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Volumn 11, Issue 4, 2005, Pages 1608-1617

Formation and antitumor activity of PNU-159682, a major metabolite of nemorubicin in human liver microsomes

Author keywords

[No Author keywords available]

Indexed keywords

3' DEAMINO 3'',4' ANHYDRO (2'' METHOXY 3'' OXY 4'' MORPHOLINYL)DOXORUBICIN; ANTINEOPLASTIC AGENT; COMPLEMENTARY DNA; CYTOCHROME P450; CYTOCHROME P450 3A; CYTOCHROME P450 3A4; DOXORUBICIN; DRUG METABOLITE; KETOCONAZOLE; MONOCLONAL ANTIBODY; NEMORUBICIN; PNU 159682; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE; TROLEANDOMYCIN; UNCLASSIFIED DRUG;

EID: 14644396570     PISSN: 10780432     EISSN: None     Source Type: Journal    
DOI: 10.1158/1078-0432.CCR-04-1845     Document Type: Article
Times cited : (57)

References (47)
  • 1
    • 0026553237 scopus 로고
    • In vivo anti-tumour activity of FCE 23762, a methoxymorpholinyl derivative of doxorubicin active on doxorubicin-resistant tumour cells
    • Ripamonti M, Pezzoni G, Pesenti E, et al. In vivo anti-tumour activity of FCE 23762, a methoxymorpholinyl derivative of doxorubicin active on doxorubicin-resistant tumour cells. Br J Cancer 1992;65:703-7.
    • (1992) Br J Cancer , vol.65 , pp. 703-707
    • Ripamonti, M.1    Pezzoni, G.2    Pesenti, E.3
  • 2
    • 0030716194 scopus 로고    scopus 로고
    • Mechanisms for high methoxymorpholino doxorubicin cytotoxicity in doxorubicin-resistant tumor cell lines
    • Bakker M, Renes J, Groenhuijzen A, et al. Mechanisms for high methoxymorpholino doxorubicin cytotoxicity in doxorubicin-resistant tumor cell lines. Int J Cancer 1997;73:362-6.
    • (1997) Int J Cancer , vol.73 , pp. 362-366
    • Bakker, M.1    Renes, J.2    Groenhuijzen, A.3
  • 3
    • 0028100220 scopus 로고
    • Growth-inhibitory properties of novel anthracyclines in human leukemic cell lines expressing either Pgp-MDR or at-MDR
    • Mariani M, Capolongo L, Suarato A, et al. Growth-inhibitory properties of novel anthracyclines in human leukemic cell lines expressing either Pgp-MDR or at-MDR. Invest New Drugs 1994;12:93-7.
    • (1994) Invest New Drugs , vol.12 , pp. 93-97
    • Mariani, M.1    Capolongo, L.2    Suarato, A.3
  • 4
    • 0027204231 scopus 로고
    • 3′-Deamino-3′-(2-methoxy-4-morpholinyl)-doxorubicin (FCE 23762): A new anthracycline derivative with enhanced cytotoxicity and reduced cardiotoxicity
    • Danesi R, Agen C, Grandi M, Nardini V, Bevilacqua G, Del Tacca M. 3′-Deamino-3′-(2-methoxy-4-morpholinyl)-doxorubicin (FCE 23762): a new anthracycline derivative with enhanced cytotoxicity and reduced cardiotoxicity. Eur J Cancer 1993;11:1560-5.
    • (1993) Eur J Cancer , vol.11 , pp. 1560-1565
    • Danesi, R.1    Agen, C.2    Grandi, M.3    Nardini, V.4    Bevilacqua, G.5    Del Tacca, M.6
  • 5
    • 14644439128 scopus 로고    scopus 로고
    • Efficacy of nemorubicin (MMDX) administered with iodinated oil via hepatic artery (IHA) to patients with unresectable primary hepatocellular carcinoma (HCC): Phase II trial
    • 28 September-1 October; Geneva, Switzerland
    • Sun Y, et al. Efficacy of nemorubicin (MMDX) administered with iodinated oil via hepatic artery (IHA) to patients with unresectable primary hepatocellular carcinoma (HCC): phase II trial. Abstract presented to the 16th EORTC-NCI-AACR Symposium on Molecular Targets and Cancer Therapeutics; 28 September-1 October 2004; Geneva, Switzerland.
    • (2004) 16th EORTC-NCI-AACR Symposium on Molecular Targets and Cancer Therapeutics
    • Sun, Y.1
  • 6
    • 0029023640 scopus 로고
    • Phase I clinical and pharmacokinetic study of 3′-deamino-3′- (2-methoxy-4-morpholinyl)doxorubicin (FCE 23762)
    • Vasey PA, Bissett D, Strolin-Benedetti M, et al. Phase I clinical and pharmacokinetic study of 3′-deamino-3′-(2-methoxy-4-morpholinyl) doxorubicin (FCE 23762). Cancer Res 1995;55:2090-6.
    • (1995) Cancer Res , vol.55 , pp. 2090-2096
    • Vasey, P.A.1    Bissett, D.2    Strolin-Benedetti, M.3
  • 7
    • 0032982751 scopus 로고    scopus 로고
    • Delivery of methoxymorpholinyl doxorubicin by interleukin 2-activated NK cells: Effect in mice bearing hepatic metastases
    • Quintieri L, Rosato A, Amboldi N, et al. Delivery of methoxymorpholinyl doxorubicin by interleukin 2-activated NK cells: effect in mice bearing hepatic metastases. Br J Cancer 1999;79:1067-73.
    • (1999) Br J Cancer , vol.79 , pp. 1067-1073
    • Quintieri, L.1    Rosato, A.2    Amboldi, N.3
  • 8
    • 0028200049 scopus 로고
    • Metabolic conversion of methoxymorpholinyl doxorubicin: From a DNA strand breaker to a DNA cross-linker
    • Lau DH, Duran GE, Lewis AD, Sikic BI. Metabolic conversion of methoxymorpholinyl doxorubicin: from a DNA strand breaker to a DNA cross-linker. Br J Cancer 1994;70:79-84.
    • (1994) Br J Cancer , vol.70 , pp. 79-84
    • Lau, D.H.1    Duran, G.E.2    Lewis, A.D.3    Sikic, B.I.4
  • 9
    • 0034083806 scopus 로고    scopus 로고
    • In vivo antitumor activity and host toxicity of methoxymorpholinyl doxorubicin: Role of cytochrome P450 3A
    • Quintieri L, Rosato A, Napoli E, et al. In vivo antitumor activity and host toxicity of methoxymorpholinyl doxorubicin: role of cytochrome P450 3A. Cancer Res 2000;60:3232-8.
    • (2000) Cancer Res , vol.60 , pp. 3232-3238
    • Quintieri, L.1    Rosato, A.2    Napoli, E.3
  • 10
    • 0037226113 scopus 로고    scopus 로고
    • Identification of novel enzyme-prodrug combinations for use in cytochrome P450-based gene therapy for cancer
    • Baldwin A, Huang Z, Jounaidi Y, Waxman DJ. Identification of novel enzyme-prodrug combinations for use in cytochrome P450-based gene therapy for cancer. Arch Biochem Biophys 2003;409:197-206.
    • (2003) Arch Biochem Biophys , vol.409 , pp. 197-206
    • Baldwin, A.1    Huang, Z.2    Jounaidi, Y.3    Waxman, D.J.4
  • 11
    • 0033844217 scopus 로고    scopus 로고
    • Species-differences in disposition and reductive metabolism of methoxymorpholinodoxorubicin (PNU 152243), a new potential anticancer agent
    • Breda M, Strolin-Benedetti M, Battaglia R, et al. Species-differences in disposition and reductive metabolism of methoxymorpholinodoxorubicin (PNU 152243), a new potential anticancer agent. Pharmacol Res 2000;41:239-48.
    • (2000) Pharmacol Res , vol.41 , pp. 239-248
    • Breda, M.1    Strolin-Benedetti, M.2    Battaglia, R.3
  • 12
    • 0024355564 scopus 로고
    • Comparative activity of anthracycline 13-dihydrometabolites against rat glioblastoma cells in culture
    • Schott B, Robert J. Comparative activity of anthracycline 13-dihydrometabolites against rat glioblastoma cells in culture. Biochem Pharmacol 1989;38:4069-74.
    • (1989) Biochem Pharmacol , vol.38 , pp. 4069-4074
    • Schott, B.1    Robert, J.2
  • 13
    • 0032834824 scopus 로고    scopus 로고
    • Phase I clinical and pharmacological study of oral methoxymorpholinyl doxorubicin (PNU 152243)
    • Sessa C, Zucchetti M, Ghielmini M, et al. Phase I clinical and pharmacological study of oral methoxymorpholinyl doxorubicin (PNU 152243). Cancer Chemother Pharmacol 1999;44:403-10.
    • (1999) Cancer Chemother Pharmacol , vol.44 , pp. 403-410
    • Sessa, C.1    Zucchetti, M.2    Ghielmini, M.3
  • 15
    • 0029620446 scopus 로고
    • Inhibitory and non-inhibitory monoclonal antibodies to human cytochrome P450 3A3/4
    • Gelboin HV, Krausz KW, Goldfarb I, et al. Inhibitory and non-inhibitory monoclonal antibodies to human cytochrome P450 3A3/4. Biochem Pharmacol 1995;50:1841-50.
    • (1995) Biochem Pharmacol , vol.50 , pp. 1841-1850
    • Gelboin, H.V.1    Krausz, K.W.2    Goldfarb, I.3
  • 17
    • 0032525032 scopus 로고    scopus 로고
    • Inhibitory monoclonal antibody to human cytochrome P450 2B6
    • Yang TJ, Krausz KW, Shou M, et al. Inhibitory monoclonal antibody to human cytochrome P450 2B6. Biochem Pharmacol 1998;55:1633-40.
    • (1998) Biochem Pharmacol , vol.55 , pp. 1633-1640
    • Yang, T.J.1    Krausz, K.W.2    Shou, M.3
  • 18
    • 0031717524 scopus 로고    scopus 로고
    • Inhibitory monoclonal antibodies to human cytochrome P450 1A2: Analysis of phenacetin O-deethylation in human liver
    • Yang TJ, Sai Y, Krausz KW, Gonzalez FJ, Gelboin HV. Inhibitory monoclonal antibodies to human cytochrome P450 1A2: analysis of phenacetin O-deethylation in human liver. Pharmacogenetics 1998;8:375-82.
    • (1998) Pharmacogenetics , vol.8 , pp. 375-382
    • Yang, T.J.1    Sai, Y.2    Krausz, K.W.3    Gonzalez, F.J.4    Gelboin, H.V.5
  • 20
    • 0022998708 scopus 로고
    • Characterization of rat and human liver microsomal cytochrome P450 forms involved in nifedipine oxidation, a prototype for genetic polymorphism in oxidative drug metabolism
    • Guengerich FP, Martin MV, Beaune PH, Kremers P, Wolff T, Waxman DJ. Characterization of rat and human liver microsomal cytochrome P450 forms involved in nifedipine oxidation, a prototype for genetic polymorphism in oxidative drug metabolism. J Biol Chem 1986;261:5051-60.
    • (1986) J Biol Chem , vol.261 , pp. 5051-5060
    • Guengerich, F.P.1    Martin, M.V.2    Beaune, P.H.3    Kremers, P.4    Wolff, T.5    Waxman, D.J.6
  • 21
    • 0033567453 scopus 로고    scopus 로고
    • Determination of submicromolar concentrations of formaldehyde by liquid chromatography
    • Jones SB, Terry CM, Lister TE, Johnson DC. Determination of submicromolar concentrations of formaldehyde by liquid chromatography. Anal Chem 1999;71:4030-3.
    • (1999) Anal Chem , vol.71 , pp. 4030-4033
    • Jones, S.B.1    Terry, C.M.2    Lister, T.E.3    Johnson, D.C.4
  • 22
    • 0028858960 scopus 로고
    • Cytochrome P450 inhibitors. Evaluation of specificities in the in vitro metabolism of therapeutic agents by human liver microsomes
    • Newton DJ, Wang RW, Lu AY. Cytochrome P450 inhibitors. Evaluation of specificities in the in vitro metabolism of therapeutic agents by human liver microsomes. Drug Metab Dispos 1995;23:154-8.
    • (1995) Drug Metab Dispos , vol.23 , pp. 154-158
    • Newton, D.J.1    Wang, R.W.2    Lu, A.Y.3
  • 23
    • 0030056594 scopus 로고    scopus 로고
    • Specificity of substrate and inhibitor probes for cytochrome P450s: Evaluation of in vitro metabolism using cDNA-expressed human P450s and human liver microsomes
    • Ono S, Hatanaka T, Hotta H, Satoh T, Gonzalez FJ, Tsutsui M. Specificity of substrate and inhibitor probes for cytochrome P450s: evaluation of in vitro metabolism using cDNA-expressed human P450s and human liver microsomes. Xenobiotica 1996;26:681-93.
    • (1996) Xenobiotica , vol.26 , pp. 681-693
    • Ono, S.1    Hatanaka, T.2    Hotta, H.3    Satoh, T.4    Gonzalez, F.J.5    Tsutsui, M.6
  • 24
    • 0031921010 scopus 로고    scopus 로고
    • Evaluation of the selectivity of in vitro probes and suitability of organic solvents for the measurement of human cytochrome P450 monooxygenase activities
    • Hickman D, Wang JP, Wang Y, Unadkat JD. Evaluation of the selectivity of In vitro probes and suitability of organic solvents for the measurement of human cytochrome P450 monooxygenase activities. Drug Metab Dispos 1998;26:207-15.
    • (1998) Drug Metab Dispos , vol.26 , pp. 207-215
    • Hickman, D.1    Wang, J.P.2    Wang, Y.3    Unadkat, J.D.4
  • 25
    • 0030430033 scopus 로고    scopus 로고
    • Cytochrome P450 isoform inhibitors as a tool for the investigation of metabolic reactions catalyzed by human liver microsomes
    • Bourrie M, Meunier V, Berger Y, Fabre G. Cytochrome P450 isoform inhibitors as a tool for the investigation of metabolic reactions catalyzed by human liver microsomes. J Pharmacol Exp Ther 1996;277:321-32.
    • (1996) J Pharmacol Exp Ther , vol.277 , pp. 321-332
    • Bourrie, M.1    Meunier, V.2    Berger, Y.3    Fabre, G.4
  • 26
    • 0025341331 scopus 로고
    • New colorimetric cytotoxicity assay for anticancer-drug screening
    • Skehan P, Storeng R, Scudiero D, et al. New colorimetric cytotoxicity assay for anticancer-drug screening. J Natl Cancer Inst 1990;82:1107-12.
    • (1990) J Natl Cancer Inst , vol.82 , pp. 1107-1112
    • Skehan, P.1    Storeng, R.2    Scudiero, D.3
  • 27
    • 0028307539 scopus 로고
    • Activation of CYP3A4: Evidence for the simultaneous binding of two substrates in a cytochrome P450 active site
    • Shou M, Grogan J, Mancewicz JA, et al. Activation of CYP3A4: evidence for the simultaneous binding of two substrates in a cytochrome P450 active site. Biochemistry 1994;33:6450-5.
    • (1994) Biochemistry , vol.33 , pp. 6450-6455
    • Shou, M.1    Grogan, J.2    Mancewicz, J.A.3
  • 28
  • 29
    • 0034055659 scopus 로고    scopus 로고
    • Bcl-2 phosphorylation in a human breast carcinoma xenograft: A common event in response to effective DNA-damaging drugs
    • Pratesi G, Polizzi D, Perego P, Dal Bo L, Zunino F. Bcl-2 phosphorylation in a human breast carcinoma xenograft: a common event in response to effective DNA-damaging drugs. Biochem Pharmacol 2000;60:77-82.
    • (2000) Biochem Pharmacol , vol.60 , pp. 77-82
    • Pratesi, G.1    Polizzi, D.2    Perego, P.3    Dal Bo, L.4    Zunino, F.5
  • 30
    • 0028114740 scopus 로고
    • Use of in vitro human metabolism studies in drug development. An industrial perspective
    • Rodrigues AD. Use of in vitro human metabolism studies in drug development. An industrial perspective. Biochem Pharmacol 1994;48:2147-56.
    • (1994) Biochem Pharmacol , vol.48 , pp. 2147-2156
    • Rodrigues, A.D.1
  • 31
    • 0037379318 scopus 로고    scopus 로고
    • Cytochrome P450 in vitro reaction phenotyping: A re-evaluation of approaches used for P450 isoform identification
    • Lu AY, Wang RW, Lin JH. Cytochrome P450 in vitro reaction phenotyping: a re-evaluation of approaches used for P450 isoform identification. Drug Metab Dispos 2003;31:345-50.
    • (2003) Drug Metab Dispos , vol.31 , pp. 345-350
    • Lu, A.Y.1    Wang, R.W.2    Lin, J.H.3
  • 32
    • 6844255884 scopus 로고    scopus 로고
    • Broad phase II and pharmacokinetic study of methoxy-morpholino doxorubicin (FCE 23762-MMRDX) in non-small-cell lung cancer, renal cancer and other solid tumour patients
    • Bakker M, Droz JP, Hanauske AR, et al. Broad phase II and pharmacokinetic study of methoxy-morpholino doxorubicin (FCE 23762-MMRDX) in non-small-cell lung cancer, renal cancer and other solid tumour patients. Br J Cancer 1998;77:139-46.
    • (1998) Br J Cancer , vol.77 , pp. 139-146
    • Bakker, M.1    Droz, J.P.2    Hanauske, A.R.3
  • 33
    • 0033972141 scopus 로고    scopus 로고
    • A prolonged methoxymorpholino doxorubicin (PNU-152243 or MMRDX) infusion schedule in patients with solid tumours: A phase 1 and pharmacokinetic study
    • Fokkema E, Verweij J, van Oosterom AT, et al. A prolonged methoxymorpholino doxorubicin (PNU-152243 or MMRDX) infusion schedule in patients with solid tumours: a phase 1 and pharmacokinetic study. Br J Cancer 2000;82:767-71.
    • (2000) Br J Cancer , vol.82 , pp. 767-771
    • Fokkema, E.1    Verweij, J.2    Van Oosterom, A.T.3
  • 35
    • 14644395463 scopus 로고    scopus 로고
    • Sensitivity of different drug-resistant cell lines to nemorubicin and its metabolites
    • Geroni C, Marsiglio A, Amboldi N, Ballinari D, Saggioro D, Quintieri L. Sensitivity of different drug-resistant cell lines to nemorubicin and its metabolites. J Chemother 2004;16(Suppl 1): 169.
    • (2004) J Chemother , vol.16 , Issue.SUPPL. 1 , pp. 169
    • Geroni, C.1    Marsiglio, A.2    Amboldi, N.3    Ballinari, D.4    Saggioro, D.5    Quintieri, L.6
  • 36
    • 0032924934 scopus 로고    scopus 로고
    • Cytochrome P450 3A4: Regulation and role in drug metabolism
    • Guengerich FP. Cytochrome P450 3A4: regulation and role in drug metabolism. Annu Rev Pharmacol Toxicol 1999;39:1-17.
    • (1999) Annu Rev Pharmacol Toxicol , vol.39 , pp. 1-17
    • Guengerich, F.P.1
  • 37
    • 0028237729 scopus 로고
    • Interindividual variations in human liver cytochrome P-450 enzymes involved in the oxidation of drugs, carcinogens and toxic chemicals: Studies with liver microsomes of 30 Japanese and 30 Caucasians
    • Shimada T, Yamazaki H, Mimura M, Inui Y, Guengerich FP. Interindividual variations in human liver cytochrome P-450 enzymes involved in the oxidation of drugs, carcinogens and toxic chemicals: studies with liver microsomes of 30 Japanese and 30 Caucasians. J Pharmacol Exp Ther 1994;270:414-23.
    • (1994) J Pharmacol Exp Ther , vol.270 , pp. 414-423
    • Shimada, T.1    Yamazaki, H.2    Mimura, M.3    Inui, Y.4    Guengerich, F.P.5
  • 38
    • 0031445547 scopus 로고    scopus 로고
    • Characterization of interintestinal and intraintestinal variations in human CYP3A-dependent metabolism
    • Paine MF, Khalighi M, Fisher JM, et al. Characterization of interintestinal and intraintestinal variations in human CYP3A-dependent metabolism. J Pharmacol Exp Ther 1997;283:1552-62.
    • (1997) J Pharmacol Exp Ther , vol.283 , pp. 1552-1562
    • Paine, M.F.1    Khalighi, M.2    Fisher, J.M.3
  • 39
    • 0000783041 scopus 로고    scopus 로고
    • Evaluation of the genetic component of variability in CYP3A4 activity: A repeated drug administration method
    • Ozdemir V, Kalowa W, Tang BK, et al. Evaluation of the genetic component of variability in CYP3A4 activity: a repeated drug administration method. Pharmacogenetics 2000;10:373-88.
    • (2000) Pharmacogenetics , vol.10 , pp. 373-388
    • Ozdemir, V.1    Kalowa, W.2    Tang, B.K.3
  • 40
    • 0031794361 scopus 로고    scopus 로고
    • Inhibition and induction of cytochrome P450 and the clinical implications
    • Lin JH, Lu AY. Inhibition and induction of cytochrome P450 and the clinical implications. Clin Pharmacokinet 1998;35:361-90.
    • (1998) Clin Pharmacokinet , vol.35 , pp. 361-390
    • Lin, J.H.1    Lu, A.Y.2
  • 41
    • 0036015562 scopus 로고    scopus 로고
    • Tumour cytochrome P450 and drug activation
    • Patterson LH, Murray GI. Tumour cytochrome P450 and drug activation. Curr Pharm Des 2002;8:1335-47.
    • (2002) Curr Pharm Des , vol.8 , pp. 1335-1347
    • Patterson, L.H.1    Murray, G.I.2
  • 42
    • 0036799144 scopus 로고    scopus 로고
    • Neoadjuvant and adjuvant therapy for resectable hepatocellular carcinoma: Review of the randomised clinical trials
    • Schwartz JD, Schwartz M, Mandeli J, Sung M. Neoadjuvant and adjuvant therapy for resectable hepatocellular carcinoma: review of the randomised clinical trials. Lancet Oncol 2002;3:593-603.
    • (2002) Lancet Oncol , vol.3 , pp. 593-603
    • Schwartz, J.D.1    Schwartz, M.2    Mandeli, J.3    Sung, M.4
  • 43
    • 0037048285 scopus 로고    scopus 로고
    • Expression of paclitaxel-inactivating CYP3A activity in human colorectal cancer: Implications for drug therapy
    • Martinez C, Garcia-Martin E, Pizarro RM, Garcia-Gamito FJ, Agundez JA. Expression of paclitaxel-inactivating CYP3A activity in human colorectal cancer: implications for drug therapy. Br J Cancer 2002;87:681-6.
    • (2002) Br J Cancer , vol.87 , pp. 681-686
    • Martinez, C.1    Garcia-Martin, E.2    Pizarro, R.M.3    Garcia-Gamito, F.J.4    Agundez, J.A.5
  • 45
    • 0033917116 scopus 로고    scopus 로고
    • Detoxication of Vinca alkaloids by human P450 CYP3A4-mediated metabolism: Implications for the development of drug resistance
    • Yao D, Ding S, Burchell B, Wolf CR, Friedberg T. Detoxication of Vinca alkaloids by human P450 CYP3A4-mediated metabolism: implications for the development of drug resistance. J Pharmacol Exp Ther 2000;294:387-95.
    • (2000) J Pharmacol Exp Ther , vol.294 , pp. 387-395
    • Yao, D.1    Ding, S.2    Burchell, B.3    Wolf, C.R.4    Friedberg, T.5
  • 46
    • 0034892379 scopus 로고    scopus 로고
    • Clinical pharmacokinetics and metabolism of irinotecan (CPT-11)
    • Mathijssen RH, van Alphen RJ, Verweij J, et al. Clinical pharmacokinetics and metabolism of irinotecan (CPT-11). Clin Cancer Res 2001;7:2182-94.
    • (2001) Clin Cancer Res , vol.7 , pp. 2182-2194
    • Mathijssen, R.H.1    Van Alphen, R.J.2    Verweij, J.3
  • 47
    • 0032958147 scopus 로고    scopus 로고
    • Use of V79 cells with stably transfected cytochrome P450 cDNAs in studying the metabolism and effects of cytotoxic drugs
    • Philip PA, Ali-Sadat S, Doehmer J, et al. Use of V79 cells with stably transfected cytochrome P450 cDNAs in studying the metabolism and effects of cytotoxic drugs. Cancer Chemother Pharmacol 1999;43:59-67.
    • (1999) Cancer Chemother Pharmacol , vol.43 , pp. 59-67
    • Philip, P.A.1    Ali-Sadat, S.2    Doehmer, J.3


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