Zusammenfassung
Die Anthracycline Adriamycin und Daunomycin gehören zu den wirksamsten Substanzen bei der zytostatischen Chemotherapie maligner Tumoren und Systemerkrankungen [6]. Ihre klinische Anwendbarkeit ist über eine Gesamtdosis von 550 mg/m2 hinaus durch ihre kumulative Kardiotoxizität eingeschränkt [32].
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Literatur
Babson JR, Abell NS, Reed DJ (1981) Protective role of the glutathione redox cycle against adriamycin-mediated toxicity in isolated hepatocytes. Biochem Pharmacol 30:2299–2304
Bachur N, Gordon S, Gee M (1977) Anthracycline antibiotic augmentation of microsomal electron transport and free radical formation. Mol Pharmacol 13:901–910
Bachur NR, Gee MV, Friedman RD (1982) Nuclear catalyzed antibiotic free radical formation. Cancer Res 42:1078–1081
Berlin V, Haseltine WA (1981) Reduction of adriamycin to a semiquinone-free radical by NADPG cytochrome P-450 reductase produces DNA cleavage in a reaction mediated by molecular oxygen. J Biol Chem 256:4747–4756
Billingham ME, Mason JW, Bristow MR, Daniels JR (1978) Anthracycline cardiomyopathy monitored by morphologic changes. Cancer Treat Rep 62:865–872
Blum RH, Carter SK (1974) Adriamycin: A new anticancer drug with significant clinical activity. Ann Intern Med 80:249–259
Breed JGS, Zimmermann ANE, Dormans JAMA, Pinedo HM (1980) Failure of the antioxidant vitamin E to protect against adriamycin-induced cardiotoxicity in the rabbit. Cancer Res 40:2033–2038
Bristow MR et al. (1981) Anthracycline-associated cardiac and renal damage in rabbits. Evidence for mediation by vasoactive substances. Lab Invest 45:157–168
Brown OR, Heitkamp M, Song C-S (1981) Niacin reduces paraquat toxicity in rats. Science 212:1510–1512
Bühner R, Biedert S, Miura D (1980) Experimentelle Untersuchungen zur Klärung der Pathogenese der durch Adriamycin induzierten Kardiomyopathie. Arzneimittel-Forsch 30:1065–1070
Chlebowski RT, Paroly WS, Pugh RP, Hueser J, Jacobs EM, Pajak TF, Bateman JR (1980) Adriamycin given as a weekly schedule without a loading course: Clinically effective with reduced incidence of cardiotoxicity. Cancer Treat Rep 64:47–51
Daugherty JP, Wheat M, Conley S, Cooley E, Vanzant C, Loggins L, Durant JR (1982) Involvement of reactive oxygen species in adriamycin cardiotoxicity. Proc Am Ass Cancer Res 23:171
Di Marco A (1975) Adriamycin: Mode and mechanism of action. Cancer Chemother Rep 3:91–106
Doroshow JH, Locker GY, Baldinger J, Myers CE (1979) The effect of doxorubicin on hepatic and cardiac glutathine. Res Commun Chem Pathol Pharmacol 26:285–295
Doroshow JH, Locker GY, Myers CE (1980) Enzymatic defenses of the mouse heart against reactive oxygen metabolites. Alterations produced by doxorubicin. J Clin Invest 65:128–135
Doroshow JH, Locker GY, Ifrim I, Myers CE (1981) Prevention of doxorubicin cardiac toxicity in the mouse by N-acetic cysteine. J Clin Invest 68:1053–1064
Doroshow JH, Reevers J (1981) Daunomycin-stimulated reactive oxygen metabolism in cardiac sarcosomes. Biochem Pharmacol 30:259–262
Formelli F, Zedeck MS, Stemberg SS, Philips FS (1978) Effects of adriamycin on DNA synthesis in mouse and rat heart. Cancer Res 38:3286–3292
Freeman RW, MacDonald JS, Olson RD, Boerth RC, Oates JA, Harbison RD (1980) Effect of sulfhydryl-containing compounds on the antitumor effects of adriamycin. Toxicol Appl Pharmacol 54:168–175
Fujita K et al. (1982) Reduction of adriamycin toxicity by ascorbate in mice and guinea pigs. Cancer Res 42:309–316
Garbrecht M, Müllerleile P, Hanrath P, Langenstein B, Krüger W (1981) Eine mögliche Prävention der adriamycininduzierten Kardiomyopathie durch Kalziumantagonisten. Beitr Onkol 9:43–48. Karger, Basel
Goodman J, Hochstein P (1977) Generation of free radicals and lipid peroxidation by redox cycUng of adriamycin and daunomycin. Biochem Biophys Res Commun 77:797–803
Guthrie D, Gibson AL (1977) Doxorubicin cardiotoxicity. Possible role of digoxin in its prevention. Br Med J 2:1447–1449
Handa K, Sato S (1975) Generation of free radicals of quinone group-containing anticancer chemicals in an NADPH-microsome system as evidenced by initiation of sulfite oxidation. Gann 66:43–47
Herman E, Ardalan B, Bier C, Waravdekar V, Krop S (1979) Reduction of daunorubicin lethality and myocardial cellular alterations by pretreatment with ICRF-187 in Syrian golden hamsters. Cancer Treat Rep 63:89–92
Hixon SC, Ellis CN, Daugherty JP (1981) Heart mitochondrial DNA synthesis: Preferential inhibition by adriamycin. J Mol Cell Cardiol 13:855–860
Iwamoto Y, Hansen IL, Proter TH, Folkers K (1974) Inhibition of coenzyme Q10-enzymes, succinoxidase and NADH-oxidase by adriamycin and other quinones having antitumor activity. Biochem Biophys Res Commun 58:633–638
Kappus H, Muliawan H, Scheulen ME (1980) In vivo studies on adriamycin-induced lipid peroxidation and effects of ferrous ions. In: Holmstedt B, Lauwerys R, Mercier M, Roberfroid M (eds) Mechanisms of Toxicity and Hazard Evaluation. Elsevier/North-Holland, Amsterdam, pp 635–638
Kappus H, Sies H (1981) Toxic drug effects associated with oxygen metabolism: Redox cycling and lipid peroxidation. Experientia 37:1233–1241
Kishi T, Watanabe T, Folkers K (1976) Bioenergetics in clinical medicine: Prevention by forms of coenzyme Q of the inhibition by adriamycin of coenzyme Q10-enzymes in mitochondria of the myocardium. Proc Natl Acad Sci USA 73:4653–4656
Komiyama T, Kikuchi T, Sugiura Y (1982) Generation of hydroxyl radical by anticancer quinone drugs, carbazilquinone, mitomycin C, aclacinomycin A and adriamycin, in the presence of NADPH-cytochrome P-450 reductase. Biochem Pharmacol 31:3651–3656
Lefrak EA, Pitha J, Rosenheim S, Gottlieb JA (1973) Clinicopathologic analysis of adriamycin cardiotoxicity. Cancer 32:302–314
Legha SS et al. (1982) Reduction of doxorubicin cardiotoxicity by prolonged continuous intravenous infusion. Ann Intern Med 96:133–139
Locker GY, Doroshow JH, Myers CE (1977) Glutathione peroxidase: Its role in adriamycin cardiotoxicity. Proc Am Ass Cancer Res 18:87
Mailer K, Petering DH (1976) Inhibition of oxidative phosphorylation in tumor cells and mitochondria by daunomycin and adriamycin. Biochem Pharmacol 25:2085–2089
Mimnaugh EG, Siddik ZH, Drew R, Sikic BI, Gram TE (1979) The effects of alpha-toco-pherol on the toxicity, disposition and metabolism of adriamycin in mice. Toxicol Appl Pharmacol 49:119–126
Momparler RL, Karon M, Siegel SE, Avila F (1976) Effect of adriamycin on DNA, RNA and protein synthesis in cell-free system and intact cells. Cancer Res 36:2891–2895
Muliawan H, Scheuten ME, Kappus H (1980) Acute adriamycin treatment of rats does not increase ethane expiration. Res Commun Chem Pathol Pharmacol 30:509–519
Muliawan H, Scheuten ME, Kappus H (1982) Adriamycin stimulates only the iron-induced, NADPH-dependent microsomal alkane formation. Biochem Pharmacol 31: 3147–3150
Myers CE (persönliche Mitteilung)
Myers CE (1982) The role of free radical damage in the genesis of doxorubicin cardiac toxicity. In: Muggia FM, Young CW, Carter SK (eds) Anthracycline Antibiotics in Cancer Therapy. Developments in Oncology 10:297–305. Martinus Nijhoff, The Hague
Myers CE, McGuire WP, Liss RH, Ifrim I, Grotzinger K, Young RC (1977) Adriamycm: The role of lipid peroxidation in cardiac toxicity and tumor response. Science 197:165–167
Myers CE, McGuire WP, Young RC (1976) Adriamycin: Amelioration of toxicity by alpha-tocopherol. Cancer Treat Rep 60:961–962
Newman RA, Hacker MP, Krakoff IH (1981) Amelioration of adriamycin and daunorubicin myocardial toxicity by adenosine. Cancer Res 41:3483–3488
Olson HM, Young DM, Prieur DJ, Leroy AF, Reagan R (1974) Electrolyte and morphologic alterations of myocardium in adriamycin-treated rabbits. Am J Pathol 77:439–450
Olson RD, MacDonald JS, Harbison RD, van Boxtel CJ, Boerth RC, Slonin AE, Oates JA (1977) Altered myocardial glutathione levels: A possible mechanism of adriamycin toxicity. Fed Proc 36:303
Olson RD et al. (1980) Regulatory role of glutathione and soluble sulfhydryl groups in the toxicity of adriamycin. J Pharmacol Exp Ther 215:450–454
Paul C, Lönnqvist B, Gahrton G, Lockner D, Peterson C (1981) Reducing the cardiotoxicity of anthracyclines by complex-binding to DNA: Report of three cases. Cancer 48:1531–1534
Prestayko AW, Duvernay VH, Long BH, Crooke ST (1982) Effects of anthracyclines on macromolecules and their syntheses. In: Muggia FM, Young CW, Carter SK (eds) Anthracycline Antibiotics in Cancer Therapy. Developments in Oncology 10:117–124. Martinus Nijhoff, The Hague
Rahman A, More N, Schein PS (1982) Doxorubicin-induced chronic cardiotoxicity and its protection by liposomal administration. Cancer Res 42:1817–1825
Revis NW, Marusic N (1978) Glutathione peroxidase activity and selenium concentration in the hearts of doxorubicin-treated rabbits. J Mol Cell Cardiol 10:945–951
Ross W (1980) Adriamycin-induced DNA double strand breaks. Proc Am Ass Cancer Res 21:274
Scheuten ME (1981) Biochemische Ursachen der kumulativen Anthracyclin-Kardiotoxizität — Ansatzpunkte für eine kardioprotektive Begleittherapie? Beitr Onkol 9:64–75. Karger, Basel
Scheuten ME, Kappus H (1982) Metabolie activation of adriamycin by NADPH-cytochrome P-450 reductase, rat Hver and heart microsomes and covalent protein binding of metabolites. In: Snyder R et al. (eds) Biological Reactive Intermediates II. Advances in Experimental Medicine and Biology 136:471–485. Plenum, New York
Scheuten ME, Kappus H, Nienhaus A, Schmidt CG (1982) Covalent protein binding of reactive adriamycin metabolites in rat liver and rat heart microsomes. J Cancer Res Clin Oncol 103:39–48
Scheuten ME, Muliawan H, Kappus H (1982) The rote of acute lipid peroxidation m doxorubicin cardiotoxicity. In: Muggia FM, Young CW, Carter SK (eds) Anthracycline Antibiotics in Cancer Therapy. Developments in Oncology 10:159–164. Martinus Nijhoff, The Hague
Scheuten ME, Niederle N, Seeber S (1980) Ergebnisse einer klinischen Phase II-Studie von Ifosfamid bei therapiefraktären malignen Erkrankungen. Vergleich der uroprotektiven Wirkung von Uromitexan ® mit forcierter Diurese und Alkalisierung des Urins. Beitr Onkol 5:40–47. Karger, Basel
Scheuten ME, Schmitt-Gräff A, Thyssen D (im Druck) Niacin, isocitrate and N-acetylcysteine — potential cardioprotectors in the course of doxorubicin-therapy. Verh Dtsch Krebs- Ges 4
Sinha BK, Sik RH (1980) Binding of (14C)-adriamycin to cellular macromolecules in vitro. Biochem Pharmacol 29:1867–1868
Taylor D, Hochstein P (1978) Inhibition by adriamycin of metmyoglobin reductase from beef heart. Biochem Pharmacol 27:2079–2082
Tritton TR, Yee G (1982) The anticancer agent adriamycin can be actively cytotoxic without entering cells. Science 217:249–250
Trouet A, Deprez-de Campeneere D, de Duve C (1972) Chemotherapy through lysosomes with DNA-daunorubicin complex. Nature 239:110–112
Vleet JF van, Ferrans VJ (1980) Evaluation of vitamin E and selenium protection against chronic adriamycin toxicity in rabbits. Cancer Treat Rep 64:315–317
Wang G, Finch MD, Trevan D, Hellmann K (1981) Reduction of daunomycin toxicity by razoxane. Br J Cancer 43:871–877
Wang Y-M, Madanat FF, Kimball JC, Gleiser CA, Ali MK, Kaufman MW, van Eys J (1980) Effect of vitamin E against adriamycin-induced toxicity in rabbits. Cancer Res 40:1022–1027
Weiss AJ, Metier GE, Fletcher WS, Wilson WL, Grage TB, Ramirez G (1976) Studies on adriamycin using a weekly regimen demonstrating its clinical effectiveness and lack of cardiac toxicity. Cancer Treat Rep 60:813–822
Yamanaka N, Kato T, Nishida K, Fujikawa T, Fukushima M, Ota K (1979) Elevation of serum Hpid peroxide level associated with doxorubicin toxicity and its amelioration by (dl)-alpha-tocopherol acetate or coenzyme Q10 in mouse. Cancer Chemother Pharmacol 3:223–227
Yasumi M, Minaga T, Takamura K, Kizu A, Ijichi H (1980) Inhibition of cardiac NADP-linked isocitrate dehydrogenase by adriamycin. Biochem Biophys Res Commun 93: 631–636
Zak R (1973) Cell proliferation during cardiac growth. Am J Cardiol 31:211–219
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Scheulen, M.E. (1983). Kumulative Anthracyclin-Kardiotoxizität. Möglichkeiten für eine kardioselektive Protektion durch Begleittherapie mit Isozitrat und Niacin. In: Schmidt, C.G. (eds) Aktuelle Probleme der Hämatologie und internistischen Onkologie. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-68998-7_11
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