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Volumn 53, Issue 12, 1997, Pages 1843-1853

Characterization of a chinese hamster ovary cell line with acquired resistance to the bisdioxopiperazine dexrazoxane (ICRF-187) catalytic inhibitor, of topoisomerase II

Author keywords

Bisdioxopiperazine; Dexrazoxane; ICRF 193; ICRF 187; Resistant cell; Topoisomerase II

Indexed keywords

1,2 BIS(3,5 DIOXOPIPERAZIN 1 YL)ETHANE; ANTHRACYCLINE ANTIBIOTIC AGENT; DAUNORUBICIN; DNA TOPOISOMERASE (ATP HYDROLYSING); DOXORUBICIN; EPIRUBICIN; ETOPOSIDE; IDARUBICIN; RAZOXANE;

EID: 0030739460     PISSN: 00062952     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0006-2952(97)00013-0     Document Type: Article
Times cited : (45)

References (47)
  • 1
    • 0026425654 scopus 로고
    • Inhibition of intracellular topoisomerase II by antitumor bis(2,6-dioxopiperazine) derivatives: Mode of cell growth inhibition distinct from that of cleavable complex-forming type inhibitors
    • Ishida R, Miki T, Narica T, Yui R, Sato M, Utsumi KR, Tanabe K and Andoh T, Inhibition of intracellular topoisomerase II by antitumor bis(2,6-dioxopiperazine) derivatives: Mode of cell growth inhibition distinct from that of cleavable complex-forming type inhibitors. Cancer Res 51: 4909-4916, 1991.
    • (1991) Cancer Res , vol.51 , pp. 4909-4916
    • Ishida, R.1    Miki, T.2    Narica, T.3    Yui, R.4    Sato, M.5    Utsumi, K.R.6    Tanabe, K.7    Andoh, T.8
  • 2
    • 0028810791 scopus 로고
    • A QSAR study comparing the cytotoxicity and DNA topoisomerase II inhibitory effects of bisdioxopiperazine analogs of ICRF-187 (dexrazoxane)
    • Hasinoff BB, Kuschak TI, Yalowich JC and Creighton AM, A QSAR study comparing the cytotoxicity and DNA topoisomerase II inhibitory effects of bisdioxopiperazine analogs of ICRF-187 (dexrazoxane). Biochem Pharmacol 50: 953-958, 1995.
    • (1995) Biochem Pharmacol , vol.50 , pp. 953-958
    • Hasinoff, B.B.1    Kuschak, T.I.2    Yalowich, J.C.3    Creighton, A.M.4
  • 4
    • 0028345406 scopus 로고
    • Antitumor bisdioxopiperazines inhibit yeast DNA topoisomerase II by trapping the enzyme in the form of a closed protein clamp
    • Roca J, Ishida R, Berger JM, Andoh T and Wang JC, Antitumor bisdioxopiperazines inhibit yeast DNA topoisomerase II by trapping the enzyme in the form of a closed protein clamp. Proc Natl Acad Sci USA 91: 1781-1785, 1994.
    • (1994) Proc Natl Acad Sci USA , vol.91 , pp. 1781-1785
    • Roca, J.1    Ishida, R.2    Berger, J.M.3    Andoh, T.4    Wang, J.C.5
  • 5
    • 0027214092 scopus 로고
    • Antagonistic effect of the cardioprotector (+)-1,2-bis(3,5-dioxopiperazinyl-1-yl)propane (ICRF-187) on DNA breaks and cytotoxicity induced by the topoisomerase II directed drugs daunorubicin and etoposide (VP-16)
    • Sehested M, Jensen PB, Sorensen BS, Holm B, Friche E and Demant EJF, Antagonistic effect of the cardioprotector (+)-1,2-bis(3,5-dioxopiperazinyl-1-yl)propane (ICRF-187) on DNA breaks and cytotoxicity induced by the topoisomerase II directed drugs daunorubicin and etoposide (VP-16). Biochem Pharmacol 46: 389-393, 1993.
    • (1993) Biochem Pharmacol , vol.46 , pp. 389-393
    • Sehested, M.1    Jensen, P.B.2    Sorensen, B.S.3    Holm, B.4    Friche, E.5    Demant, E.J.F.6
  • 6
    • 0014691658 scopus 로고
    • Antitumour activity in a series of bisdiketopiperazines
    • Creighton AM, Hellmann K and Whitecross S, Antitumour activity in a series of bisdiketopiperazines. Nature 22: 384-385, 1969.
    • (1969) Nature , vol.22 , pp. 384-385
    • Creighton, A.M.1    Hellmann, K.2    Whitecross, S.3
  • 8
    • 0028093440 scopus 로고
    • Pharmacodynamics of the hydrolysis-activation of the cardioprotective agent (+)-1,2-bis(3,5-dioxopiperazinyl-1-yl)propane
    • Hasinoff BB, Pharmacodynamics of the hydrolysis-activation of the cardioprotective agent (+)-1,2-bis(3,5-dioxopiperazinyl-1-yl)propane. J Pharm Sci 83: 64-67, 1994.
    • (1994) J Pharm Sci , vol.83 , pp. 64-67
    • Hasinoff, B.B.1
  • 9
    • 0027740137 scopus 로고
    • The one-ring open hydrolysis product intermediates of the cardioprotective agent ICRF-187 (dexrazoxane) displace iron from iron-anthracycline complexes
    • Buss JL and Hasinoff BB, The one-ring open hydrolysis product intermediates of the cardioprotective agent ICRF-187 (dexrazoxane) displace iron from iron-anthracycline complexes. Agents Actions 40: 86-95, 1993.
    • (1993) Agents Actions , vol.40 , pp. 86-95
    • Buss, J.L.1    Hasinoff, B.B.2
  • 10
    • 0027381810 scopus 로고
    • When good enzymes go bad: Conversion of topoisomerase II to a cellular toxin by anti-neoplastic drugs
    • Corbett AH and Osheroff N, When good enzymes go bad: Conversion of topoisomerase II to a cellular toxin by anti-neoplastic drugs. Chem Res Toxicol 6: 585-597, 1993.
    • (1993) Chem Res Toxicol , vol.6 , pp. 585-597
    • Corbett, A.H.1    Osheroff, N.2
  • 14
    • 0029982836 scopus 로고    scopus 로고
    • Collateral sensitivity to the bisdioxopiperazine dexrazoxane (ICRF-187) in etoposide (VP-16) resistant human leukemia K562 cells
    • Fattman C, Allan WP, Hasinoff BB and Yalowich JC, Collateral sensitivity to the bisdioxopiperazine dexrazoxane (ICRF-187) in etoposide (VP-16) resistant human leukemia K562 cells. Biochem Pharmacol 52: 635-642, 1996.
    • (1996) Biochem Pharmacol , vol.52 , pp. 635-642
    • Fattman, C.1    Allan, W.P.2    Hasinoff, B.B.3    Yalowich, J.C.4
  • 15
    • 0029796045 scopus 로고    scopus 로고
    • The effect of dexrazoxane (ICRF-187) on doxorubicin and daunorubicin-mediated growth inhibition of Chinese hamster ovary (CHO) cells
    • Hasinoff BB, Yalowich JC, Ling Y and Buss JL, The effect of dexrazoxane (ICRF-187) on doxorubicin and daunorubicin-mediated growth inhibition of Chinese hamster ovary (CHO) cells. Anticancer Drugs 7: 558-567, 1996.
    • (1996) Anticancer Drugs , vol.7 , pp. 558-567
    • Hasinoff, B.B.1    Yalowich, J.C.2    Ling, Y.3    Buss, J.L.4
  • 16
    • 0030007125 scopus 로고    scopus 로고
    • Mapping of DNA topoisomerase II poisons (etoposide, clerocidin) and catalytic inhibitors (aclarubicin, ICRF-187) to four distinct steps in the topoisomerase II catalytic cycle
    • Sehested M and Jensen PB, Mapping of DNA topoisomerase II poisons (etoposide, clerocidin) and catalytic inhibitors (aclarubicin, ICRF-187) to four distinct steps in the topoisomerase II catalytic cycle. Biochem Pharmacol 51: 879-886, 1996.
    • (1996) Biochem Pharmacol , vol.51 , pp. 879-886
    • Sehested, M.1    Jensen, P.B.2
  • 19
    • 0028141994 scopus 로고
    • Reduced phosphorylation of topoisomerase II in etoposide-resistant human leukemia K562 cells
    • Ritke MK, Allan WP, Fattman C, Gunduz NN and Yalowich JC, Reduced phosphorylation of topoisomerase II in etoposide-resistant human leukemia K562 cells. Mol Pharmacol 46: 58-66, 1994.
    • (1994) Mol Pharmacol , vol.46 , pp. 58-66
    • Ritke, M.K.1    Allan, W.P.2    Fattman, C.3    Gunduz, N.N.4    Yalowich, J.C.5
  • 20
    • 0028325365 scopus 로고
    • Altered stability of etoposide-induced topoisomerase II-DNA complexes in resistant human leukemia K562 cells
    • Ritke MK, Roberts D, Allan WP, Raymond J, Bergoltz VV and Yalowich JC, Altered stability of etoposide-induced topoisomerase II-DNA complexes in resistant human leukemia K562 cells. Br J Cancer 69: 687-697, 1994.
    • (1994) Br J Cancer , vol.69 , pp. 687-697
    • Ritke, M.K.1    Roberts, D.2    Allan, W.P.3    Raymond, J.4    Bergoltz, V.V.5    Yalowich, J.C.6
  • 21
    • 0022524870 scopus 로고
    • A quantitative decatenation assay for type II topoisomerases
    • Sahai BM and Kaplan JG, A quantitative decatenation assay for type II topoisomerases. Anal Biochem 156: 364-379, 1986.
    • (1986) Anal Biochem , vol.156 , pp. 364-379
    • Sahai, B.M.1    Kaplan, J.G.2
  • 22
    • 0020398870 scopus 로고
    • Metal binding by pharmaceuticals. Part 2. Interactions of Ca(II), Cu(II), Fe(II), Mg(II), Mn(II) and Zn(II) with the intracellular hydrolysis products of the antitumor agent ICRF-159 and its inactive homologue ICRF-192
    • Huang Z-X, May PM, Quinlan KM, Williams DR and Creighton AM, Metal binding by pharmaceuticals. Part 2. Interactions of Ca(II), Cu(II), Fe(II), Mg(II), Mn(II) and Zn(II) with the intracellular hydrolysis products of the antitumor agent ICRF-159 and its inactive homologue ICRF-192. Agents Actions 12: 536-542, 1982.
    • (1982) Agents Actions , vol.12 , pp. 536-542
    • Huang, Z.-X.1    May, P.M.2    Quinlan, K.M.3    Williams, D.R.4    Creighton, A.M.5
  • 23
    • 0026425619 scopus 로고
    • Inhibition of topoisomerase II by antitumor agents bis(2,6-dioxopiperazine) derivatives
    • Tanabe K, Ikegami Y, Ishida R and Andoh T, Inhibition of topoisomerase II by antitumor agents bis(2,6-dioxopiperazine) derivatives. Cancer Res 51: 4903-4908, 1991.
    • (1991) Cancer Res , vol.51 , pp. 4903-4908
    • Tanabe, K.1    Ikegami, Y.2    Ishida, R.3    Andoh, T.4
  • 25
    • 0027194055 scopus 로고
    • Different modes of anthracycline interaction with topoisomerase II. Separate structures critical for DNA-cleavage, and for overcoming topoisomerase II-related drug resistance
    • Jensen PB, Sorensen BS, Sehested M, Demant EJF, Kjeldsen E, Friche E and Hansen HH, Different modes of anthracycline interaction with topoisomerase II. Separate structures critical for DNA-cleavage, and for overcoming topoisomerase II-related drug resistance. Biochem Pharmacol 45: 2025-2035, 1993.
    • (1993) Biochem Pharmacol , vol.45 , pp. 2025-2035
    • Jensen, P.B.1    Sorensen, B.S.2    Sehested, M.3    Demant, E.J.F.4    Kjeldsen, E.5    Friche, E.6    Hansen, H.H.7
  • 27
    • 0027965136 scopus 로고
    • Defining functional drug-interaction domains on topoisomerase II by exploiting mechanistic differences between drug classes
    • Osheroff N, Corbett AH, Elsea SH and Westergaard M, Defining functional drug-interaction domains on topoisomerase II by exploiting mechanistic differences between drug classes. Cancer Chemother Pharmacol 34 (Suppl): S19-S25, 1994.
    • (1994) Cancer Chemother Pharmacol , vol.34 , Issue.SUPPL.
    • Osheroff, N.1    Corbett, A.H.2    Elsea, S.H.3    Westergaard, M.4
  • 28
    • 0029144134 scopus 로고
    • Topoisomerase poisons: Harnessing the dark side of enzyme mechanism
    • Froelich-Ammon SJ and Osheroff N, Topoisomerase poisons: Harnessing the dark side of enzyme mechanism. J Biol Chem 270: 21429-21432, 1995.
    • (1995) J Biol Chem , vol.270 , pp. 21429-21432
    • Froelich-Ammon, S.J.1    Osheroff, N.2
  • 30
    • 0028063201 scopus 로고
    • Antitumor drug fostriecin inhibits the mitotic entry checkpoint and protein phosphatases 1 and 2A
    • Roberge M, Tudan V, Hung SMF, Harder KW, Jirik FR and Anderson H, Antitumor drug fostriecin inhibits the mitotic entry checkpoint and protein phosphatases 1 and 2A. Cancer Res 54: 6115-6121, 1994.
    • (1994) Cancer Res , vol.54 , pp. 6115-6121
    • Roberge, M.1    Tudan, V.2    Hung, S.M.F.3    Harder, K.W.4    Jirik, F.R.5    Anderson, H.6
  • 32
    • 0029046736 scopus 로고
    • DNA topoisomerase II is the molecular target of bisdioxopiperazine derivatives ICRF-159 and ICRF-193 in Saccharomyces cerevisiae
    • Ishida R, Hamatake M, Wasserman RA, Nitiss JL, Wang JC and Andoh T, DNA topoisomerase II is the molecular target of bisdioxopiperazine derivatives ICRF-159 and ICRF-193 in Saccharomyces cerevisiae. Cancer Res 55: 2299-2303, 1995.
    • (1995) Cancer Res , vol.55 , pp. 2299-2303
    • Ishida, R.1    Hamatake, M.2    Wasserman, R.A.3    Nitiss, J.L.4    Wang, J.C.5    Andoh, T.6
  • 33
    • 0026448670 scopus 로고
    • The capture of a DNA double helix by an ATP-dependent protein clamp: A key step in DNA transport by type II DNA topoisomerases
    • Roca J and Wang JC, The capture of a DNA double helix by an ATP-dependent protein clamp: A key step in DNA transport by type II DNA topoisomerases. Cell 71: 833-840, 1992.
    • (1992) Cell , vol.71 , pp. 833-840
    • Roca, J.1    Wang, J.C.2
  • 34
    • 0028070915 scopus 로고
    • Mechanistic studies of amsacrine-resistant derivatives of DNA topisomerase II
    • Wasserman RA and Wang JC, Mechanistic studies of amsacrine-resistant derivatives of DNA topisomerase II. J Biol Chem 269: 20943-20951, 1994.
    • (1994) J Biol Chem , vol.269 , pp. 20943-20951
    • Wasserman, R.A.1    Wang, J.C.2
  • 37
    • 0028819988 scopus 로고
    • Selective use of an alternative stop codon and polyadenylation signal within intron sequences leads to a truncated topoisomerase IIα
    • Harker WG, Slade DL, Parr RL and Holguin MH, Selective use of an alternative stop codon and polyadenylation signal within intron sequences leads to a truncated topoisomerase IIα. Cancer Res 55: 4962-4971, 1995.
    • (1995) Cancer Res , vol.55 , pp. 4962-4971
    • Harker, W.G.1    Slade, D.L.2    Parr, R.L.3    Holguin, M.H.4
  • 38
    • 0028091270 scopus 로고
    • Altered subcellular distribution of topoisomerase IIα in a drug-resistant human small cell lung cancer cell line
    • Feldhoff PW, Mirski SEL, Cole SPC and Sullivan DM, Altered subcellular distribution of topoisomerase IIα in a drug-resistant human small cell lung cancer cell line. Cancer Res 54: 756-762, 1994.
    • (1994) Cancer Res , vol.54 , pp. 756-762
    • Feldhoff, P.W.1    Mirski, S.E.L.2    Cole, S.P.C.3    Sullivan, D.M.4
  • 39
    • 0029821995 scopus 로고    scopus 로고
    • Multidrug resistance mediated by the multidrug resistance protein (MRP) gene
    • Lautier D, Canitrot Y, Deeley RG and Cole SPC, Multidrug resistance mediated by the multidrug resistance protein (MRP) gene. Biochem Pharmacol 52: 967-977, 1996.
    • (1996) Biochem Pharmacol , vol.52 , pp. 967-977
    • Lautier, D.1    Canitrot, Y.2    Deeley, R.G.3    Cole, S.P.C.4
  • 40
    • 0029007898 scopus 로고
    • DNA topoisomerase II expression, stability, and phosphorylation in two VM-26-resistant human leukemic CEM sublines
    • Chen M and Beck WT, DNA topoisomerase II expression, stability, and phosphorylation in two VM-26-resistant human leukemic CEM sublines. Oncol Res 7: 103-111, 1995.
    • (1995) Oncol Res , vol.7 , pp. 103-111
    • Chen, M.1    Beck, W.T.2
  • 41
    • 0029830692 scopus 로고    scopus 로고
    • Resistance to etoposide in human leukemia HL-60 cells: Reduction in drug-induced DNA cleavage associated with hypophosphorylation of topoisomerase II phosphopeptides
    • Ganapathi R, Constantinou A, Kamath N, Dubyak G, Grabowski D and Krivacic K, Resistance to etoposide in human leukemia HL-60 cells: Reduction in drug-induced DNA cleavage associated with hypophosphorylation of topoisomerase II phosphopeptides. Mol Pharmacol 50: 243-248, 1996.
    • (1996) Mol Pharmacol , vol.50 , pp. 243-248
    • Ganapathi, R.1    Constantinou, A.2    Kamath, N.3    Dubyak, G.4    Grabowski, D.5    Krivacic, K.6
  • 42
    • 0026378295 scopus 로고
    • Increased phosphorylation of DNA topoisomerase II in etoposide-resistant mutants of human cancer KB cells
    • Takano H, Kohno K, Ono M, Uchida Y and Kuwano M, Increased phosphorylation of DNA topoisomerase II in etoposide-resistant mutants of human cancer KB cells. Cancer Res 51: 3951-3957, 1991.
    • (1991) Cancer Res , vol.51 , pp. 3951-3957
    • Takano, H.1    Kohno, K.2    Ono, M.3    Uchida, Y.4    Kuwano, M.5
  • 43
    • 0029037591 scopus 로고
    • Altered topoisomerase I and II activities in suramin-resistant lung fibrosarcoma cells
    • Lelievre S, Benchokroun Y and Larsen AK, Altered topoisomerase I and II activities in suramin-resistant lung fibrosarcoma cells. Mol Pharmacol 47: 898-906, 1995.
    • (1995) Mol Pharmacol , vol.47 , pp. 898-906
    • Lelievre, S.1    Benchokroun, Y.2    Larsen, A.K.3
  • 44
    • 0020459342 scopus 로고
    • Isolation and characterization of a subline of CHO cells with induced resistance to ICRF 159
    • Kenwrick SJ and Creighton AM, Isolation and characterization of a subline of CHO cells with induced resistance to ICRF 159. Br J Cancer 46: 504-505, 1982.
    • (1982) Br J Cancer , vol.46 , pp. 504-505
    • Kenwrick, S.J.1    Creighton, A.M.2
  • 45
    • 0343268772 scopus 로고    scopus 로고
    • CHO cells resistant to the topoisomerase II catalytic inhibitor ICRF-159 have altered drug-DNA-enzyme binding capability
    • Sehested M, Holm B, Kenwrick S and Creighton AM, CHO cells resistant to the topoisomerase II catalytic inhibitor ICRF-159 have altered drug-DNA-enzyme binding capability. Proc Am Assoc Cancer Res 37: 436, 1996.
    • (1996) Proc Am Assoc Cancer Res , vol.37 , pp. 436
    • Sehested, M.1    Holm, B.2    Kenwrick, S.3    Creighton, A.M.4
  • 46
    • 0343704443 scopus 로고
    • Mechanistic studies with a cell line resistant to ICRF-159
    • White K and Creighton AM, Mechanistic studies with a cell line resistant to ICRF-159. Br J Cancer 34: 323, 1976.
    • (1976) Br J Cancer , vol.34 , pp. 323
    • White, K.1    Creighton, A.M.2


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