P.; Weening-Verhoeff, E. J. D.; Lund, L. R.; Danø, K.; Ruiter, D. J.; Verheijen, J. H. Metastatic behaviour of human melanoma cell lines in nude mice correlates with urokinase-type plasminogen activator, its type I inhibitor, and urokinase-mediated matrix degradation. Cell Biol. 1991, 115, 191-199.
    • (1991) Cell Biol. , vol.115 , pp. 191-199
    • Quax, P.H.A.1    Van Muijen, G.N.P.2    Weening-Verhoeff, E.J.D.3    Lund, L.R.4    Danø, K.5    Ruiter, D.J.6    Verheijen, J.H.7
  • 13
    • 0030838465 scopus 로고    scopus 로고
    • The plasminogen activator and matrix metalloproteinase production and extracellular matrix degradation by rat prostate cancer cells in vitro: Correlation with metastatic behaviour in vivo
    • Quax, P. H. A.; de Bart, A. C. W.; Schalken, J. A.; Verheijen, J. H. The plasminogen activator and matrix metalloproteinase production and extracellular matrix degradation by rat prostate cancer cells in vitro: correlation with metastatic behaviour in vivo. Prostate 1997, 32, 196-204.
    • (1997) Prostate , vol.32 , pp. 196-204
    • Quax, P.H.A.1    De Bart, A.C.W.2    Schalken, J.A.3    Verheijen, J.H.4
  • 15
    • 0029894671 scopus 로고    scopus 로고
    • Stromal cell expression of components of matrix-degrading protease systems in human cancer
    • Hewitt, R.; Danø, K.; Stromal cell expression of components of matrix-degrading protease systems in human cancer. Enzyme Protein 1996, 49, 163-173.
    • (1996) Enzyme Protein , vol.49 , pp. 163-173
    • Hewitt, R.1    Danø, K.2
  • 16
    • 0025307952 scopus 로고
    • Protein and messenger RNA levels of plasminogen activators and inhibitors analyzed in 22 human tumor cell lines
    • Quax, P. H. A.; van Leeuwen, R. T. J.; Verspaget H. W.; Verheijen, J. H. Protein and messenger RNA levels of plasminogen activators and inhibitors analyzed in 22 human tumor cell lines. Cancer Res. 1990, 50, 1488-1494.
    • (1990) Cancer Res. , vol.50 , pp. 1488-1494
    • Quax, P.H.A.1    Van Leeuwen, R.T.J.2    Verspaget, H.W.3    Verheijen, J.H.4
  • 21
    • 0020644940 scopus 로고
    • Plasmin-activated prodrugs for cancer chemotherapy. 2. Synthesis and biological activity of peptidyl derivatives of doxorubicin
    • Chakravarty, P. K.; Carl, P. L.; Weber, M. J.; Katzenellenbogen, J. A. Plasmin-activated prodrugs for cancer chemotherapy. 2. Synthesis and biological activity of peptidyl derivatives of doxorubicin. J. Med. Chem. 1983, 26, 638-644.
    • (1983) J. Med. Chem. , vol.26 , pp. 638-644
    • Chakravarty, P.K.1    Carl, P.L.2    Weber, M.J.3    Katzenellenbogen, J.A.4
  • 23
    • 0000315290 scopus 로고
    • Reduction of anticancer drug toxicity. Pharmacologic, biologic, immunologic and gene therapeutic approaches
    • Zeller, W. J., Eisenbrand, G., Hellmann, K., Eds.
    • Lauck-Birkel, S.; Tang, W. C.; Wagner, B.; Fiebig, H. H.; Kohlmüller, D.; Eisenbrand, G. In Reduction of anticancer drug toxicity. Pharmacologic, biologic, immunologic and gene therapeutic approaches; Zeller, W. J., Eisenbrand, G., Hellmann, K., Eds.; Contrib. Oncol. 1995, 48, 189-194.
    • (1995) Contrib. Oncol. , vol.48 , pp. 189-194
    • Lauck-Birkel, S.1    Tang, W.C.2    Wagner, B.3    Fiebig, H.H.4    Kohlmüller, D.5    Eisenbrand, G.6
  • 24
    • 0029839133 scopus 로고    scopus 로고
    • An approach towards more selective anticancer agents
    • Eisenbrand, G.; Lauck-Birkel, S.; Tang, W. C. An approach towards more selective anticancer agents. Synthesis 1996, 1246-1258.
    • (1996) Synthesis , pp. 1246-1258
    • Eisenbrand, G.1    Lauck-Birkel, S.2    Tang, W.C.3
  • 25
    • 0030792535 scopus 로고    scopus 로고
    • Monomethoxytrityl (MMT) as a versatile amino protecting group for complex prodrugs of anticancer compounds sensitive to strong acids, bases and nucleophiles
    • Dubowchik, G. M.; Radia S. Monomethoxytrityl (MMT) as a versatile amino protecting group for complex prodrugs of anticancer compounds sensitive to strong acids, bases and nucleophiles. Tetrahedron Lett. 1997, 38, 5257-5260.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 5257-5260
    • Dubowchik, G.M.1    Radia, S.2
  • 26
    • 0032402354 scopus 로고    scopus 로고
    • Cathepsin B-sensitive dipeptide prodrugs. 1. A model study of structural requirements for efficient release of doxorubicin
    • Dubowchik, G. M.; Firestone, R. A. Cathepsin B-sensitive dipeptide prodrugs. 1. A model study of structural requirements for efficient release of doxorubicin. Bioorg. Med. Chem. Lett. 1998, 8, 3341-3346.
    • (1998) Bioorg. Med. Chem. Lett. , vol.8 , pp. 3341-3346
    • Dubowchik, G.M.1    Firestone, R.A.2
  • 27
    • 0032402572 scopus 로고    scopus 로고
    • Cathepsin B-sensitive dipeptide prodrugs. 2. Models of anticancer drugs paclitaxel (Taxol), mytomycin c and doxorubicin
    • Dubowchik, G. M.; Mosure, K.; Knipe, J. O.; Firestone, R. A. Cathepsin B-sensitive dipeptide prodrugs. 2. Models of anticancer drugs paclitaxel (Taxol), mytomycin c and doxorubicin. Bioorg. Med. Chem. Lett. 1998, 8, 3347-3352.
    • (1998) Bioorg. Med. Chem. Lett. , vol.8 , pp. 3347-3352
    • Dubowchik, G.M.1    Mosure, K.2    Knipe, J.O.3    Firestone, R.A.4
  • 29
    • 0342452717 scopus 로고    scopus 로고
    • Cell lines: MCF-7, breast cancer; EVSA-T, breast cancer; WIDR, colon cancer; IGROV, ovarian cancer; M19, melanoma; A498, renal cancer; H226, nonsmall cell lung cancer
    • Cell lines: MCF-7, breast cancer; EVSA-T, breast cancer; WIDR, colon cancer; IGROV, ovarian cancer; M19, melanoma; A498, renal cancer; H226, nonsmall cell lung cancer.
  • 30
    • 0025878872 scopus 로고
    • Comparison of the sulforhodamine B protein and tetrazolium (MTT) assays for in vitro chemosensitivity testing
    • Kepers, Y. P.; Peters, G. J.; van Ark-Otte, J.; Winograd, B.; Pinedo, H. M.; Comparison of the sulforhodamine B protein and tetrazolium (MTT) assays for in vitro chemosensitivity testing. Eur. J. Cancer 1991, 27, 897-900.
    • (1991) Eur. J. Cancer , vol.27 , pp. 897-900
    • Kepers, Y.P.1    Peters, G.J.2    Van Ark-Otte, J.3    Winograd, B.4    Pinedo, H.M.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.