Zusammenfassung
Die Krebszelle entsteht durch eine irreversible Abweichung aus normalen Zellen. Die Einzelheiten dieses Vorganges sind bisher nicht genügend bekannt, jedoch kommt ihm am ehesten der Charakter eines Defektes zu, durch den die Krebszellen zunehmend unabhängig von normalen Regulationen werden. Sie sind den geschlossenen Regelsystemen (feed back), die ebenso wie die bekannten physiologischen Regulationen auch das Wachstum kontrollieren werden, nicht länger unterworfen. Krebszellen existieren somit nicht mehr als Untereinheiten eines Organs oder Gewebes, sondern als selbständige Population einer neuen Zellart. Im Hinblick auf die genetische Abhängigkeit biochemischer Reaktionen ist es möglich, daß die Tumorzellen in ihren Eigenschaften genetisch fixiert sind (246, 456), jedoch sind die Kenntnisse über diesen Aspekt der Cancerogenese noch gering. Die krebsartige Entartung der Zelle geschieht nach experimenteller Erfahrung langsam und schrittweise, in der Regel nicht sprunghaft. Sie ist möglicherweise in den ersten Stadien noch reversibel. Selbst bei eingetretener Cancerisierung kann anfänglich noch eine Abhängigkeit von den normalen Regulationen des Organismus bestehen. Dies wird deutlich bei den sog. „hormonabhängigen“ Geschwülsten, die — wie das Prostata- und Mamma-Carcinom — mit hormonal wirksamen Eingriffen behandelt werden können (175, 176). Die Hormonabhängigkeit dieser Neoplasmen geht jedoch früher oder später verloren, ohne daß es gelungen wäre, morphologische oder cytologische Kriterien für diesen Vorgang der Progression der Malignität (114, 267) zu entdecken.
Die in diesem Referat zitierten eigenen Arbeiten wurden mit dankenswerter Unterstützung des Kultusministeriums des Landes Nordrhein/Westfalen, Düsseldorf, durchgeführt.
Herrn Prof. Dr. E. Lehnartz in Verehrung zum 65. Geburtstag gewidmet.
Referat, auszugsweise gehalten auf der Tagung der Gesellschaft zur Bekämpfung der Krebskrankheiten, Düsseldorf 1. u. 2.12.1962.
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Literatur
Abraham, E. P., and G. G. F. Newton: Chemistry and classification of antibiotics. Brit. med. Bull. 16, 3 (1960).
Abrams, R., and M. Bentley: Biosynthesis of nucleic acid purines. III. Guanosine 5′- phosphate formation from xanthosine 5′-phosphate and L-glutamine. Arch. Biochim. 79, 91 (1959).
Albrich, E., U. P. Hefel: Zur Behandlung eines multiplen Myeloms (Gamma-Plasmo- cytom) mit Actinomycin C. (Sanamycin). Med. Klin. 51, 469 (1956).
Alder, A., U. F. Zbinden: Zur Therapie des Lymphogranuloms. (Morbus Hodgkin). Schweiz, med. Wschr. 83, 924 (1953).
Anderson, E. P., B. Levenberg and L. W. Law: Purine biosynthesis in azaserine- sensitive and-resistant lines of the mouse plasma cell neoplasma 70429. Fed. Proc. 16, 145 (1957).
Anderson, E. P., and J. A. Jacquez: Azaserine resistance in a plasmacell neoplasm without change in active transport of the inhibitor. Cancer Res. 22, 27 (1962).
Back, N., R. R. Shields and A. E. Munson: The effect of the antibiotic spiramycin in a spectrum of transplantable animal tissues. Antibiot. and Chemother. 11, 652 (1961).
Back, N, and E. Feltz: Zitiert bei N. Back, R. R. Shields and A. E. Munson: Antibiot. and Chemother. 11, 652 (1961).
Back, N, J. L. Ambrus, R. K. Ausman, L. Stutzman, J. E. Sokal and H. Velasco: Studies with intravenous spiramycin, an antibiotic with potential antitumour effect. 8. Internat. Krebscongress, Moskau 1962, S. 366.
Baker, B. R.: Potential anti-cancer agents. II. A proposed mechanism for the anti-cancer action of L-azaserine and 6-diazo-5-oxo-L-norleucine. Biochem. Pharmacol. 2, 161 (1959).
Balassa, J.: Action de la mitomycine C sur la transformation du pneumocoque. Ann. Inst. Pasteur 102, 547 (1962).
Barker, S. A., J. A. Bassham, M. Calvin and U. A. Quarck: Sites of azaserine inhibition during photo-synthesis by scenedesmus. J. Amer. ehem. Soc. 78, 4632 (1956).
Bartz, Q. R., C. C. Elder, R. P. Frohardt, S. A. Fusari, T. H. Haskell, D. W. Johannessen and A. Ryder: Isolation and characterization of azaserine. Nature (Lond.) 173, 72 (1954).
Bases, R. E.: Modification of the radiation response determined by single-cell technics: Actinomycin D. Cancer Res. 19, 1233 (1959).
Begemann, H.: Clinical experience with actinomvcin c. Ann. N. Y. Acad. Sci. 89, 454 (1960).
Begemann, H. Que peut-on attendre de l’actinomycine dans les maladies cancereuses ou paracancereuses ? J. Therap. Paris 1955.
Benazet, F., and M. Du Bost: Apparent paradox of antimicrobial activity of spiramycin: In: H. Welch and F. Marti-Ibanez: Antibiot. Ann. 1958–59, N. Y. Medical Encyclopedia Inc. 1959, S. 211.
Bennett, L. L. jr., F. M. Schabel jr. and H. E. Skipper: Studies on the mode of action of azaserine. Arch. Biochim. 64, 423 (1956).
Ben-Porat, T., M. Reissig and A. S. Kaplan: Effect of mitomycin C on the synthesis of infective virus and deoxyribonucleic acid in Pseudorabies virus-infected rabbit kidney cells. Nature (Lond.) 190, 33 (1961).
Bentley, H. R., K. G. Cunningham and F. S. Spring: Cordycepin, a metabolic product from cultures of cordyceps militaris (Linn) Link part II. The structure of cordycepin. J. chem. Soc. 1951, 2301.
Bertino, J. R., B. W. Gabrio and F. M. Huennekens: Dihydrofolic reductase in human leucemic leucocytes. Biochim. biophys. Acta Res. Commun. 3, 461 (1961).
Bertino, J. R, F. M. Huennekens and B. W. Gabrio: Increased activity of leukocyte dihydrofolic reductase in amethopterine-treated patients. Clin. Res. 9, 157 (1961).
Bertrand-Fontaine, P., J. Mallarme, J. Schneider et J. Debray: Essais de traitement de la maladie de Hodgkin par l’actinomycine. Presse méd. 62, 737 (1954).
Bierling, R.: Die Wirkung von Actinomycinen auf menschliche Gewebe in vitro. Z. Krebsforsch. 63, 519 (1960).
Bloemendal, H., U. Z. Littauer and V. Daniel: Transfer of soluble polynucleotides to microsomal RNA. Biochim. biophys. Acta (Amst.) 51, 66 (1961).
Bloemendal, and L. Bosch: Requirements and tentative mechanism for the interaction between soluble and microsomal ribonucleic acid in rat liver. Biochim. biophys. Acta. (Amst.) 55, 261 (1962).
Bollag, W., U. A. F. Esselier: Erfahrungen mit Actinomycin C. Schweiz, med. Wschr. 84, 1174 (1954).
Börnstein, R., U. F. Stein: Anatomische Heilung einer Lymphogranulomatose nach Actinomycintherapie. Ärztl. Wschr. 9, 896 (1954).
Bosch, L., and H. Bloemendal: The effect of puromycin on nucleotide and amino acid transfer from soluble ribonucleic acid to the microsomes. Biochim. biophys. Acta (Amst.) 51, 613 (1961).
Bradner, W. T., D. A. Clarke and C. C. Stock: Stimulation of host defense against experimental cancer. I. Zymosan and sarcoma 180 in mice. Cancer Res. 18, 347 (1958).
Bradner, and K. Sugiura: Actinogan: A new antitumor agent obtained from streptomyces. II. Studies in the sarcoma 180 and in a tumor spectrum. Cancer Res. 22, 167 (1962).
Brazhnikova, M. G., YE. B. Kruglyak, I. N. Koysharova, N. V. Konstantinova and V. V. Proshlyakova: New methodes of cancer treatment (antibiotics, chemotherapy). The production and chemical properties of the antitumor antibiotic olivomycin. 8. Internat. Krebscongress, Moskau 1962, S. 364.
Brockman, R. W., C. Sparks, T. J. Hutchison and H. E. Skipper: A mechanism of resistance to 8-azaguanine. I. Microbiological studies on the metabolism of purines and 8-azapurines. Cancer Res. 19, 177 (1959).
M. S. Simpson and H. E. Skipper: Decreased ribonucleotide pyrophosphorylase activity of streptococcus faecalis and L 1210 leukemia resistant to purine antagonists. Biochem. Pharmacol. 2, 77 (1959).
M. S. Simpson A mechanism of resistance to 6-mercaptopurine: metabolism of hypoxanthine and 6-mercaptopurine by sensitive and resistant neoplasms. Cancer Res. 20, 643 (1960).
Brockmann, H., u. M. Grtjbhofer: Actinomycin; Zur Kenntnis des Actinomycin C. Naturwissenschaften 36, 376 (1949); 37, 494 (1950).
Brockmann, H., Chemie und Biologie der Actinomycine. Angew. Chem. 66, 1 (1954) und H. Brockmann, A. Bohne und H. Friedrich: Zur Entstehungsgeschichte des H.B.F. 386, Actinomycin C Bayer. Dtsch. med. Wschr. 79, 437 (1954).
Brockmann, H, u. H. Muxfeldt: Konstitution und Synthese des Actinomycin. Angew. Chem. 68, 67 (1956).
Brockmann, H, u. B. Franck: Hydrierende Acetylierung von Actinomycinen. Aufspaltung der Actinomycine zu Actinomycinsäuren. Angew. Chem. 68, 68 (1956).
Brockmann, H, u. H. Muxfeldt: Konstitution und Synthese des Actinomvcin-Chromophors. Angew. Chem. 68, 69 (1956).
Brockmann, H, G. Bohnsack, B. Franck, H. Grone, H. Muxfeldt u. C. Süling: Bilanz der Actinomycin C3-Abbauprodukte. Angew. Chem. 68, 70 (1956).
Brockmann, H, u. J. H. Manegold: Überführung von Actinomycin X2 in Actinomycin XJ. Natur-wissenschaften 45, 310 (1958).
Brockmann, H, u. H. Muxfeldt: Konstitution und Synthese des Actinomycin-Chromophors. Chem. Ber. 91, 1242 (1958).
Brockmann, H, G. Pampus U. J. H. Manegold: ActinomycinX0ß; zur Systematik und Nomenklatur der Actinomycine. Chem. Ber. 92, 1294 (1959).
Brockmann, H, Structural differences of the actinomycins and their derivatives. Ann. N. Y. Acad. Sci. 89, 323 (1960).
Brunsch, K. H., U. J. Nevinny-Stickel: Über die Lymphogranulomatose im Bereich der Weiblichen Geschlechtsorgane. Arch. Gynäk. 188, 215 (1957).
Buchanan, J. M.: The effect of azaserine and 6-diazo-5-oxo-L-norleucine on the bio-synthesis of inosine acid “de novo”. Tex. Rep. Biol. Med. 15, 148 (1957).
Buchanan, J. M., Enzymatic synthesis of purine nucleotides. Harvey Lect. 54, 104 (1958/59).
Bullock, E., and A. W. Johnson: Actinomycin V. The structure of actinomycin D. J. chem. Soc. 1957, 3280.
Burchenal, J. H., H. F. Oettgen, J. A. Reppert and V. Coley: The effect of actinomycins and their derivatives on a spectrum of transplanted mouse leukemia. Ann. N. Y. Acad. Sci. 89, 399 (1960).
Businco, L.: Actinomycin C, anaphylaxie allergie. Presse med. 1955, 1687.
Butenandt, A., W. Weidel U. E. Becker: Kynurenin als Augenpigmentbildung auslösendes Agens bei Insekten. Naturwissenschaften 28, 63 (1940).
Butenandt, A. Biochemische Untersuchungen zur Wirkungsweise der Erbfaktoren. Angew. Chem. 61, 262 (1949).
Butenandt, A U. Schiedt, E. Biekert u. P. Kornmann: Über Ommochrome. I. Mitt.: Isolierung von Xanthommatin, Rhodommatin und Ommatin C aus den Schlupfsekreten von Vanessa utricae. Justus Liebigs Ann. Chem. 586, 217 (1954).
Butenandt, A Biochemische Beiträge zur Insektenphysiologie. Gesellschaft Physiol. Chem. 20–22.9.1954 (Kiel).
Butenandt, A., U. Schiedt U. E. Biekert: Über Ommochrome. II. Mitt. Alkalischer und fermentati- ver Abbau von Xanthommatin und Rhodommatin. Alkalischer Abbau der Kynurenin- Seitenkette. Justus Liebigs Ann. Chem. 588, 229 (1954).
Butenandt, A. U. G. Neubert: Über Ommochrome. V. Mitt.: Xanthommatin, ein Augenfarbstoff der Schmeißfliege, Calciphora erythrocephala. Hoppe-Seylers Z. physiol. Chem. 301, 109 (1955).
Butenandt, u. R. Beckmann: Über Ommochrome. VI. Mitt.: Zur Genese von Rhodommatin und Ommatin C. Hoppe-Seylers Z. physiol. Chem. 301, 115 (1955).
Butenandt, U.,U. Schiedt, E. Biekert, R. Jan und T. Cromartie: Über Ommochrome. IV. Mitt.: Konstitution des Xanthommatins. Justus Liebigs Ann. Chem. 590, 75 (1955).
Butenandt, U., E. Biekert U. B. Linzen: Über Ommochrome. VII. Mitt. Modellversuche zur Bildung des Xanthommatins in vivo. Hoppe-Seylers Z. physiol. Chem. 305, 284 (1956).
Butenandt, U., R. Beckmann: Über Ommochrome. XII. Mitt.: Reindarstellung von Rhodommatin und Ommatin D. Zur Struktur des Rhodommatins. Justus Liebigs Ann. Chem. 607, 207 (1957).
Butenandt, U, R. Beckmann, Wirkstoffe des Insektenreiches. Naturwissenschaften 46, 461 (1959).
Caputo, A., B. Giovanella and R. Giuliano: Antitumoral action of new sarcomycin derivatives. Nature (Lond.) 190, 819 (1961).
Caputo, A., M. Brunori and R. Giuliano: Antitumoral action of new sarcomycin derivatives. I. Importance of ethyl radical and substituted methylene groups. Cancer Res. 21, 1499 (1961).
Clarke, D. A., F. S. Philips, C. C. Stock, G. B. Ellion and G. H. Hitchings: Combined chemotherapy of mouse sarcoma 180: Azaserine and 6-mercaptopurine. Abstr. Amer. Chem. Soc. p. 12–14 (1954).
Clarke, D. A., H. C. Reilly and C. C. Stock: 6-diazo-5-oxo-L-norleucine a new tumor inhibitory substance. Effects on mouse sarcoma 180. Abstr. 12 M, 129th Meeting Amer. chem. Soc. 1956.
Clarke, D. A., H. C. Reilly and C. C. Stock A comparative studie of 6-diazo-5-oxo-L-norleucine and o-diazoacetyl-L-serine on sarcoma 180. Proc. Amer. Ass. Cancer Res. 2, 100 (1956).
Clarke, D. A., H. C. Reilly and C. C. Stock Comparative studies of 6-diazo-5-oxo-L-norleucine and o-diazoacetyl-L-serine on sarcoma 180. Antibiot. and Chemother. 7, 653 (1957).
Cobb, J. P., and D. G. Walker: Effect of actinomycin D on tissue cultures of normal and neoplastic cells. J. Nat. Cancer Inst. 21, 263 (1958).
Clarke, D. A., H. C. Reilly and C. C. Stock, Studies on human melanoma cells in tissue culture. II. Effect of several cancer chemotherapeutic agents on cytology and growth. 8. Internat, Krebscongress, Moskau 1962, S. 323.
Coffey, G. L., A. B. Hillegas, M. P. Knudsen, H. J. Koepsell, J. E. Oyaas and J. Ehrlich: Azaserine: Microbiological studies. Antibiot. and Chemother. 4, 775 (1954).
Cohen, S. S., and H. Barner: Unbalanced growth in escherichia coli. Proc. nat. Acad. Sci. (Wash.) 40, 385 (1954).
Colebatch, J. H., R. Howard, A. L. Williams, A. L. Clark and G. R. Kurrle: Actinomycin D therapy for Wilms tumour. 8. Internat. Krebscongress, Moskau 1962, S. 347.
Colsky, J., C. G. Escher, A. Evans, A. Mitus, M. D. Li, S. Roat, R. D. Sullivan, M. P. Sykes and C. T. C. Tan: Preliminary clinical pharmacology of mitomycin C. Proc. Amer. Ass. Cancer Res. 3, 13 (1959).
Cornman, I.: Survival of normal cells in penicillin solutions lethal to malignant cells. Science 99, 247 (1944).
Craveri, R., U. G. V. Veronesi: Wirkung von Actinomycin auf die Mitose. Nature (Lond.) 179, 1306 (1957).
Croizat, P.: Essais thérapeutiques concernant l’actinomycine C. Presse méd. 62, 738 (1954).
Cunningham, K. G., S. A. Hutchinson, W. Manson and F. S. Spring: Cordycepin, a metabolic product from cultures of cordyceps militaris (Linn) Link part I. Isolation and characterization. J. chem. Soc. 1951, 2299.
Dagg, C. P., and D. A. Karnofsky: Teratogenic effects of azaserine on the chick embryo. J. exper. Zool. 130, 555 (1955).
Dalgliesh, C. E., and A. R. Todd: Actinomycin. Nature (Lond.) 164, 830 (1949).
Dalgliesh, C. E., A. W. Johnson, A. R. Todd and L. C. Vining: Actinomycin. I. Amino acid content. J. chem. Soc. 1950, 2946.
D’angio, G. J., S. Farber and C. L. Maddock: Potention of X-ray effects by actinomycin D. Radiology 73, 175 (1959).
Davidson, J. D.: Studies on the mechanism of action of 6-mercaptopurine in sensitive and resistant L 1210 leukemia in vitro. Cancer Res. 20, 225 (1960).
De Boer, C., A. Dietz, N. E. Lummis and G. M. Savage: Porfiromycin, a new antibiotic. I. Discovery and biological activities. Conference on Antimicrobial Agents, October 26–28, 1960, Washington.
De Cort, J., and L. Delcambe: Separation of actinomycin C fractions and experimental evaluation of their carcinolytic and other biological properties. J. nat. Cancer Inst. 19, 1043 (1957).
Dion, H. W., S. A. Fusari, Z. L. Jakubowski, J. G. Zora and Q. R. Bartz: 6-diazo-5- oxo-L-norleucine, a new tumor inhibitory substance. II. Isolation and characterization. J. Amer. Soc. 78, 3075 (1956).
Di Paolo, J. A., G. E. Moore and T. F. Niedbala: Experimental studies with actinomycin D. Cancer Res. 17, 1127 (1957).
Di Paolo, J. A., Experimental evaluation of actinomycin D. Ann. N. Y. Acad. Sci. 89, 408 (1960).
Doerr, W., U. F. Stein: Therapeutisch bedingte Pathomorphose. Münch, med. Wschr. 1954, 660.
Dold, U., M. Mielsch U. H. Holzer: DPN-Gehalt, Nucleinsäure-Gehalt und Zellstruktur von Ascites-Tumorzellen nach Einwirkung alkylierender Cytostatika. Z. Krebsforsch. 65. 139 (1962).
Domagk, G.: Welche Erkenntnisse über den Krebs vermittelt uns die experimentelle Krebsforschung? Münch, med. Wschr. 1952, 1841.
Eble, T. E., M. E. Bergy, C. M. Large, R. R. Herr and W. G. Jackson: Isolation, purification and properties of streptovitacins A and B. Antibiotics Ann. S. 555 ( Medical Encyclopedia N. Y. 1959 ).
Eble, T. E., H. Hoeksema, G. A. Boyack and G. M. Savage: Psicofuranine. I. Discovery, isolation and properties. Antibiot. and Chemother. 9, 419 (1959).
Ehrlich, J., G. L. Coffey, M. W. Fisher, A. B. Hillegas, D. L. Kohberger, H. E. Machamer, W. A. Rightsel and F. R. Roegner: 6-diazo-5-oxo-L-norleucine, a new tumor inhibitory substance. I. Biological studies. Antibiot. and Chemother. 6, 487 (1956).
Eidinoff, M. L., J. E. Knoll, B. Marano and L. Choeng: Pyrimidine studies. I. Effect of DON (6-diazo-5-oxo-L-norleucine) on incorporation of precursors into nucleic acid pyrimidines. Cancer Res. 18, 105 (1958).
Ellison, R. R., D. A. Karnofsky, S. S. Sternberg, M. L. Murphy and J. H. Burchenal: Clinical trials of o-diazoacetyl-L-serine (azaserine) in neoplastic disease. Cancer 7, 801 (1954).
Evans, J. S., G. Mengel, J. Ceru and R. L. Johnston: Biological studies on streptovitacin A, a new antitumora gent. Antibiotics Ann. S. 565 ( Medical Encyclopedia N. Y. 1959 ).
Evans, J. S., and J. E. Gray: Psicofuranine. VI. Antitumor and toxicopathological studies. Antibiot. and Chemother. 9, 675 (1959).
Evans, A. E.: Mitomycin C. Cancer Chemother. Rep. 14, 1 (1961).
Evans, J. S., A. E. Musser and J. E. Gray: Porfiromycin antitumor and toxicopathologic studies. Antibiot. and Chemother. 11, 445 (1961).
Farber, S.: Clinical and biological studies with actinomycins. IN: Amino acids and peptides with antimetabolitic activity. Boston: Little Brown. 1958 — Geigy-Symp. S. 138.
Farber, S., Current clinical and experimental studies in cancer chemotherapy. Unio Internat, contra cancrum. Tokyo p. 42 (1960).
Farber, S., G. D’angio, A. Evans and A. Mitus: Clinical studies of actinomycin D with special reference to Wilms tumor in children. Conference on the actinomycins and their importance in the treatment of tumors in animals and man. Ann. N. Y. Acad. Sci. 89, 421 (1960).
Fernandes, J. F., G. A. Le Page and A. Lindner: The influence of azaserine and 6-mercaptopurine on the in vivo metabolism of ascites tumor cells. Cancer Res. 16, 154 (1956).
Field, J. B., F. Costa, A. Boryczka and L. I. Sekely: Experimental evaluation of the anticarcinogenic activity of a new antibiotic, actinomycin C. Antibiot. Ann. 1954/55, 842.
Field, J. B., F. Costa, A. Boryczka: Origin of a new antitumor agent, streptovitacin. Antibiot. Ann. S. 547 ( Medical Encyclopedia N. Y. 1959 ).
Field, J. B. A. Mireless, H. R. Pachl, L. Bascoy, L. Cano and W. K. Bullock: Experimental evaluation of a new antitumor agent, streptovitacin A. Antibiot. Ann. S. 572 ( Medical Encyclopedia N. Y. 1959 ).
E. C. Dolendo, F. Costa, A. Boryczka, H. Pachl, L. Bascoy, L. Cano and W. K. Bullock: A new antitumor agent, streptovitacin A. Proc. A.Er. Ass. Cancer Res. 3, 19 (1959).
E. C. Dolendo, C. G. Smith and J. E. Grady: Studies on dosage regimens. Blood levels and urine levels with streptovitacin A. Proc. A.Er. Ass. Cancer Res. 3, 109 (1960).
E. Dolendo and A. Mireless: Preliminary canine and clinical evaluation of a new antitumor agent, streptovitacin A. Clin. Res. 8, 134 (1960).
Fischer, G. A.: Nutritional and amethopterin-resistant characteristics of leukemic clones. Cancer Res. 19, 372 (1959).
Fischer, G. A.: Increased levels of folic acid reductase as a mechanism of resistance to amethopterin in leukemic cells. Biochem. Pharmacol. 7, 75 (1961).
Fleischhacker, H., U. A. Stacher: Wert und Wirkung der Zytostatika bei malignen lymphatischen Systemerkrankungen. Wien. Z. inn. Med. 43, 200 (1962).
Foulds, L.: Neoplastic development. Johns Hopk. Hosp. Bull. 1958, 680.
Frank, W., and A. E. Osterberg: Mitomycin C, the evaluation of the japanese reports. Cancer Chemother. Rep. 9, 114 (1960).
Friederici, L.: Untersuchungen über den Einfluß des Actinomycin C (Sanamycin) auf das Blut und die blutbildenden Organe des Kaninchens sowie auf Knochenmarkskulturen. Z. Krebsforsch. 60, 553 (1955).
Fusari, S. A., R. P. Frohardt, A. Ryder, T. H. Haskell, D. W. Johannessen, C. C. Elder and Q. R. Bartz: Azaserine, a new tumor-inhibitory substance. Isolation and characterization. J. Amer. ehem. Soc. 76, 2878 (1954).
Fusari, S. A., T. H. Haskell, R. P. Frohardt and Q. R. Bartz: Azaserine, a new tumor-inhibitory substance. Structural studies. J. Amer. chem. Soc. 76, 2881 (1954).
Garattini, S., V. Costa, B. Murelli, V. Palma e N. Vegeto: G. ital. Chemioter. 3, 498 (1956).
Gasperini, G.: Recherches morphologiques et biologiques sur un microorganisme du l’atmosphère. Ann. Microgr. 10, 449 (1890).
Gauze, G. F., R. S. Ukholina and M. A. Sveshnikova: Olivomycin, an antitumor antibiotic, its production and the mechanism of action. 8. Internat. Krebscongress, Moskau 1962, S. 363.
Gellhorn, A., and E. Hirschberg: Investigations of diverse systems for cancer chemotherapy screening. Cancer Res. Suppl. Nr. 3 (1955).
Gernez-Rieux, CH., et M. Goudemand: Premiers résultats de l’emploi de l’actinomycine C en thérapeutique. Presse méd. 62, 739 (1954).
Giuliano, R., M. Di Fonzo e A. Ermili: Ricerche chimiche sulla sarcomicina e composti analogli. Nota I. Nuova sintesi dell’ acido ciclopentanon-3-carbossilico. Ann. Chim. 49, 1607 (1959).
e M. Artico: Ricerche chimiche sulla sarcomicina e composti analogli. Nota II. Sintesi délia diidrosarcomicinae délia omodiidrosarcomicina (acido 2-etil-ciclo-pentanon- 3-carbossilico). Ann. Chim. 50, 750 (1960).
Goldberg, I. H.: Ribonucleic acid synthesis in nuclear extracts of mammalian cells grown in suspension culture; effect of ionic strength and surface-active agents. Biochim. biophys. Acta (Amst.) 51, 201 (1961).
Goldberg, I. H, and M. Rabinowitz: Actinomycin D inhibition of deoxyribonucleic acid-dependent synthesis of ribonucleic acid. Science 136, 315 (1962).
Goldin, A., and N. Mantel: The employment of combinations of drugs in the chemotherapy of neoplasma: A review. Cancer Res. 17, 635 (1957).
Goldstein, M. N., I. J. Slotnick and L. J. Journey: In vitro studies with HeLa cell lines sensitive and resistent to actinomycin D. Ann. N. Y. Acad. Sci. 89, 474 (1960).
Gorski, J., Y. Aizawa and G. C. Mueller: Effect of puromycin in vivo on the synthesis of protein, RNA and phospholipides in rat tissue. Arch, biochem. 95, 508 (1961).
Gotts, J. S., and E. G. Gollub: Studies on the action of L-azaserine as an inhibitor of purine biosynthesis. Proc. Amer. Ass. Cancer Res. 2, 111 (1956).
Greenlees, J., and G. A. Le Page: Purine biosynthesis and inhibitors in ascites cell tumors. Cancer Res. 16, 808 (1956).
Gregory, F. J., L. H. Pugh, T. Hata and R. Thielen: The effect of actinomycin D on experimental ascitic tumors in the mouse. Cancer Res. 16, 985 (1956).
Greig-Smith, R.: Contributions to our knowledge of soil fertility: the action of certain microorganisms upon the numbers of bacteria in the soil. Proc. Linnean Soc. N. S. Wales 42, 162 (1917).
Gröner, H.: Zur Chemie der Actinomycine. 4. Nat. Kongress für Chemotherapie. Rom 1956.
Grubhofer, N.: Neue Apparatur zur fraktionierten Gegenstromverteilung zwischen zwei Flüssigkeiten. Chem.-Ing.-Techn. 22, 209 (1950).
Hackethal, C. A., and R. B. Cölbe Y: Preliminary clinical study of streptonigrin in neoplastic disease. Proc. Amer. Ass. Cancer Res. 3, 115 (1960).
Hackmann, CH.: Experimentelle Untersuchungen über die Wirkung von Actinomycin C (HBF 386) bei bösartigen Geschwülsten. Z. Krebsforsch. 58, 607 (1952).
Hackmann, CH.: HBF 386 (Actinomycin C) ein cytostatisch wirksamer Naturstoff. Strahlentherapie 90, 297 (1953).
Hackmann, CH.: Les recherches expérimentales sur le cancer. Rev. Progrès Thérap. 23, 64 (1954).
Hackmann, CH.: Untersuchungen über den Einfluß des Sanamycin (Actinomycin C) auf tierische Organe: Milz, Thymus, Lymphknoten, Nebennieren und Keimdrüsen. Z. Krebsforsch. 60, 250 (1954).
Hackmann, CH.: Stoffwechselprodukte aus Mikroorganismen (Antibiotika) als antineo plastische Wirkstoffe. Dtsch. med. Wschr. 80, 812 (1955).
Hackmann, CH., u. G. Schmidt-Kastner: Über die cytostatische Wirkung verschiedener neuer bio-synthetischer Actinomycine bei experimentellen Tumoren. Z. Krebsforsch. 61, 607 (1957).
Hackmann, CH.: Der zytostatische Effekt antibiotischer Wirkstoffe. Krebsforsch, u. Krebsbekämpf. 3, 333 (1959).
Hackmann, CH.: Berliner Symposium 1959. S. 329. Berlin: Akademie Verlag 1960.
Haensch, R.: Elektrophoretische Serumuntersuchungen bei Lymphogranulomatose - Patienten unter der Sanamycin-Behandlung. Z. Haut- u. Geschl.-Kr. 21, 269 (1956).
Hakala, M. T., S. F. Zakrzewski and C. A. Nichol: Mechanism of resistance to ameth- opterin in sarcoma 180 (S-180) cells in cultures. Proc. Amer. Ass. Cancer Res. 3, 115 (1960).
Hanka, L. J.: Mechanism of action of psicofuranine. J. Bact. 80, 30 (1960).
Hackmann, CH.: Porfiromycin, a new antibiotic. IV. Microbiological assays. Conference on antimicrobial agents. October, 26–28, 1960 Washington.
Hara, T.: Preparation of sarcomycin derivatives. Cancer ehem. Abstr. 1, 4095 (1960).
Harbers, E., and W. Mueller: On the inhibition of RNA synthesis by actinomycin. Biochem. biophys. Res. Commun. 7, 107 (1962).
Hartman, S. C., B. Levenberg and J. M. Buchanan: Involvement of ATP, 5-phos- phoribosylpyrophosphate and L-azaserine in the formation of glycinamide ribotide intermediates in inosinic acid biosynthesis. J. Amer. chem. Soc. 77, 501 (1955).
Hata, T., F. Koga, Y. Sano, K. Kanamori, A. Matsumae, R. Sugawara, T. Hoshi and T. Shima: Carcinophilin, a new tumor inhibiting substance produced by a streptomyces. J. Antibiot. (Tokyo) Ser. A. 7, 107 (1954).
Hata, T., Y. Sano, R. Sugawara, A. Matsumae, K. Kanamori, T. Shima and T. Hoshi: Mitomycin, a new antibiotic from streptomyces. J. Antibiot. (Tokyo) Ser. A 9, 141 (1956).
Hata, T., A. Matsumae, K. Owada and Y. Sano: Studies on the treatment of experimental infections. Chemother. Rev. 4, 295 (1956).
Heckner, F., J. Hamm U. W. Eger: Cytologische Kriterien der Wirkung von Sanamycin. Klin. Wschr. 35, 459 (1957).
Heidelberger, C., A. Ghobar, R. K. Baker and L. K. Mukherjee: Studies on fluorinated pyrimidines. X. In vivo studies on tumor resistance. Cancer Res. 20, 897 (1960).
Henderson, J. F., and I. G. Junga: Inhibition of ascites tumor growth by 4-amino- pyrazolo-(3,4-d)-pyrimidine in combination with azaserine, 6-mercaptopurine and thioguanine. Cancer Res. 20, 1618 (1960).
Henderson, J. F., and I. G. Junga: Treatment of ascites tumors with4-aminopyrazolo-(3,4-d)-pyrimidine alone and in combination with azaserine, thioguanine and 6-mercaptopurine. Cancer Res. 21,C S 7(1961).
Herr, R. R.: Structures of streptovitacins. Amer. J. chem. Soc. 81, 2595 (1959).
Herr, R. R., M. E. Bergy, T. E. Eble and H. K. Jahnke: Porfiromycin, a new antibiotic. II. Isolation and characterization. Conference on Antimicrobial Agents, October 26–28, 1960, Washington.
Hertz, R., T. M. Bergenstal, M. B. Lipsett, E. B. Price and T. F. Hilbisch: Chemotherapy of choriocarcinoma and related trophoblastic tumors in women. J. Amer. med. Ass. 168, 845 (1958).
Hibino, S.: Chemotherapy of leukemia and allied diseases, with special reference to mitomycin C and other agents recently originated in Japan. 8. Internat. Krebscongress, Moskau 1962, S. 339.
Hirata, Y., and K. Nakaniski: Antibiotic substance from Actinomyces flavus. J. Antibiot. (Tokyo) 2, 189 (1948).
Hirata, Y., and K. Nakaniski: Actinomycin J2, a by-product from a strain of actinomyces. Bull. Soc. chem. Japan 22, 121 (1949).
Hogeboom, G. H., and W. C. Schneider: Cytochemical studies. VI. The synthesis of diphosphopyridine nucleotide by liver cell nuclei. J. biol. Chem. 197, 611 (1952).
Holzer, E., U. H. Kröger: Zum carcinostatischen Wirkungsmechanismus von Äthylen - imin-Verbindungen. Biochem. Z. 330, 579 (1958).
Holzer, E., P. Glogner U. G. Sedlmayer: Zum Mechanismus der Glykolysehemmung durch carcinostatisch wirkende Äthylenimin-Verbindungen. Biochem. Z. 330, 59 (1958).
Holzer, E., u. H. J. Boltze: Über die Wirkung von Nicotinsäureamid auf die Glykolysehemmung von Ascitestumorzellen durch Äthylenimin-Verbindungen. Z. Krebsforsch. 64, 113 (1961).
Homburger, F., A. B. Russfield, J. R. Baker and A. Tregier: Experimental chemotherapv in chemically induced mouse tumors and their transplants. Cancer Res. 22, 368 (1962).
Hooper, I. R., L. C. Chenney, M. J. Cron, O. B. Fardig, D. A. Johnson, D. L. Johnson, F. M. Palermiti, H. Schmitz and W. B. Wheatley: Studies on sarcomycin. Antibiot. and Chemother. 5, 585 (1955).
Hsü, B., M. C. Liu, K. H. LU, W. Y. LI, J. T. Ch’eng, T. Y. Wang, C. H. Chou, S. N. Koo and L. C. Shen: Actinomycin K, and antibiotic against tumor. Chin. med. J. 78, 413 (1959).
Hübener, H. J.: Die physiologische Funktion der Nebennierenrinden-Hormone als Enzym-Induktoren. Dtsch. med. Wschr. 87, 438 (1962).
Huennekens, F. M., M. J. Osborn and H. R. Whiteley: Folic acid coenzymes. Science 128, 120 (1958).
Huggins, C.: Hormonabhängige Geschwülste—klinisch und experimentell. Klin. Wschr. 1958, 1102; Ann. Surg. 115, 1191 (1942).
Huggins, C., and C. V. Hodges: Studies on prostatic cancer. I. The effect of castration of estrogen and of androgen injection on serum phosphatases in metastatic carcinoma of the prostate. Cancer Res. 1, 293 (1941).
Huguenin, R., R. Truhaut et J. S. Bourdin: Experimentation de l’actinomycine. Presse méd. 62, 740 (1954).
Hultin, T., and A. Von Der Decken: The transfer of soluble polynucleotides to the ribonucleic acid of rat liver microsomes. Exp. Cell Res. 16, 444 (1959).
Hurlbert, R. B., and H. O. Kämmen: Formation of cytidine nucleotides from uridine nucleotides by soluble mammalian enzymes: Requirements for glutamine and guanine nucleotides. J. biol. Chem. 235, 443 (1960).
Hurley, J. D., E. H. Ellison, J. Riesch and W. Schulte: Chemotherapy of solid carcinoma. J. Amer. med. Ass. 174, 1696 (1960).
Hutchings, B. L.: Ciba Foundation Symp. 1957, Chemistry and Biology of Purines. S. 177.
Iijima, T., and A. Hagiwara: Mutagenic action of mitomycin C on escherichia coli. Nature (Lond.) 185, 395 (1960).
Ikawa, M., J. B. Koepfli, S. G. Mudd and C. Niermann: An agent from e. coli causing hemorrhage and regression of an experimental mouse tumor. I. Isolation and properties. J. Nat. Cancer Inst. 13, 157 (1952).
Ishihara, T.: Clinical experience with carzinophilin. Rinsho Fujinka Sanka 12, 58 (1958).
Ishu, Y.: Anti-cancerous effect of carzinophilin. Asian med. J. 1, 34 (1958).
Ishiyama, S., H. Takahashi, I. Ishiyama, S. Shirado, M. Ida, S. Sumita, S. Izeki and Y. Shirasuga: Clinical experiences with antineoplastic antibiotic sarcomycin. Gann 45, 456 (1954).
Ishiyama, S.: Clinical observations of some malignant tumors treated with sarcomycin, a new antitumor antibiotic. J. Antibiot. Ser. A 7, 82 (1954).
Iwataru, M.: Method of preparing sarcomycin-urotropine compounds. Cancer Chemother. Abstr. 1, 4340 (1961).
Jacquez, J. A.: Active transport of o-diazoacetyl-L-serine and 6-diazo-5-oxo-L-nor- leucine in Ehrlich ascites carcinoma. Cancer Res. 17, 890 (1957).
Jacquez, J. A.: Concentrative uptake of 6-diazo-5-oxo-L-norleucine by sarcoma 180, liver and muscle in vivo. Proc. Soc. exp. Biol. Med. (N. Y.) 99, 611 (1958).
Jacquez, J. A., and D. J. Hutchison: Resistance in L 1210 ascites without change in concentrative uptake of o-diazoacetyl-L-serine or 6-diazo-5-oxo-L-norleucine. Cancer Res. 19, 397 (1959).
Jacquez, J. A., and J. H. Sherman: Enzymatic degradation of azaserine. Cancer Res. 22, 56 (1962).
Jaffe, J. J., and H. G. Mautner: A comparison of the biological properties of 6-seleno- purine, 6-selenopurine ribonucleoside, and 6-mercaptopurine in mice. Cancer Res. 20, 381 (1960).
Jagger, D. V., N. M. Kredich and A. J. Guarino: Inhibition of Ehrlich ascites tumor growth by cordycepin. Cancer Res. 21, 216 (1961).
Janbon, M.: Premier résultats de l’application de l’actinomycine C en thérapeutique. Presse Méd. 62, 741 (1954).
Johne, H. 0., u. A. Kroher: Über die Behandlung der Lymphogranulomatosis maligna (Hodgkin-Sternberg) mit Actinomycin C. Dermatologica (Basel) 109, Nr. 5 (1954).
Johnson, A. W.: Actinomycin. Spec. Publ. chem. Soc. 5, 82 (1956).
Johnson, A. W., and A. Mauger: The isolation and structure of actinomycins II and III. Biochem. J. 73, 535 (1959).
Jones jr., R., D. Mc Kenzie, M. Stevens, D. Kirkpatrick, W. Dunning and M. R. Curtis: The use of leukemia I.R.C. 741 for studies in the chemotherapy of cancer. Proc. Amer. Ass. Cancer Res. 2, 311 (1958).
Jones jr., R.: Mitomycin C. A preliminary report of studies of human pharmacology and initial therapeutic trial. Cancer Chemother. Rep. 2, 7 (1959).
Journey, L. J., and M. N. Goldstein: Electron microscope studies on HeLa cell lines sensitive and resistant to actinomycin D. Cancer Res. 21, 929 (1961).
Kamada, H., S. Wakaki, Y. Fujimoto, K. Tomioka, S. Ueyama, H. Marumo and K. Uzu: Studies on carzinophilin. I. Properties of carzinophilin A. J. Antibiot. 8, 187 (1955).
Kämmen, H. O., and R. B. Hurlbert: The formation of cytidine nucleotides and RNA cytosine from orotic acid by the Novikoff tumor in vitro. Cancer Res. 19, 654 (1954).
Amination of uridine nucleotides to cytidine nucleotides by soluble mammalian enzymes: Role of glutamine and guanosine nucleotides. Biochim. biophys. Acta (Amst.) 30, 195 (1958).
Kanamori, H., T. Shima, C. Morita and T. Hata: Studies on antitumor activity of mitomycin. J. Antibiot. (Tokyo) 10, 120 (1957).
Kaplan, L.: Studies on the action of azaserine on escherichia coli. ph. D. Thesis, Cornell Univ. 1957.
Katz, E., and W. A. Goss: Influence of amino-acids on actinomycin biosynthesis. Nature (Lond.) 182, 1668 (1958).
Katz, E., and W. A. Goss: Controlled biosynthesis of actinomycin with sarcosine. Biochem. J. 73, 458 (1959).
Katz, E.: Biogenesis of the actinomycins. Ann. N. Y. Acad. Sci. 89, 304 (1960).
Katz, E.:, and H. Weissbach: Biosynthesis of the actinomycin chromophore; enzymatic conversion of 4-methyl-3-hydroxyanthranilic acid to actinocin. J. biol. Chem. 237, 882 (1962).
Kawamata, J., and H. Fujita: Separations and characterization of actinomycin that contains alloisoleucine. Med. J. Osaka Univ. 8, 743 (1958).
Kawamata, J., N. Nakabayashi, A. Kawai and T. Ushida: Experimental production of mode of action of actinomycin. Med. J. Osaka Univ. 8, 753 (1958).
Kawamata, J., N. Nakabayashi, A. Kawai and H. Fujita: Studies on the carcinogenic effect of actinomycin. Biken’s J. 2, 105 (1959).
Kawamata, J., N. Nakabayashi:Experimental production of sarcoma in mice with actinomycini. Gann 50, Suppl. 126 (1959).
Kawamata, J., and M. Imanishi: Interaction of actinomycin with deoxyribonucleic acid. Nature (Lond.) 187, 1112 (1960).
Kawamata, J. H. Fujita and A. Ikegami: Anticancer effect of actinomycinic acid. J. Antibiot. (Tokyo) Ser. A 13, 415 (1960).
Kawamata, J., and M. Imanishi: Mechanism of action of actinomycin with special reference to its interaction with deoxyribonucleic acid. Biken’s J. 4, 13 (1961).
Kersten, H., and H. M. Rauen: Degradation of deoxyribonucleic acid in escherichia coli cells treated with mitomycin C. Nature (Lond.) 190, 1195 (1961).
Kersten, H. Action of Mitomycin C in nucleic acid metabolism in tumor and bacterial cells. Biochim. biophys. Acta (Amst.) 55, 558 (1962).
Kersten, W., H. Kersten and H. M. Rauen: Action of nucleic acids on the inhibition of growth by actinomycin of neurospora crassa. Nature (Lond.) 187, 60 (1960).
Kersten, W.: Interaction of actinomycin C with constituents of nucleic acids. Biochim. biophys. Acta (Amst.) 47, 610 (1961).
Kersten, W., u. H. Kersten: Zur Wirkungsweise von Actinomycinen. II. Bildung überschüssiger Desoxyribonucleinsäure in Bacillus subtilis. Hoppe-Seylers. Z. physiol Chem. 327, 234 (1962).
Kersten, W. Biologische Wirkung, klinische Bedeutung und biochemischer WTirkungsmechanismus der Actinomycine. Habilitations-Schrift, Univ. Münster 1962.
Kirk, J. M.: The mode of action of actinomycin D. Biochim. biophys. Acta (Amst.) 42, 167 (1960).
Koga, F.: Experimental treatment of malignant tumor with antibitoics. II. Experimental treatment with a new antibiotic, carzinophilin. J. Antibiot. (Tokyo) Ser. B 7, 275 (1954).
Kondo, T.: Adverse effects of cancer chemotherapy. 8. Internat. Krebscongress, Moskau 1962, S. 321.
Korst, D. R., and O. O. Meyer: Negative effect of actinomycin D treatment in three cases of Hodgkins disease. Antibiot. Med. 1, 474 (1955).
Kröger, H., H. W. Rotthauwe, B. Ulrich U. H. Holtzer: Zum Einfluß von Carcinostatica auf den DPN-Stoffwechsel der Tumoren. I. Einbau von 14C-Ribose und 14C-Nicotinsäureamid in das DPN von Ascites-Zellen. Biochem. Z. 333,148 (1960); — II. Nachweis von DPN-Bausteinen in Ascites-Zellen. Biochem. Z. 333, 155 (1960).
Kröger, H., B. Ulrich U. H. Holzer: Wirkung carcinostatischer Verbindungen auf die Konzentration von Diphosphopyridinnucleotid in Tumoren. Arzneimittel-Forsch. 9, 598 (1959).
Lardy, H. A., D. Johnson and W. C. Murray: Antibiotics as tools for metabolic studies. I. A survey of toxic antibiotics in respiratory phosphorylation and glycolytic systems. Arch. Biochem 78, 587 (1958).
Lehr, H., and J. Berger: The isolation of a crystalline actinomycin-like antibiotic. Arch. Biochem. 23, 503 (1949).
Le Page, G. A., J. Greenlees and J. F. Fernandes: Studies of nucleic acid synthesis in ascites tumor cells. Ann. N. Y. Acad. Sci. 63, 999 (1956).
Levenberg, G., I. Melnick and J. M. Buchanan: Biosynthesis of the purines. XV. The effect of aza-L-serine and 6-diazo-5-oxo-L-norleucine on inosinic acid biosynthesis de novo. J. biol. Chem. 225, 163 (1957).
Lewis, C., H. W. Clapp, L. E. Rhuland and H. R. Reames: Porfiromycin, a new antibiotic. III. In vitro and in vivo evaluation. Conference on Antimicrobial Agents, October 26–28, 1960, Washington.
Li, M. C.: Diskussionsbemerkung, The actinomycins and their importance in the treatment of tumors in animals and man. Ann. N. Y. Acad. Sci. 89, 424 (1960).
Lindenbein, W.: Über einige interessante Aktinomycetenstämme und ihre Klassifizierung. Arch. Mikrobiol. 17, 361 (1952).
Longenecker, J. B., and E. E. Snell: Pyridoxal and metal ion catalysis of a, ß elimination reactions of serine-3-phosphate and related compounds. J. biol. Chem. 225, 409 (1957).
Lowery, O. E., and J. W. Foster: Bacterial screening of culture filtrates for synergism with selected anticancer compounds. Antibiot. and Chemotherap. 9, 232 (1959).
Lukens, L. N., and K. A. Herrington: Enzymic formation of 6-mercaptopurineribotide. Biochim. biophys. Acta (Amst.) 24, 432 (1957).
Maddock, C. L., G. J. D’angio, S. Färber and A. H. Handler: Biological studies of actinomycin D. Ann. N. Y. Acad. Sci. 89, 386 (1960).
Magee, W. E., and F. S. Eberts jr.: Studies with psicofuranine in the tumor-bearing rat. Cancer Res. 21, 611 (1961).
Magill, G. B., R. B. Golbey, D. A. Karnofsky, J. H. Burchenal, C. C. Stock, C. P. Rhoads, C. E. Crandall, S. N. Yorukoglu and A. Gellhorn: Clinical experiences with sarcomycin in neoplastic diseases. Cancer Res. 16, 960 (1956).
Magnus, D., U. K. H. Zeitler: Kombination von Röntgenstrahlen und Sanamycin bei der Behandlung von Erkrankungen des blutbildenden Systems. Strahlentherapie 98, 413 (1955).
Marino, S., in S. Shiba and T. Taguchi: Study on Mitomycin C, N. 101 (1959), Osaka Univ.
Manier, A. C., L. Eidus and L. Greenberg: A comparison of the in vitro and in vivo activity of erythromycin and spiramycin. Antibiot. and Chemother. 10, 726 (1960).
Marquart, H., U. E. Glass: Die Chromosomenzahlen in den Leberzellen von Ratten verschiedenen Alters. Chromosoma 8, 617 (1957).
Marsh, W. S., A. L. Garretson and E. M. Wesel: Streptonigrin, an antitumor agent produced by strains of streptomyces flocculus. Proc. Amer. Ass. Cancer Res. 3, 131 (1960).
Streptonigrin, an antitumor agent produced by strains of streptomyces flocculus: I. Microbiological studies. Antibiot. and Chemother. 11, 151 (1961).
Martin, R., et J. P. Munier: Premiers résultats de 12 maladies de Hodgkin traitées par l’actinomycine C. Presse méd. 62, 741 (1954).
Martin, H.: Erfahrungen bei der Behandlung der Lymphogranulomatose mit Actinomycin C. (Sanamycin) Klin. Wschr. 32, 518 (1954).
Maxwell, R. E., and V. S. Nickel: 6-diazo-5-oxo-L-norleucine, a new tumor-inhibitory substance. Microbiological studies of mode of action. Abstr. Amer. Chem. Soc. Meeting p. 15 M (1956).
Mayevsky, M. N., R. N. Kuchkaryov, YE. A. Romanenko, A. P. Urazova, Y. N. Molkov, YE. A. Timofeyevskaya, A. S. Bondareva, V. G. Mazayeva, V. A. Talyzina and S. I. Vyazova: Antitumor activity of olivomycin (16749) and antibiotic 2703. 8. Internat. Krebscongress, Moskau 1962, S. 363.
Merker, P. C., and G. W. Woolley: A study of human epidermoid carcinoma (H. Ep. 3). Growing in conditioned swiss mice. I. Applicability to chemotherapy studies. Cancer Res. 19, 664 (1959).
Merker, P. C., F. K. Pearce, J. S. Sarino and G. W. Woolley: The effect of streptonigrin and other antibiotics on human epidermoid carcinoma H. Ep. 3 growing in conditioned swiss mice. Antibiot. and Chemother. 11, 184 (1961).
Merz, T.: Effect of mitomycin C on lateral root-tip chromosomes of vicia faba. Science 133, 329 (1961).
Miller, E., and R. D. Sullivan: Clinical effects of the continuous intravenous infusion of cancer chemotherapeutic compounds. 8. Internat. Krebscongress, Moskau 1962, S. 338.
Miller, T. R., and G. Mc Lemore: zitiert in B. Sokoloff: Progress in cancer chemotherapy: The oncolytic antibiotics. Progr. exper. Tumor Res. 1, 360 (1960).
Milton, D., N. Goldstein, J. I. Slotnick, M. H. Hillman and C. Gallagher: Cytochemical and biochemical studies on HeLa cells sensitive and resistant to actinomycin D. Proc. Amer. Ass. Cancer Res. 3, 23 (1959).
Molkov, Ye. N.: Use of tumour-inhibiting antibiotics for prevention and treatment of relapses and metastases in experimental cancer. 8. Internat. Krebscongress Moskau, 1962, S. 367.
Moore, J. A., J. R. Dice, E. D. Nicolaides, R. D. Westland and E. L. Wittle: Azaserine, synthetic studies. J. Amer. chem. Soc. 76, 2884 (1954).
Moore, E. C., and G. A. Le Page: In vivo sensitivity of normal and neoplastic mouse tissues to azaserine. Cancer Res. 17, 804 (1957).
Moore, G. E., T. Kondo and J. Badillo: Clinical trial of actinomycin D. Proc. Amer. Ass. Cancer Res. 2, 328 (1958).
Moore, G. E., J. A. Di Paolo and I. Kondo: The chemotherapeutic effects and complications of actinomycin D in patients with advanced cancer. Cancer 11, 1204 (1958).
Moore, E. C., and R. B. Hurlbert: Biosynthesis of RNA cytosine and RNA purines: differential inhibition by diazo-oxo-norleucine. Cancer Res. 21, 257 (1961).
Morris, N. R., and G. A. Fischer: Studies concerning inhibition of the synthesis of desoxycytidine by phosphorylated derivatives of thymidine. Biochim. biophys. Acta (Amst.) 42, 183 (1960).
Mueller, G. C., J. Gorski and Y. Aizawa: The role of protein synthesis in early estrogen action. Proc. nat. Acad. Sei. (Wash.) 47, 164 (1961).
Mühlbock, O.: Der Einfluß von Hormonen auf den Tumor. Klin. Med. 3, 355 (1960). ( Berliner Symp. Carcinogenese Dez. 1959 ).
Murphy, M. L., and D. A. Karnofsky: Effect of azaserine and other growth-inhibiting agents on fetal development of the rat. Cancer 9, 955 (1956).
Nakata, A., M. Sekiguchi and J. Kawamata: Inhibition of multiplication of bacteriophage by actinomycin. Nature (Lond.) 189, 246 (1961).
Narrod, S. A., T. A. Langan jr., N. O. Kaplan and A. Goldin: Effect of azaserine (o-diazoacetyl-L-serine) on the pyridine nucleotide levels of mouse liver. Nature (Lond.) 183, 1647 (1959).
Narrod, S. A. V. Bona Vita, E. R. Ehrenfeld and N. O. Kaplan: Effect of azaserine on the biosynthesis of diphosphopyridine nucleotide in mouse. J. biol. Chem. 236, 931 (1961).
Nathans, D., and F. Lipmann: Amino acid transfer from aminoacyl-ribonucleic acids to protein on ribosomes of escherichia coli. Proc. Nat. Acad. Sci. (Wash.) 47, 497 (1961).
Nemeth, A. M., and G. De La Haba: The effect of puromycin on the development and adaptive formation of tryptophan pyrrolase. J. biol. Chem. 237, 1190 (1962).
Nichol, C. A., and A. D. Welch: On the mechanism of action of aminopterin. Proc. Soc. exp. Biol. (N. Y.) 74, 403 (1950).
Nitsch, W., U. K. Thein: Beitrag zur Behandlung der Lymphogranulomatose mit Sanamycin. Ther. d. Gegenw. 94, 49 (1955).
Nitta, K.: Studies on the effects of actinomycetes products on the culture of human carcinoma cells (strain He La). II. The effect of known antitumor antibiotics on He La cells. Jap. J. med. Sci. Biol. 10, 287 (1957).
Oata, K., A. Nishibori and I. Hayashi: Experimental study on the oncostatic activity of Actinomycin J. I. Histological findings of therapeutic effects on Ehrlich’s mouse ascites carcinoma in the ddN strain mice. II. Effects on the Yoshida ascites sarcoma in stock rats. J. Antibiot. (Tokyo) 10, 46, 56 (1957).
Oettel, H., U. G. Wilhelm: Vergleichende Prüfung von 14 cytostatisch wirksamen Produkten an 7 Tiertumoren. Naunyn-Schmiedeberg’s Arch. exp. Path. Pharmak. 230, 559 (1957).
Ohara, T.: The study on the chemotherapy of gastric cancer. Preliminary report. Proc. Jap. Cancer Ass. 19th Meeting 1960, S. 79.
Old, L. J., D. A. Clarke, B. Benacerraf and M. Goldsmith: The reticuloendothelial system and the neoplastic process. Ann. N. Y. Acad. Sci. 88, 264 (1960).
Oleson, J. J., L. A. Calderella, K. J. Myos, A. R. Reith, R. S. Thie and I. Toplin: Theeffects of streptonigrin on experimental tumors. Antibiot. and Chemother. 11, 158 (1961).
Olmer, J.: Essais de traitement de certains hemopathies malignes par Factinomycme C. Presse med. 62, 742 (1954).
Osborn, M. J., M. freeman and F. M. Huennekens: Inhibition of dihydrofolic reductase by aminopterin and amethopterin. Proc. Soc. exp. Biol. (N. Y.) 97, 429 (1958).
Osten, W., u. Zademack: Klinische Erfahrungen mit Sanamycin bei Lymphogranulo-matose. Medizinische 18, 687 (1955).
Otsuji, N., M. Sekiguchi, T. Iijiama and Y. Takagi: Induction of phage formation in the lysogenic escherichia coli K-12 by mitomycin C. Nature (Lond.) 184, 1079 (1959).
Paul, R., et S. Tchelitcheff: Structure de la spiramycine. III. Étude des produits de dégradation caracterisation du mycaminose. Bull. Soc. chim. Fr. 734, 1059 (1957).
Pellerat, J., et M. A. Maillard: Fixation tissulaire de la spiramycine chez le cobaye: comparison avec d’autres antibiotiques. C. R. Acad. Sci. (Paris) 247, 894 (1958).
Peters, J. M., and D. M. Greenberg: Studies on folic acid reduction. Biochim. biophys. Acta (Amst.) 32, 273 (1959).
Philips, F. S., H. S. Schwartz and S. S. Sternberg: Pharmacology of Mitomycin C. I. Toxicity and pathologic effects. Cancer Res. 20, 1354 (1960).
Philips, F. S., H. S. Schwartz and S. S. Sternberg and CH. T. C. Tan: The toxicity of actinomycin D. Ann. N. Y. Acad. Sci. 89, 348 (1960).
Pine, E. K.: Concentrative uptake of azaserine by neoplastic plasma cells and lympho¬cytes. J. Nat. Cancer Inst. 21, 973 (1958).
Pinkel, D.: Actinomycin D in childhood cancer. Pediatrics 23, 342 (1959).
Pinnert-Sindico, S., L. Ninet, J. Preud’homme and S. Cosar: A new antibiotic — spiramycin in: H. Welch and F. Marti-ibanez: Antibiot. Ann. 1954–1955, N. Y. Medical Encyclopedia, Inc. 1955, S. 724.
Porter, J. N., R. I. Hewitt, C. W. Hesseltine, G. Krttpka, J. A. Lowery, W. S. Wallace, N. Bohonos and J. H. Williams: Achromycin: A new antibiotic having trypanocidal properties. Antibiot. and Chemother. 2, 409 (1959).
Potter, V. R.: Sequential blocking of metabolic pathways in vivo. Proc. Soc. exper. Biol. (N. Y.) 76, 41 (1951).
Potter, M., and L. W. LAW: Studies of a plasma-cell neoplasma of the mouse. I. Characterization of neoplasma 70429 including its sensitivity to various antimetabolites with the rapid development of resistance to azaserine, DON, and N-methylformamide. J. Nat. Cancer Inst. 18, 413 (1957).
Potter, V. R.: The biochemical approach to the cancer Problem. Fed. Proc. 17, 691 (1958)
Preiss, J., and P. Handler: Biosynthesis of diphosphopyridine nucleotide. II. Enzymatic aspects. J. biol. Chem. 233, 493 (1958).
Pridham, T. E., C. W. Hesseltine and R. G. Benedict: A guide for the classification of streptomycetes according to selected groups. — Plasment of strains in morphological section. Appl. Microbiol. 6, 52 (1958).
Pugh, L. H., and M. Solotorovsky: Comparative effects of actinomycins II, III, and IV on several ascitic tumors in mice. Ann. N. Y. Acad. Sci. 89, 373 (1960).
Pugh, L. H., E. Katz and S. A. Waksman: Antibiotic and cytostatic properties of the actinomycines. J. Bact. 72, 660 (1956).
Rampan, J. I., and A. B. Syrkin: Studies on pharmacology of the new antitumor antibiotics (actinoxantin, aurantin, 2703, fumagillin). 8. Internat. Krebscongress, Moskau, 1962, S. 553.
Rao, K. V., S. C. Brooks jr., M. Kugelman and A. A. Romano: Diazomycins A, B, and C, three antitumor substances. I. Isolation and characterization. In: H. Welch and F. Marti-Ibanez: Antibiot. Ann. 1959–1960, N. Y., Medical Encyclopedia. Inc. 1960, S. 943.
Rao, K. V. and W. P. Cullen: Streptonigrin, an antitumor substance. I. Isolation and characterization. In H. Welch and F. Marti-Ibanez: Antibiotics Ann. 1959–1960. N. Y. Medical Encyclopedia 1960, S. 950.
Rauen, H. M., H. Kersten U. W. Kersten: Zur Wirkungsweise von Actinomycinen. Hoppe-Seylers Z. physiol. Chem. 321, 139 (1960).
Ravina, A., M. Pestel et R. Thielen: Klinische Verwendung der cytostatischen und antitumoralen Eigenschaften des Actinomycin C (Sanamycin). Presse méd. 62, 1159 (1954); Quelques exemples de malades traités par l’actinomycine C. Bull. Soc. méd. Hôp. Paris 32, 33, 34, 1206 (1954).
Ravina, A., M. Pestel: Die Actinomycine. 30. Cong, franç. méd. Algier 1955. Presse méd. 62, 743 (1954).
Ravina, A., et PH. Eloy: État actuel de la chimiothérapie anticancéreuse. I. — Les antibiotiques et les substances provencent des végétaux supérieurs. Presse méd. 68, 1359 (1960).
Ravina, A., and M. Pestel: The clinical applications and methods of administration of actinomycin in the treatment of different tumors. Ann. N. Y. Acad. Sci. 89, 463 (1960).
Reich, E., A. J. Shatkin and E. L. Tatum: Bacteriocidal action of mitomycin C. Biochim. biophys. Acta (Amst.) 53, 132 (1981).
Reich, E., R. M. Franklin, A. J. Shatkin and E. L. Tatum: Effect of actinomycin D on cellular nucleic acid synthesis and virus production. Science 134, 556 (1961).
Reichard, P., O. Sköld and G. Klein: Possible enzymic mechanism for the development of resistance against fluorouracil in ascites tumors. Nature (Lond.) 183, 939 (1959).
Reilly, H. C., A. Schatz and S. A. Waksman: Antifungal properties of antibiotic substances. J. Bact. 49, 585 (1945).
Reilly, H. C.: Inactivation of azaserine by a liver enzyme. Fed. Proc. 13, 279 (1954).
Reilly, H. C.: The effect of amino acids upon the antimicrobial activity of azaserine. Proc. Amer. Ass. Cancer Res. 1, 40 (1954).
Reilly, H. C., J. G. Cappuccino and D. M. Harrison: Studies on mitomycin C, a tumor-inhibiting antibiotic. Proc. Amer. Ass. Cancer Res. 2, 338 (1958).
Reilly, H. C., and K. SUGIURA: An antitumor spectrum of streptonigrin. Antibiot. and Chemother. 11, 174 (1961).
Riegel, R., U. K. Krückemeyer: Die Behandlung des großfollikulären Lymphoblastoms (M. BriU-Symmers) mit Sanamycin “Bayer”. Ärztl. Wschr. 12, 160 ((957).
Ritter, L.: Die Lymphogranulomatose-Behandlung aus chirurgischer Blickrichtung. Münch, med. Wschr. 96, 1484 (1954).
Robinson, H. J.: Studies on the toxicity of actinomycin. J. Pharmacol, exp. Ther. 74, 25 (1942).
Roitt, I. M. I.: The inhibition of carbohydrate metabolism in ascites-tumour-cells by ethyleneimines. Biochem. J. 63, 300 (1956).
Ross, G. T., L. L. Stolbach and R. Hertz: Actinomycin D in the treatment of methotrexat-resistant trophoblastic disease in women. Cancer Res. 22, 1015 (1962).
Rounds, D. E., Y. H. Nakanishi and C. M. Pomerat: Possible mechanisms to explain the action of actinomycin on nonmalignant and malignant cells. Antibiot. and Chemother. 10, 597 (1960).
Sakai,K.,and T. Teranaka: On antitumor activity of mitomycin against experimental animal tumors. Chemotherap. 5, 222 (1957).
Sakai,K., K. Yoshimura, K. Hayashi, F. Marui, T. Kimura, A. Sawada and K. Hashima: Studies on tumor inhibiting activity of mitomycin. Chemotherap. 5, 322 (1957).
Salser, J. S., and N. E. Balis: Studies on the mechanism of action of 6-mercaptopurine (6 MP) in cell-free preparations. Fed. Proc. 18, 315 (1959).
Sartorelli, A. C., and G. A. Le Page: Biochemical basis for resistance of a TA 3 Ascites carcinoma to azaserine. Proc. Amer. Ass. Cancer Res. 2, 245 (1957).
Sartorelli, A. C. The development and biochemical characterization of resistance to azaserine in a TA 3 ascites carcinoma. Cancer Res. 18, 457 (1958).
Sartorelli, A. C. Inhibition of ascites cell growth by combinations of 6-thioguanine and azaserine. Cancer Res. 18, 938 (1958).
Sartorelli, A. C., and B. A. Booth: Antineoplastic activity of combinations of 6-chloropurine and azaserine. Cancer Res. 20, 198 (1960).
Sartorelli, A. C., P. F. Kruse jr., B. A. Booth and E. J. Schoolar jr.: Combination chemotherapy: treatment of ascitic neoplasms by purine, amino acid, and vitamin analogs. Cancer Res. 20, CS 495 (1960).
Sartorelli, A. C., E. J. Schoolar jr. and P. F. Kruse jr.: Chemotherapy of sarcoma 180 by combinations of DL-glyceraldehyde with 6-thioguanine or with azaserine and 6-chloropurine. Proc. Soc. exp. Biol. (N. Y.) 104, 266 (1960).
Sasakawa, S., T. Nurishima, E. Sawada, K. Norita, M. Sasaki and T. Fujiia: Clinical experience of carcinophilin in the gastroscirrhus. Shinyaku to Rinsko 7, 76 (1958).
Sayanagi, T.: Med. J. Osaka Univ. 11, 3947 (1959).
Schabel, jr. F. M., H. E. Skipper, J. G. Fortner, J. R. Thomson, W. R. Laster jr., J. H. Moore, C. A. Kelley and D. R. Farnell: Experimental evaluation of potential anticancer agents. II. Studies on the growth characteristics, metastases, and drug response of hamster neoplasms of diverse “Sites of origin”. Cancer Res. 21, 235 (1961). Cancer Chemother. Screening Data X.
Schmidt, C. G.: Über die Biologische Oxydation und Glykolyse in Tumoren. Klin. Wschr. 1955, 409.
Schmidt, C. G.: Über die Hemmung der Glykolyse von Tumorzellen durch Carcinophilin. Klin. Wschr. 1960, 334.
Schmidt, C. G.: Über den Einfluß von Carcinophilin und Mitomycin C auf die Atmung und Glykolyse von Tumorzellen. Oncologia (Basel) 18, 426 (1960).
Schmidt, C. G.: Energiestoffwechsel von Tumorzellen im Hinblick auf die Einwirkung von Cytostatica. Symposium über Krebsprobleme. Düsseldorf 1960, S. 108. Berlin-Göttingen- Heidelberg: Springer 1961.
Schmidt, C. G.: Über Beziehungen zwischen DPN(Diphosphopyridinnucleotid) -Konzentration und Glykolysehemmung von Tumorzellen durch Carcinophilin. Z. Krebsforsch. 64, 156 (1961).
Schmidt, C. G.: Beeinflussung des Kohlenhydratstoffwechsels von Tumorzellen durch Carcinophilin. Z. Krebsforsch. 64, 328 (1961).
Schmidt, C. G.: Einfluß von Antibiotica auf den Tumorstoffwechsel. Oncologia (Basel) 15, 144 (1962).
Schmidt, C. G.: The effect of carcinostatic compounds on carbohydrate metabolism of tumor cells. Extr. Acta Union Internat. Contre Le Cancer 18, 240 (1962).
Schmidt, H., U. H. Waetin: Über die Behandlung eines metastasierenden Hyper-nephroma mit Sanamycin. Med. Klin. 49, 1369 (1954).
Schmidt, C. G., H. Loosen U. W. Heinen: Sanamycin (Actinomycin C) in der Behandlung bösartiger Geschwülste und der Lymphogranulomatose. Dtsch. med. Wschr. 80, 140 (1955).
Schmidt-Kastner, G.: Über neue biosynthetische Actinomycine. Med. u. Chem. 5, 463 (1956).
Schmidt, C. G., Actinomycin E und F, zwei neue biosynthetische Actinomycingemische. Natur-wissenschaften 43, 131 (1956).
Schmidt, C. G., The production of actinomycins by controlled biosyntheses: The F actinomycins. Ann. N. Y. Acad. Sci. 89, 299 (1960).
Schmidt, C. G., u. A. Bohne: DBP 944, 395.
Schmitz, H., W. T. Bradner, A. Gotjrevitch, B. Heinemann, K. E. Price, J. Lein and I. R. Hooper: Actinogan: A new antitumor agent obtained from streptomyces. I. Chemical and biological properties. Cancer Res. 22, 163 (1962).
Schroeder, W., and H. A. Hoeksema: A new antibiotic, 6-amino-9-D-psicofuranine. J. Amer. chem. Soc. 81, 1767 (1959).
Schulte, G.: Erfahrungen mit neuen cytostatischen Mitteln bei Hämoblastosen und Carcinomen und die Abgrenzung ihrer Wirkungen gegen Röntgentherapie. Z. Krebsforsch. 58, 500 1(952).
Schulte, G.: Erfahrungen mit neuen cytostatischen Mitteln bei Hämoblastosen und Carcinomen und die Abgrenzung ihrer Wirkung gegen Röntgentherapie; Weitere Erfahrungen mit Sanamycin bei der Behandlung der Lymphogranulomatose. Kongreß Dtsch. Röntgen- Ges. Wiesbaden 1952, Stuttgart, 1953.
Schulte, G.: u. H. Lings: Erfahrungen mit neuen zytostatischen Mitteln bei Leukosen und Lymphogranulomatosen und die Abgrenzung ihrer Wirkungen gegen Röntgentherapie. Strahlentherapie 90, 301 (1953).
Schulte, G.: Weitere Erfahrungen mit Sanamycin bei der Behandlung der Lymphogranulomatose. Strahlentherapie 94, 491 (1954).
Schulten, H., U. W. Pribilla: Tumorbehandlung mit cytostatischen Substanzen. Med. Klin. 50, 1631 (1955).
Schultze, H.: Kasuistischer und therapeutischer Beitrag zum Plasmozytom-Problem. Sammlung seltener klinischer Fälle. Heft 15, 97 Leipzig: Thieme 1958.
Schwenkenbecher, H., U. H. Hillger: Die kombinierte Behandlung der Lympho-granulomatose mit Röntgenstrahlen und Sanamycin. Med. Klin. 51, 263 (1956).
Scriba, P., S. Schneider U. H. Holzer: Zur Wirkung von 2,5-Dimethoxy-äthoxy-3,6- bis-äthyleniminobenzochinon-1,4 (Bayer A 139) auf die Glykolyse von Ascites-Tumor- zellen. Z. Krebsforsch. 63, 547 (1960).
Sekiguchi, M., and G. Takagi: Synthesis of deoxyribonucleic acid by phage-infected escherichia coli in the presence of mitomycin C. Nature (Lond.) 183, 1134 (1959); Virology 10, 160 (1960).
Shanbrom. E.: Advances in cancer chemotherapy. J. chron. Dis. 13, 69 (1961).
Shiba, S., A. Terawaki, T. Taguchi and Y. Kawamata: Selective inhibition of formation of deoxyribonucleic acid in escherichia coli by mitomycin C. Nature (Lond.) 183, 1056 (1959).
Shima, T., H. Kanamori, T. Hoshi, C. Morita and T. Hata: Study on treatment with mitomycin against experimental malignancy. Chemotherap. 4, 304 (1956).
Shimada, N.: Clinical experiences with carzinophilin. Gann 47, 465 (1956).
Shimada, N., Y. Ishii, Y. Sato, T. Hatori, T. Fukui, K. Ktjbouchi, M. Sudo, T. Noguchi, K. Sukigara and T. Takeishi: The summary of clinical effects of carzinophilin. Keio J. Med. 5, 1 (1956).
K. Kubota, K. Sukie, T. Noguchi and T. Takeishi: Experimental and clinical studies on mitomycins A and X. Chemotherap. 4, 305 (1956).
K. Kubota: Clinical experiments with carzinophilin. Nihon Ishikai Zasshi 33, 264 (1958).
Shiraha, Y., K. Sakai and T. Teranaka: Clinical trials of mitomycin, a new antitumor antibiotic. Antibiot. Ann. 1958–1959 N. Y. Medical Encyclopedia Inc. S. 533 (1959).
Shiraha, Y.: Further observation on the clinical effectiveness of mitomycin C, an antitumor antibiotic. Antibiot. Ann. 1959—1960, 970.
Shorin, V. A., O. K. Rossolimo, L. Ye. Goldberg, M. S. Stantslavskaya, N. A. Blumberg, u. M. P. Vertogradova: New methods of cancer treatment (antibiotics, chemotherapy). Experimental study of the antitumor antibiotic olivomycin. 8. internat. Krebscongress, Moskau 1962, S. 364.
Sivak, A., and E. Katz: Bacteriol. Proc. 58/Ä General Meeting Soc. Am. Bacteriol. St. Louis 1959, S. 124. A pathway for tryptophan oxidation in Streptomyces antibioticus.
Sivak, A., F. Nobili and E. Katz: Biogenesis of the chromopeptide actinomycin. Bact. Proc. 1960, 149.
Skipper, H. E., J. R. Thomson and M. Bell: Attempts at dual blocking of biochemical events in cancer chemotherapy. Cancer Res. 14, 503 (1954).
Skipper, H. E., L. L. Bennett jr. and F. M. Schabel jr.: The mechanism of action of azaserine. Fed. Proc. 13, 298 (1954).
Skipper, H. E.: Annual Prog. Rep. on Cancer Chemoth. and mechanism of action of anticancer drugs. Southern Res. Inst. Birmingham, Alabama (1955).
Slechta, L.: Studies on the mode of action of psicofuranine. Biochem. Pharmacol. 5, 96 (1960).
Slotnick, I. J.: Studies on the mechanism of action of actinomycin D. II. Interference with ammonia assimilation and adaptive enzyme formation. Antibiot. and Chemother. 8, 476 (1958).
Smith, C. G.: Tissue culture. Bioassay methods for Streptovitacin A. Proc. Soc. exp. Biol. (N. Y.) 100, 757 (1959).
Smith, C. G., W. L. Lummis and J. E. Grady: An improved tissue culture assay. II. Cytotoxicity studies with antibiotics, chemicals, and solvents. Cancer Res. 19, 847 (1959).
Smith, C. G.: Studies on the mode of action of streptovitacin A. Cancer Res. 20, 1394 (1960).
Smith, C. G.: An improved tissue culture assay. I. Methodology and cytotoxicity of anti-tumor agents. Cancer Res. 19, 843 (1959).
Sokoloff, B., K. Nakabayashi, K. Enomoto, T. R. Miller, A. Bicknell, L. Bird, W. Trauner, Y. Niswonger and G. Renninger: Experimental studies on mitomycin C. I. Growth 23, 109 (1959).
Sokoloff, B.: Progress in cancer chemotherapy: The oncolytic antibiotics. Progr. exp. Tumor Res. 1, 360 (1960).
Sokoloff, B., and B. Mc Connell: Host defence and chemotherapy in experimental cancer. 8. Internat. Krebscongress, Moskau 1962, S. 323.
Sokolski, W. T., N. J. Eilers and G. M. Savage: Antibiotics Ann. S. 551. Med. Encyclopedia N. Y. 1959.
Sternberg, ST. S., F. S. Philips and A. P. Cronin: The sites of action of mitomycin C: Comparison with other chemotherapeutic agents. Proc. Amer. Ass. Cancer Res. 3, 66 (1959).
Stock, C. C., H. C. Reilly, S. M. Buckley, D. A. Clarke and C. P. Rhoads: Azaserine, a new tumor inhibitory substance. Nature (Lond.) 173, 71 (1954).
Stock, C. C., H. C. Reilly, S. M. Buckley, D. A. Clarke and C. P. Rhoads: Azaserine, a tumor inhibitory antibiotic. Acta Un. int. Cancr. 11, 186 (1955).
Stock, C. C., K. Sugiura and C. P. Rhoads: The influence of antibiotic preparations on the viability and growth of sarcoma, melanoma and carcinoma in mice. Acta Un. int. Cancr. 6, 550 (1948).
Stock, C. C., A. Clarke, F. S. Philips and R. K. Barclay: Sarcoma 180 screening data. Cancer Res. 20, CS 1 (1960).
Sugawara, R., and T. Hata: Mitomycin, a new antibiotic from streptomyces. 2. Description of the strain. J. Antibiot. (Tokyo) Ser. A. 9, 147 (1956).
Sugiura, K., and C. C. Stock: Effect of o-diacetyl-L-serine (Azaserine) on growth of various mouse and rat tumors. Proc. Soc. exp. Biol. (N. Y.) 88, 127 (1955).
Sugiura, K., and H. J. Creech: Merits of ascites tumors for chemotherapeutic screening. Ann. N. Y. Acad. Sci. 63, 962 (1956).
Sugiura, K., C. C. Stock, H. C. Reilly and M. M. Schmid: Studies in a tumor spectrum. VII. The effect of antibiotics on the growth of a variety of mouse, rat, and hamster tumors. Cancer Res. 18, 66 (1958).
Sugiura, K., C. C. Stock: The effect of mitomycin on a spectrum of tumors. Proc. Amer. Cancer Res. 2, 350 (1958).
Sugiura, K., C. C. Stock:Effect of compounds on the friend mouse virus leukemia. Proc. 7. Internat. Cancer Congress (London) 187 (1958).
Sugiura, K.: Studies in a tumor spectrum. VIII. The effect of mitomycin C on the growth of a variety of mouse, rat, and hamster tumors. Cancer Res. 19, 438 (1959).
Sugiura, K.: The effect of actinomycin Dona spectrum of tumors. Ann. N. Y. Acad. Sci. 89, 368 (1960).
Sugiura, K.: Experimental chemotherapy of cancer. — A report of progress. Progr. exp. Tumor Res. 2, 332 (1961).
Sukie, K., T. Takeishi and T. Noguchi: Clinical application of mitomycin C. Chemothe- rap. 5, 223 (1957).
Tachibana, J.: Histopathological studies on autopsied cases of stomach cancer treated with anticancerous drugs. Tohoku J. exp. Med. 76, 279 (1961).
Taguchi, T., S. Shiba, I. Ito, M. Matsui, T. Fujii, M. Yamamoto, S. Sawada, Y. Omukai, E. Yamamoto, K. Horino, A. Terawaki, M. Neda, T. Nenishi and H. Kontani: Clinical experience with mitomycin C. Gann (suppl.) 49, 16 (1959).
Takeishi, T.: Effect of carzinophilin on the bone marrow. Chemotherap. 4, 252 (1956).
Tal, M., and D. Elson: The reversible release of protein, ribonucleic acid and deoxy- ribonuclease from ribosomes. Biochim. biophys. Acta (Amst.) 53, 227 (1961).
Talley, R. W., Y. L. Beckett and J. E. Kelley: Streptovitacin A: Clinical trial. Proc. Amer. Ass. Cancer Res. 3, 155 (1960).
Tan, C. T. C., H. W. Dargeon and J. H. Burchenal: The effect of actinomycin D on cancer in childhood. Pediatrics 24, 544 (1959).
Tan, C. T. C., R. B. Golbey, C. L. Yap, N. Wollner, C. A. Hackethal, L. M. Murphy, H. W. Dargeon and J. H. Burchenal: Clinical experience with actinomycins D, KS 2, and F 1 (KS 4). Ann. N. Y. Acad. Sci. 89, 426 (1960).
Tapie, J.: Résultats de l’emploi de l’actinomycine C en thérapeutique. Presse méd. 63, 1684 (1955).
Tarnowsky, G. S., and C. C. Stock: Effects of combination of azaserine and of 6-diazo- 5-oxo-L-norleucine with purine analogs and other antimetabolites on the growth of two mouse mammary carcinomas. Cancer Res. 17, 1033 (1957).
Teller, M. N., P. C. Merker, J. E. Palm and G. W. Wolley: Transplantable human tumors in experimental chemotherapy: Effects of actinomycins on H. S. 1 and H Ep 3 in the rat. J. Nat. Cancer Inst. 28, 353 (1962).
Teranaka, T.: Studies on antitumor activities of mitomycin X. I. An experimental evaluation of antitumor activities of mitomycin X upon animal cancers. J. Osaka med. Center 7, 24 (1958).
Teranaka, T: Evaluation of antitumor activity of mitomycin. J. Antibiot. (Tokyo) Ser. A 10, 126 (1958).
Teller, H.: Zur Kasuistik der Retikulosarkomatosen. Derm. Wschr. 139, Heft 7. (1959)
Themann, H., U. C. G. Schmidt: Elektronenmikroskopische Untersuchungen über den Einfluß von Äthyleniminchinonen (E 39) und von Carzinophilin auf Ascitestumorzellen. Beitr. path. Anat. 123, 62 (1960).
Beeinflussung der sublichtmikroskopischen Struktur von Tumorzellen durch Cytostatika. Symposium über Krebsprobleme, S. 95, Düsseldorf 1960. Berlin-Göttingen- Heidelberg: Springer-Verlag 1961.
Thorne, C. B., C. G. Gomez and R. D. Housewright: Transamination of D-amino acids by bacillus subtilis. J. Bact. 69, 357 (1955).
Thorne, C. B., and D. M. Molnar: D-amino acid transamination in bacillus anthracis. J. Bact. 70, 420 (1955).
Tomisek, A. J., H. J. Kelly and H. E. Skipper: Chromatographic studies of purine metabolism. I. The effect of azaserine on purine biosynthesis in E. coli using various C14-labeled precursors. Arch. Biochem. 64, 437 (1956).
Tomisek, A. J., M. R. Reid and H. E. Skipper: Chromatographic studies of purine metabolism. IV. Reversal of azaserine-induced inhibition by phenylalanine and tryptophan. Cancer Res. 19, 489 (1959).
Trounce, J. R., A. B. Wayte and J. M. Robson: Actinomycin C in treatment of advanced Hodgkin’s disease. Brit. med. J. 1955 II, 1418.
Trussel, P. C., and E. M. Richardson: Actinomycin from a new streptomyces. Canad. J. Res. 26, 27 (1948).
Tuchmann-Duplessis, H., et L. Mercier-Parot: Production de diverses malformations par administration d’actinomycine D à la ratte gestante. C. R. Soc. Biol. (Paris) 153, 386 (1959).
Tuchmann-Duplessis, H., et L. Mercier-Parot: Apropos of the teratogenic action of actinomycin. C. R. Soc. Biol. (Paris) 153, 1697 (1959).
Tuchmann-Duplessis, H., et L. Mercier-Parot: Influence of actinomycin D on gestation and fetal development in the rabbit. C. R. Soc. Biol. (Paris) 154, 914 (1960).
Tuchmann-Duplessis, H., et L. Mercier-Parot: Apropos of the teratogenic action of actinomycin D. Trials at prevention with panthothenic acid. Rev. franç. Étud. clin. biol. 5, 923 (1960).
Tulinsky, A.: The structure of mitomycin A. J. A.Er. ehem. Soc. 84, 3188 (1962).
Umezawa, H., S. Hayano, T. Takeuchi and Y. Mizuhara: Isolation of actinomycin A from a strain of streptomyces. J. Penicillin (Japan) 1, 129 (1947).
Umezawa, H., T. Takeuchi, K. Nitta, T. Yamamoto and S. Yamaoka: Sarkomycin, an anti-tumor substance produced by streptomyces. J. Antibiot. (Tokyo) Ser. A 6, 101 (1953).
Y. Okami, T. Yamamoto and S. Yamaoka: Studies on antitumor substances produced by microorganisms. III. The sarkomycin produced by a strain resembling streptomyces erythrochromogenes. J. Antibiot. (Tokyo) Ser. A 6, 147 (1953).
Y. Okami, T. Yamamoto, T. Takeuchi, T. Osato, Y. Okami, S. Yamaoka, T. Okuda, K. Nitta, K. Yagishita, R. Utahara and S. Umezawa: Sarkomycin, an anti-cancer substance produced by streptomyces. Antibiot. and Chemother. 4, 514 (1954).
Usubuchi, I.: Effect of mitomycins on experimental tumors. Chemotherap. 5, 222 (1957).
Usubuchi, I., S. Oboshi, R. Tsuchida and H. Tanabe: The effect of mitomycin C on the growth of a variety of rat and mouse tumors. Gann 49, 209 (1958).
Usubuchi, I., S. Oboshi, R. Tsuchida and H. Tanabe: Chemotherap. 6, 318 (1958).
Van Rymenant, M.: Production de methemoglobine par la mitomycine C in vivo et in vitro. 8. Internat. Krebscongress, Moskau 1962, S. 553.
Vogelsang, K. H., U. A. Tobben: Ein Beitrag zur Prognose und Therapie der Lympho- granulomatose. Strahlentherapie 101, Heft 1 (1956).
Wada, Y., Y. Tanakadate, T. Masagawa, S. Hibine and K. Yamada: Side effects of anticancer chemotherapy and its treatment. Cancer Chem. Abstr. 1, 4395 (1960).
Wakaki, S., H. Marumo, K. Tomioka, G. Shimiztj, E. Kato, H. Kamada, S. Kudo and Y. Fujimoto: Isolation of new fractions of antitumor mitomycins. Antibiot. and Chemother. 8, 228 (1958).
Wakaki, S., Y. Harada, K. Uzu, G. B. Whitefield, A. N. Wilson, A. Kalowsky, E. O. Stapley, F. J. Wolf and D. E. Williams: The identity of porfiromycin and methyl mitomycin. Antibiot. and Chemother. 12, 469 (1962).
Waksman, S. A., and R. E. Curtis: The actinomyces of the soil. Soil Sci. 1, 99. (1916)
Waksman, S. A., and J. W. Foster: Associative and antagonistics effects of microorganisms. II. Antagonistic effects of microorganisms grown on artificial substrates. Soil Sci. 43, 69 (1937).
Waksman, S. A., and H. B. Woodruff: Bacteristatic and bactericidal substances produced by a soil actinomyces. Proc. Soc. exp. Biol. (N. Y.) 45, 609 (1940).
Waksman, S. A.: The soil as a source of microorganisms antagonistic to disease-producing bacteria. J. Bact. 40, 583 (1940).
Waksman, S. A.: Actinomyces antibioticus, a new soil organism antagonist to pathogenic and non-pathogenic bacteria. J. Bact. 42, 231 (1941).
Waksman, S. A., and M. Tishler: The chemical nature of actinomycin, an antimicrobial substance produced by actinomyces antibioticus. J. biol. Chem. 142, 519 (1942).
Waksman, S. A., and E. Bugie: Action of antibiotic substances upon Ceratostomella ulmi. Proc. Soc. exp. Biol. (N. Y.) 54, 79 (1943).
Waksman, S. A., W. B. Geiger and D. M. Reynolds: Strain specificity and production of antibiotic substances. VII. Production of actinomycin by different actinomycetes. Proc. Nat. Acad. Sci. (Wash.) 32, 117 (1946).
Waksman, S. A., E. Katz and L. C. Vining: Nomenclature of the actinomycins. Proc. Nat. Acad. Sci. (Wash.) 44, 602 (1958).
Waksman, S. A.,: Introduction: The actinomycins and their importance in the treatment of tumors in animals and man. Ann. N. Y. Acad. Sci. 89, 285 (1960).
Wallach, D. P., and R. C. Thomas: Psicofuranine VIII. Some pharmacological ob¬servations. Antibiot. and Chemother. 9, 722 (1959).
Warburg, O.: tJber den Stoffwechsel der Tumoren. Berlin 1926.
Webb, J. S., D. B. Cosulich, J. H. Mowat, J. B. Patrick, R. W. Broschard, W. E. Meyer, R. P. Williams, C. F. Wolf, W. Fulmor, C. Pidacks and J. E. Lancaster: The structures of mitomycins A, B and C and porfiromycin. Part I. J. Amer. chem. Soc. 84, 3185 (1962); — Part II. J. Amer. chem. Soc. 84, 3187 (1962).
Weissbach, H., and E. Katz: Studies on the biosynthesis of actinomycin: Enzymic synthesis of the phenoxazone chromophore. J. biol. Chem. 236, PC 16 (1961).
Welch, A. D.: The problem of drug resistance in cancer chemotherapy. Cancer Res. 19, 359 (1959).
Welsch, M.: Production of actinomycin or a closely related substance by a species of streptomyces distinct from the streptomyces antibioticus of Waksman and Woodruff. Bull. Soc. Chim. biol. (Paris) 28, 557 (1946).
Werkheiser, W. C.: Specific binding of 4-amino folic acid analogues by folic acid reductase. J. biol. Chem. 286, 888 (1961).
Whitelocks, O. ST. V.: Genetic concept for the origin of cancer. Ann. N. Y. Acad. Sci. 71, art. 6, 807–1241 (1958).
Wilmanns, W.: Zum Wirkungsmechanismus von 6-mercaptopurin. Klin. Wschr. 40, 1170 (1962).
Wissemann, C. L. jr., F. E. Hahn, H. Hopps and J. E. Smadel: Chloramphenicol inhibition of protein synthesis. Fed. Proc. 12, 466 (1953).
Woodruff, H. B., and S. A. Waksman: Historical Background. Ann. N. Y. Acad. Sci. 89, 287 (1960).
Wright, J. C., V. B. Dolgopol, M. Logan, A. Prigot and L. T. Wright: Clinical evaluation of puromycin in human neoplastic disease. Arch, intern. Med. 96, 61 (1955).
Yamamoto, T., S. Yamaoko, H. Umezawa, T. Takeuchi and K. Nitta: Antitumor effects of sarkomycin. Gann 45, 503 (1954).
Yarmolinsy, M. B., and G. L. De La Haba: Inhibition by puromycin of amino acid incorporation into protein. Proc. Nat. Acad. Sci. 45, 1721 (1959).
Zakrzewski, S. F., and C. A. Nichol: Evidence for a single enzyme reducing folate and dihydrofolate. J. biol. Chem. 235, 2984 (1961).
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Schmidt, C.G. (1963). Cytostatische Antibiotica. In: Heilmeyer, L., Schoen, R., De Rudder, B., Prader, A. (eds) Ergebnisse der Inneren Medizin und Kinderheilkunde. Ergebnisse der Inneren Medizin und Kinderheilkunde, vol 20. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-94862-6_8
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