메뉴 건너뛰기




Volumn 10, Issue 9, 2004, Pages 3156-3168

Decreased Nucleotide Excision Repair Activity and Alterations of Topoisomerase IIα Are Associated with the in Vivo Resistance of a P388 Leukemia Subline to F11782, a Novel Catalytic Inhibitor of Topoisomerases I and II

Author keywords

[No Author keywords available]

Indexed keywords

2,3 BIS(3,5 DIOXO 1 PIPERAZINYL)BUTANE; 6 [2 (DIMETHYLAMINO)ETHYLAMINO] 3 HYDROXY 7H INDENO[2,1 C]QUINOLIN 7 ONE; CAMPTOTHECIN; CARMUSTINE; CISPLATIN; COLCHICINE; CYCLOPHOSPHAMIDE; DNA TOPOISOMERASE (ATP HYDROLYSING); DNA TOPOISOMERASE INHIBITOR; DOXORUBICIN; ENDONUCLEASE; ETOPOFOS; F 11782; FLUOROURACIL; GLUTATHIONE; GYRASE INHIBITOR; IRINOTECAN; MERBARONE; MESSENGER RNA; METHOTREXATE; MITOXANTRONE; NAVELBINE; PROTEIN XPG; TAFLUPOSIDE; TENIPOSIDE; TOPOTECAN; UNCLASSIFIED DRUG; VINBLASTINE; VINCA ALKALOID; VINFLUNINE;

EID: 2442585381     PISSN: 10780432     EISSN: None     Source Type: Journal    
DOI: 10.1158/1078-0432.CCR-1305-2     Document Type: Article
Times cited : (21)

References (41)
  • 1
    • 0000420523 scopus 로고    scopus 로고
    • DNA topoisomerase II inhibitors
    • Teicher BA, editor. Totowa, NJ: Humana Press Inc.
    • Pommier Y. DNA topoisomerase II inhibitors. In: Teicher BA, editor. Cancer therapeutics: experimental and clinical agents. Totowa, NJ: Humana Press Inc.; 1997. p. 153-74.
    • (1997) Cancer Therapeutics: Experimental and Clinical Agents , pp. 153-174
    • Pommier, Y.1
  • 2
    • 0033502716 scopus 로고    scopus 로고
    • Tumor cell resistance to DNA topoisomerase II inhibitors: New developments
    • Beck WT, Morgan SE, Mo YY, Bhat UG. Tumor cell resistance to DNA topoisomerase II inhibitors: new developments. Drug Resist Updat 1999;2:382-9.
    • (1999) Drug Resist Updat , vol.2 , pp. 382-389
    • Beck, W.T.1    Morgan, S.E.2    Mo, Y.Y.3    Bhat, U.G.4
  • 3
    • 0030998763 scopus 로고    scopus 로고
    • Role of oncogenes in resistance and killing by cancer therapeutic agents
    • El-Deiry WS. Role of oncogenes in resistance and killing by cancer therapeutic agents. Curr Opin Oncol 2002;9:79-87.
    • (2002) Curr Opin Oncol , vol.9 , pp. 79-87
    • El-Deiry, W.S.1
  • 4
    • 0032189251 scopus 로고    scopus 로고
    • Cellular resistance to topoisomerase-targeted drugs: From drug uptake to cell death
    • Larsen A, Skladanowski A. Cellular resistance to topoisomerase-targeted drugs: from drug uptake to cell death. Biochim Biophys Acta 1998;1400:257-74.
    • (1998) Biochim Biophys Acta , vol.1400 , pp. 257-274
    • Larsen, A.1    Skladanowski, A.2
  • 6
    • 0033962122 scopus 로고    scopus 로고
    • F11782, a novel epipodophylloid non-intercalating dual catalytic inhibitor of topoisomerases I and II with an original mechanism of action
    • Perrin D, van Hille B, Barret JM, et al. F11782, a novel epipodophylloid non-intercalating dual catalytic inhibitor of topoisomerases I and II with an original mechanism of action. Biochem Pharmacol 2000;59:807-19.
    • (2000) Biochem Pharmacol , vol.59 , pp. 807-819
    • Perrin, D.1    Van Hille, B.2    Barret, J.M.3
  • 7
    • 0142134349 scopus 로고    scopus 로고
    • A dual mechanism of action of the anticancer agent F11782 on human topoisomerase Ha
    • Jensen LH, Renodon-Cornière A, Nitiss KC, et al. A dual mechanism of action of the anticancer agent F11782 on human topoisomerase Ha. Biochem Pharmacol 2003;66:623-31.
    • (2003) Biochem Pharmacol , vol.66 , pp. 623-631
    • Jensen, L.H.1    Renodon-Cornière, A.2    Nitiss, K.C.3
  • 8
    • 0034545154 scopus 로고    scopus 로고
    • Characterization of DNA-strand breakage induced in V79 cells by F11782, a catalytic inhibitor of topoisomerases
    • Barret JM, Hill BT, Olive PL. Characterization of DNA-strand breakage induced in V79 cells by F11782, a catalytic inhibitor of topoisomerases. Br J Cancer 2000;83:1740-6.
    • (2000) Br J Cancer , vol.83 , pp. 1740-1746
    • Barret, J.M.1    Hill, B.T.2    Olive, P.L.3
  • 9
    • 0036244606 scopus 로고    scopus 로고
    • F11782, a novel catalytic inhibitor of topoisomerases I and II, induces atypical, yet cytotoxic DNA double-strand breaks in CHO-K1 cells
    • Barret JM, Etiévant C, Baudouin C, et al. F11782, a novel catalytic inhibitor of topoisomerases I and II, induces atypical, yet cytotoxic DNA double-strand breaks in CHO-K1 cells. Anticancer Res 2002;22:187-92.
    • (2002) Anticancer Res , vol.22 , pp. 187-192
    • Barret, J.M.1    Etiévant, C.2    Baudouin, C.3
  • 10
    • 0037081754 scopus 로고    scopus 로고
    • Inhibition of nucleotide excision repair and sensitisation of cells to DNA cross-linking anticancer drugs by F11782, a novel fluorinated epipodophylloid
    • Barret JM, Cadou M, Hill BT. Inhibition of nucleotide excision repair and sensitisation of cells to DNA cross-linking anticancer drugs by F11782, a novel fluorinated epipodophylloid. Biochem Pharmacol 2002;63:251-8.
    • (2002) Biochem Pharmacol , vol.63 , pp. 251-258
    • Barret, J.M.1    Cadou, M.2    Hill, B.T.3
  • 11
    • 0033676376 scopus 로고    scopus 로고
    • Preclinical antitumour activity of F11782, a novel dual catalytic inhibitor of topoisomerases
    • Kruczynski A, Etiévant C, Perrin D, et al. Preclinical antitumour activity of F11782, a novel dual catalytic inhibitor of topoisomerases. Br J Cancer 2000;83:1516-24.
    • (2000) Br J Cancer , vol.83 , pp. 1516-1524
    • Kruczynski, A.1    Etiévant, C.2    Perrin, D.3
  • 12
    • 0036638470 scopus 로고    scopus 로고
    • In vivo antitumor activity of F11782, a non-intercalating dual catalytic inhibitor of topoisomerases I and II, against a panel of human tumor xenografts
    • Kruczynski A, Ricome C, Waud W, Hill BT. In vivo antitumor activity of F11782, a non-intercalating dual catalytic inhibitor of topoisomerases I and II, against a panel of human tumor xenografts. J Exp Ther Oncol 2002;2:219-27.
    • (2002) J Exp Ther Oncol , vol.2 , pp. 219-227
    • Kruczynski, A.1    Ricome, C.2    Waud, W.3    Hill, B.T.4
  • 13
    • 0031912695 scopus 로고    scopus 로고
    • Preclinical in vivo antitumour activity of vinflunine, a novel fluorinated Vinca alkaloid
    • Kruczynski A, Colpaert F, Tarayre JP, et al. Preclinical in vivo antitumour activity of vinflunine, a novel fluorinated Vinca alkaloid. Cancer Chemother Pharmacol 1998;41:437-47.
    • (1998) Cancer Chemother Pharmacol , vol.41 , pp. 437-447
    • Kruczynski, A.1    Colpaert, F.2    Tarayre, J.P.3
  • 14
    • 0019818819 scopus 로고
    • Preclinical drug development: Rationale and methods
    • Venditti J. Preclinical drug development: rationale and methods. Semin Oncol 1981;8:349-61.
    • (1981) Semin Oncol , vol.8 , pp. 349-361
    • Venditti, J.1
  • 15
    • 0017184389 scopus 로고
    • A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding
    • Bradford M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 1976;72:248-54.
    • (1976) Anal Biochem , vol.72 , pp. 248-254
    • Bradford, M.1
  • 16
    • 0014783629 scopus 로고
    • Different inherited levels of DNA repair replication in xeroderma pigmentosum cell strains after exposure to ultraviolets irradiation
    • Bootsma D, Mudler MP, Cohen JA, Pot F. Different inherited levels of DNA repair replication in xeroderma pigmentosum cell strains after exposure to ultraviolets irradiation. Mutat Res 1970;9:507-16.
    • (1970) Mutat Res , vol.9 , pp. 507-516
    • Bootsma, D.1    Mudler, M.P.2    Cohen, J.A.3    Pot, F.4
  • 17
    • 0029999404 scopus 로고    scopus 로고
    • How to probe clinical tumor samples for P-glycoprotein and multidrug resistance-associated protein
    • Broxterman H, Kankelma J, Pinedo H. How to probe clinical tumor samples for P-glycoprotein and multidrug resistance-associated protein. Eur J Cancer 1996;32A:1024-33.
    • (1996) Eur J Cancer , vol.32 A , pp. 1024-1033
    • Broxterman, H.1    Kankelma, J.2    Pinedo, H.3
  • 19
    • 0031820395 scopus 로고    scopus 로고
    • Vinflunine (20′,20′-difluoro-3′,4′ -dihydrovinorelbine), a novel Vinca alkaloid, which participates in P-glycoprotein (Pgp)-mediated multidrug resistance in vivo and in vitro
    • Etiévant C, Barret JM, Kruczynski A, Perrin D, Hill BT. Vinflunine (20′,20′-difluoro-3′,4′-dihydrovinorelbine), a novel Vinca alkaloid, which participates in P-glycoprotein (Pgp)-mediated multidrug resistance in vivo and in vitro. Investig New Drugs 1998;16:3-17.
    • (1998) Investig New Drugs , vol.16 , pp. 3-17
    • Etiévant, C.1    Barret, J.M.2    Kruczynski, A.3    Perrin, D.4    Hill, B.T.5
  • 21
    • 0030013319 scopus 로고    scopus 로고
    • Characterization of novel human leukemic cell lines selected for resistance to merbarone, a catalytic inhibitor of DNA topoisomerase II
    • Kusumoto H, Rodgers QE, Boege F, Raimondi SC, Beck WT. Characterization of novel human leukemic cell lines selected for resistance to merbarone, a catalytic inhibitor of DNA topoisomerase II. Cancer Res 1996;56:2573-83.
    • (1996) Cancer Res , vol.56 , pp. 2573-2583
    • Kusumoto, H.1    Rodgers, Q.E.2    Boege, F.3    Raimondi, S.C.4    Beck, W.T.5
  • 23
    • 0030845812 scopus 로고    scopus 로고
    • Role of topoisomerase IIβ in the resistance of 9-OH-ellipticine-resistant Chinese hamster fibroblasts to topoisomerase II inhibitors
    • Dereuddre S, Delaporte C, Jacquemin-Sablon A. Role of topoisomerase IIβ in the resistance of 9-OH-ellipticine-resistant Chinese hamster fibroblasts to topoisomerase II inhibitors. Cancer Res 1997;57:4301-8.
    • (1997) Cancer Res , vol.57 , pp. 4301-4308
    • Dereuddre, S.1    Delaporte, C.2    Jacquemin-Sablon, A.3
  • 24
    • 0032756225 scopus 로고    scopus 로고
    • Murine transgenic cells lacking DNA topoisomerase IIβ are resistant to acridines and mitoxantrone: Analysis of cytotoxicity and cleavable complex formation
    • Errington F, Willmore E, Tilby MJ, et al. Murine transgenic cells lacking DNA topoisomerase IIβ are resistant to acridines and mitoxantrone: analysis of cytotoxicity and cleavable complex formation. Mol Pharmacol 1999;56:1309-16.
    • (1999) Mol Pharmacol , vol.56 , pp. 1309-1316
    • Errington, F.1    Willmore, E.2    Tilby, M.J.3
  • 25
    • 0005143426 scopus 로고    scopus 로고
    • Mutational analysis of topoisomerase II drug action: The yeast test tube
    • Nitiss JL. Mutational analysis of topoisomerase II drug action: the yeast test tube. Anticancer Drugs 1996;7:27-34.
    • (1996) Anticancer Drugs , vol.7 , pp. 27-34
    • Nitiss, J.L.1
  • 26
    • 0029360551 scopus 로고
    • DNA topoisomerase II mutations and resistance to anti-tumor drugs
    • Vassetzky YS, Alghisi GC, Gasser SM. DNA topoisomerase II mutations and resistance to anti-tumor drugs. BioEssays 1995;17:767-74.
    • (1995) BioEssays , vol.17 , pp. 767-774
    • Vassetzky, Y.S.1    Alghisi, G.C.2    Gasser, S.M.3
  • 27
    • 0033635293 scopus 로고    scopus 로고
    • Characterization of the biological and biochemical activities of F11782 and bisdioxopiperazines, ICRF-187 and ICRF-193, two types of topoisomerase II catalytic inhibitors with distinctive mechanisms of action
    • van Hille B, Etiévant C, Barret JM, Kruczynski A, Hill BT. Characterization of the biological and biochemical activities of F11782 and bisdioxopiperazines, ICRF-187 and ICRF-193, two types of topoisomerase II catalytic inhibitors with distinctive mechanisms of action. Anticancer Drugs 2000;11:829-41.
    • (2000) Anticancer Drugs , vol.11 , pp. 829-841
    • Van Hille, B.1    Etiévant, C.2    Barret, J.M.3    Kruczynski, A.4    Hill, B.T.5
  • 28
    • 0030713362 scopus 로고    scopus 로고
    • Anthracyclines in the treatment of cancer: An overview
    • Hotobagyi GN. Anthracyclines in the treatment of cancer: an overview. Drugs 1997;54:1-7.
    • (1997) Drugs , vol.54 , pp. 1-7
    • Hotobagyi, G.N.1
  • 29
    • 0030476665 scopus 로고    scopus 로고
    • Acquired resistance of human breast cancer MCF-7/C4 cells with normal topoisomerase I and elevated DNA repair
    • Fujimori A, Gupta M, Hoki Y, Pommier Y. Acquired resistance of human breast cancer MCF-7/C4 cells with normal topoisomerase I and elevated DNA repair. Mol Pharmacol 1996;50:1472-8.
    • (1996) Mol Pharmacol , vol.50 , pp. 1472-1478
    • Fujimori, A.1    Gupta, M.2    Hoki, Y.3    Pommier, Y.4
  • 30
    • 0036098112 scopus 로고    scopus 로고
    • Synergistic effects of F11782, a novel dual catalytic inhibitor of topoisomerases I and II, in combination with other anticancer agents
    • Barret JM, Kruczynski A, Etiévant C, Hill BT. Synergistic effects of F11782, a novel dual catalytic inhibitor of topoisomerases I and II, in combination with other anticancer agents. Cancer Chemother Pharmacol 2002;49:479-86.
    • (2002) Cancer Chemother Pharmacol , vol.49 , pp. 479-486
    • Barret, J.M.1    Kruczynski, A.2    Etiévant, C.3    Hill, B.T.4
  • 31
    • 0028141961 scopus 로고
    • Messenger RNA levels of XPAC and ERCC1 in ovarian cancer tissue correlate with response to platinum-based chemotherapy
    • Dabholkar M, Vionnet J, Bostickbruton F, Yu J, Reed E. Messenger RNA levels of XPAC and ERCC1 in ovarian cancer tissue correlate with response to platinum-based chemotherapy. J Clin Investig 1994;94:703-8.
    • (1994) J Clin Investig , vol.94 , pp. 703-708
    • Dabholkar, M.1    Vionnet, J.2    Bostickbruton, F.3    Yu, J.4    Reed, E.5
  • 32
    • 0029773392 scopus 로고    scopus 로고
    • Nucleotide excision repair genes as determinants of cellular sensitivity to cyclophosphamide analogs
    • Anderson B, Sadeghi T, Siciliano M, Legerski R, Murray D. Nucleotide excision repair genes as determinants of cellular sensitivity to cyclophosphamide analogs. Cancer Chemother Pharmacol 1996;38:406-16.
    • (1996) Cancer Chemother Pharmacol , vol.38 , pp. 406-416
    • Anderson, B.1    Sadeghi, T.2    Siciliano, M.3    Legerski, R.4    Murray, D.5
  • 33
    • 0029890253 scopus 로고    scopus 로고
    • Sensitivity of CHO mutant cell lines with specific defects in nucleotides excision repair to different anti-cancer agents
    • Damia G, Imperatori L, Stefanini M, D'Incalci M. Sensitivity of CHO mutant cell lines with specific defects in nucleotides excision repair to different anti-cancer agents. Int J Cancer 1996;66:779-83.
    • (1996) Int J Cancer , vol.66 , pp. 779-783
    • Damia, G.1    Imperatori, L.2    Stefanini, M.3    D'Incalci, M.4
  • 34
    • 0027372625 scopus 로고
    • Cisplatin sensitivity/resistance in UV repair-deficient Chinese hamster ovary cells of complementation groups 1 and 3
    • Lee K, Parker R, Bohr V, Cornelison T, Reed E. Cisplatin sensitivity/resistance in UV repair-deficient Chinese hamster ovary cells of complementation groups 1 and 3. Carcinogenesis (Lond) 1993;14:2177-80.
    • (1993) Carcinogenesis (Lond) , vol.14 , pp. 2177-2180
    • Lee, K.1    Parker, R.2    Bohr, V.3    Cornelison, T.4    Reed, E.5
  • 35
    • 17944374027 scopus 로고    scopus 로고
    • Antiproliferative activity of ecteinascidin 743 is dependent upon transcription-coupled nucleotide-excision repair
    • Takebayashi Y, Pourquier P, Zimonjic D, et al. Antiproliferative activity of ecteinascidin 743 is dependent upon transcription-coupled nucleotide-excision repair. Nat Med 2001;7:961-6.
    • (2001) Nat Med , vol.7 , pp. 961-966
    • Takebayashi, Y.1    Pourquier, P.2    Zimonjic, D.3
  • 36
    • 0036021010 scopus 로고    scopus 로고
    • Ecteinascidin 743: A novel anticancer drug with a unique mechanism of action
    • Aune G, Furuta T, Pommier Y. Ecteinascidin 743: a novel anticancer drug with a unique mechanism of action. Anti-Cancer Drugs 2002;13:545-55.
    • (2002) Anti-Cancer Drugs , vol.13 , pp. 545-555
    • Aune, G.1    Furuta, T.2    Pommier, Y.3
  • 37
    • 2442631315 scopus 로고    scopus 로고
    • Unexpected complexities of pathway interactions in repair of oxidative damage
    • Cooper P. Unexpected complexities of pathway interactions in repair of oxidative damage. Proc Am Assoc Cancer Res 2002;43:1180.
    • (2002) Proc Am Assoc Cancer Res , vol.43 , pp. 1180
    • Cooper, P.1
  • 38
    • 0031025997 scopus 로고    scopus 로고
    • Defective transcription-coupled repair of oxidative base damage in Cockayne syndrome patients from XP group G
    • Cooper P, Nouspikel T, Clarkson S, Li G, Leadon S. Defective transcription-coupled repair of oxidative base damage in Cockayne syndrome patients from XP group G. Science (Wash DC) 1997;275:990-3.
    • (1997) Science (Wash DC) , vol.275 , pp. 990-993
    • Cooper, P.1    Nouspikel, T.2    Clarkson, S.3    Li, G.4    Leadon, S.5
  • 39
    • 0027102396 scopus 로고
    • In vitro evolution of cisplatin/DNA monoadducts into diadducts is dependent upon super-helical density
    • Bouayadi K, Calson P, Pedrini AM, Salles B. In vitro evolution of cisplatin/DNA monoadducts into diadducts is dependent upon super-helical density. Biochem Biophys Res Commun 1992;189:111-8.
    • (1992) Biochem Biophys Res Commun , vol.189 , pp. 111-118
    • Bouayadi, K.1    Calson, P.2    Pedrini, A.M.3    Salles, B.4
  • 40
    • 0034660061 scopus 로고    scopus 로고
    • Crystal structure of NaeI: An evolutionary bridge between DNA endonuclease and topoisomerase
    • Huai Q, Colandene JD, Chen Y, et al. Crystal structure of NaeI: an evolutionary bridge between DNA endonuclease and topoisomerase. EMBO J 2000;19:3110-8.
    • (2000) EMBO J , vol.19 , pp. 3110-3118
    • Huai, Q.1    Colandene, J.D.2    Chen, Y.3
  • 41
    • 0033605159 scopus 로고    scopus 로고
    • Conserved residues of human XPG protein important for nuclease activity and function in nucleotide excision repair
    • Constantinou A, Gunz D, Evans E, et al. Conserved residues of human XPG protein important for nuclease activity and function in nucleotide excision repair. J Biol Chem 1999;274:5637-48.
    • (1999) J Biol Chem , vol.274 , pp. 5637-5648
    • Constantinou, A.1    Gunz, D.2    Evans, E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.