Skip to main content

Part of the book series: Ergebnisse der Inneren Medizin und Kinderheilkunde ((KINDERHEILK. NF,volume 20))

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.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 44.99
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 59.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

Literatur

  1. Abraham, E. P., and G. G. F. Newton: Chemistry and classification of antibiotics. Brit. med. Bull. 16, 3 (1960).

    PubMed  CAS  Google Scholar 

  2. 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).

    Article  CAS  Google Scholar 

  3. Albrich, E., U. P. Hefel: Zur Behandlung eines multiplen Myeloms (Gamma-Plasmo- cytom) mit Actinomycin C. (Sanamycin). Med. Klin. 51, 469 (1956).

    CAS  Google Scholar 

  4. Alder, A., U. F. Zbinden: Zur Therapie des Lymphogranuloms. (Morbus Hodgkin). Schweiz, med. Wschr. 83, 924 (1953).

    CAS  Google Scholar 

  5. 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).

    Google Scholar 

  6. 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).

    PubMed  CAS  Google Scholar 

  7. 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).

    CAS  Google Scholar 

  8. Back, N, and E. Feltz: Zitiert bei N. Back, R. R. Shields and A. E. Munson: Antibiot. and Chemother. 11, 652 (1961).

    CAS  Google Scholar 

  9. 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.

    Google Scholar 

  10. 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).

    Article  PubMed  CAS  Google Scholar 

  11. Balassa, J.: Action de la mitomycine C sur la transformation du pneumocoque. Ann. Inst. Pasteur 102, 547 (1962).

    CAS  Google Scholar 

  12. 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).

    Article  CAS  Google Scholar 

  13. 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).

    Article  CAS  Google Scholar 

  14. Bases, R. E.: Modification of the radiation response determined by single-cell technics: Actinomycin D. Cancer Res. 19, 1233 (1959).

    Google Scholar 

  15. Begemann, H.: Clinical experience with actinomvcin c. Ann. N. Y. Acad. Sci. 89, 454 (1960).

    Article  PubMed  CAS  Google Scholar 

  16. Begemann, H. Que peut-on attendre de l’actinomycine dans les maladies cancereuses ou paracancereuses ? J. Therap. Paris 1955.

    Google Scholar 

  17. 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.

    Google Scholar 

  18. 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).

    Article  CAS  Google Scholar 

  19. 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).

    Article  CAS  Google Scholar 

  20. 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.

    Google Scholar 

  21. Bertino, J. R., B. W. Gabrio and F. M. Huennekens: Dihydrofolic reductase in human leucemic leucocytes. Biochim. biophys. Acta Res. Commun. 3, 461 (1961).

    Article  Google Scholar 

  22. 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).

    Google Scholar 

  23. 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).

    PubMed  CAS  Google Scholar 

  24. Bierling, R.: Die Wirkung von Actinomycinen auf menschliche Gewebe in vitro. Z. Krebsforsch. 63, 519 (1960).

    Article  CAS  Google Scholar 

  25. Bloemendal, H., U. Z. Littauer and V. Daniel: Transfer of soluble polynucleotides to microsomal RNA. Biochim. biophys. Acta (Amst.) 51, 66 (1961).

    Article  CAS  Google Scholar 

  26. 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).

    Google Scholar 

  27. Bollag, W., U. A. F. Esselier: Erfahrungen mit Actinomycin C. Schweiz, med. Wschr. 84, 1174 (1954).

    CAS  Google Scholar 

  28. Börnstein, R., U. F. Stein: Anatomische Heilung einer Lymphogranulomatose nach Actinomycintherapie. Ärztl. Wschr. 9, 896 (1954).

    Google Scholar 

  29. 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).

    Article  CAS  Google Scholar 

  30. 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).

    PubMed  CAS  Google Scholar 

  31. 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).

    Google Scholar 

  32. 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.

    Google Scholar 

  33. 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).

    PubMed  CAS  Google Scholar 

  34. 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).

    Article  Google Scholar 

  35. 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).

    Google Scholar 

  36. Brockmann, H., u. M. Grtjbhofer: Actinomycin; Zur Kenntnis des Actinomycin C. Naturwissenschaften 36, 376 (1949); 37, 494 (1950).

    Article  CAS  Google Scholar 

  37. 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).

    Google Scholar 

  38. Brockmann, H, u. H. Muxfeldt: Konstitution und Synthese des Actinomycin. Angew. Chem. 68, 67 (1956).

    Google Scholar 

  39. Brockmann, H, u. B. Franck: Hydrierende Acetylierung von Actinomycinen. Aufspaltung der Actinomycine zu Actinomycinsäuren. Angew. Chem. 68, 68 (1956).

    Google Scholar 

  40. Brockmann, H, u. H. Muxfeldt: Konstitution und Synthese des Actinomvcin-Chromophors. Angew. Chem. 68, 69 (1956).

    Article  CAS  Google Scholar 

  41. Brockmann, H, G. Bohnsack, B. Franck, H. Grone, H. Muxfeldt u. C. Süling: Bilanz der Actinomycin C3-Abbauprodukte. Angew. Chem. 68, 70 (1956).

    Google Scholar 

  42. Brockmann, H, u. J. H. Manegold: Überführung von Actinomycin X2 in Actinomycin XJ. Natur-wissenschaften 45, 310 (1958).

    Google Scholar 

  43. Brockmann, H, u. H. Muxfeldt: Konstitution und Synthese des Actinomycin-Chromophors. Chem. Ber. 91, 1242 (1958).

    Article  CAS  Google Scholar 

  44. Brockmann, H, G. Pampus U. J. H. Manegold: ActinomycinX0ß; zur Systematik und Nomenklatur der Actinomycine. Chem. Ber. 92, 1294 (1959).

    Article  CAS  Google Scholar 

  45. Brockmann, H, Structural differences of the actinomycins and their derivatives. Ann. N. Y. Acad. Sci. 89, 323 (1960).

    Article  Google Scholar 

  46. Brunsch, K. H., U. J. Nevinny-Stickel: Über die Lymphogranulomatose im Bereich der Weiblichen Geschlechtsorgane. Arch. Gynäk. 188, 215 (1957).

    Article  Google Scholar 

  47. 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).

    PubMed  CAS  Google Scholar 

  48. Buchanan, J. M., Enzymatic synthesis of purine nucleotides. Harvey Lect. 54, 104 (1958/59).

    Google Scholar 

  49. Bullock, E., and A. W. Johnson: Actinomycin V. The structure of actinomycin D. J. chem. Soc. 1957, 3280.

    Google Scholar 

  50. 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).

    Article  PubMed  CAS  Google Scholar 

  51. Businco, L.: Actinomycin C, anaphylaxie allergie. Presse med. 1955, 1687.

    Google Scholar 

  52. Butenandt, A., W. Weidel U. E. Becker: Kynurenin als Augenpigmentbildung auslösendes Agens bei Insekten. Naturwissenschaften 28, 63 (1940).

    Article  CAS  Google Scholar 

  53. Butenandt, A. Biochemische Untersuchungen zur Wirkungsweise der Erbfaktoren. Angew. Chem. 61, 262 (1949).

    Article  Google Scholar 

  54. 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).

    Article  CAS  Google Scholar 

  55. Butenandt, A Biochemische Beiträge zur Insektenphysiologie. Gesellschaft Physiol. Chem. 20–22.9.1954 (Kiel).

    Google Scholar 

  56. 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).

    Google Scholar 

  57. Butenandt, A. U. G. Neubert: Über Ommochrome. V. Mitt.: Xanthommatin, ein Augenfarbstoff der Schmeißfliege, Calciphora erythrocephala. Hoppe-Seylers Z. physiol. Chem. 301, 109 (1955).

    Google Scholar 

  58. Butenandt, u. R. Beckmann: Über Ommochrome. VI. Mitt.: Zur Genese von Rhodommatin und Ommatin C. Hoppe-Seylers Z. physiol. Chem. 301, 115 (1955).

    Google Scholar 

  59. 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).

    Google Scholar 

  60. 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).

    Google Scholar 

  61. 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).

    Article  CAS  Google Scholar 

  62. Butenandt, U, R. Beckmann, Wirkstoffe des Insektenreiches. Naturwissenschaften 46, 461 (1959).

    Article  CAS  Google Scholar 

  63. Caputo, A., B. Giovanella and R. Giuliano: Antitumoral action of new sarcomycin derivatives. Nature (Lond.) 190, 819 (1961).

    Article  CAS  Google Scholar 

  64. 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).

    PubMed  CAS  Google Scholar 

  65. 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).

    Google Scholar 

  66. 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.

    Google Scholar 

  67. 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).

    Google Scholar 

  68. 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).

    Google Scholar 

  69. 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).

    CAS  Google Scholar 

  70. 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.

    Google Scholar 

  71. 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).

    CAS  Google Scholar 

  72. Cohen, S. S., and H. Barner: Unbalanced growth in escherichia coli. Proc. nat. Acad. Sci. (Wash.) 40, 385 (1954).

    Google Scholar 

  73. 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.

    Google Scholar 

  74. 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).

    Google Scholar 

  75. Cornman, I.: Survival of normal cells in penicillin solutions lethal to malignant cells. Science 99, 247 (1944).

    Article  PubMed  CAS  Google Scholar 

  76. Craveri, R., U. G. V. Veronesi: Wirkung von Actinomycin auf die Mitose. Nature (Lond.) 179, 1306 (1957).

    Article  CAS  Google Scholar 

  77. Croizat, P.: Essais thérapeutiques concernant l’actinomycine C. Presse méd. 62, 738 (1954).

    PubMed  CAS  Google Scholar 

  78. 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.

    Google Scholar 

  79. Dagg, C. P., and D. A. Karnofsky: Teratogenic effects of azaserine on the chick embryo. J. exper. Zool. 130, 555 (1955).

    Article  CAS  Google Scholar 

  80. Dalgliesh, C. E., and A. R. Todd: Actinomycin. Nature (Lond.) 164, 830 (1949).

    Article  Google Scholar 

  81. Dalgliesh, C. E., A. W. Johnson, A. R. Todd and L. C. Vining: Actinomycin. I. Amino acid content. J. chem. Soc. 1950, 2946.

    Google Scholar 

  82. D’angio, G. J., S. Farber and C. L. Maddock: Potention of X-ray effects by actinomycin D. Radiology 73, 175 (1959).

    PubMed  Google Scholar 

  83. 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).

    PubMed  CAS  Google Scholar 

  84. 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.

    Google Scholar 

  85. 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).

    Google Scholar 

  86. 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).

    Article  CAS  Google Scholar 

  87. Di Paolo, J. A., G. E. Moore and T. F. Niedbala: Experimental studies with actinomycin D. Cancer Res. 17, 1127 (1957).

    Google Scholar 

  88. Di Paolo, J. A., Experimental evaluation of actinomycin D. Ann. N. Y. Acad. Sci. 89, 408 (1960).

    Article  Google Scholar 

  89. Doerr, W., U. F. Stein: Therapeutisch bedingte Pathomorphose. Münch, med. Wschr. 1954, 660.

    Google Scholar 

  90. 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).

    Article  PubMed  CAS  Google Scholar 

  91. Domagk, G.: Welche Erkenntnisse über den Krebs vermittelt uns die experimentelle Krebsforschung? Münch, med. Wschr. 1952, 1841.

    Google Scholar 

  92. 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 ).

    Google Scholar 

  93. Eble, T. E., H. Hoeksema, G. A. Boyack and G. M. Savage: Psicofuranine. I. Discovery, isolation and properties. Antibiot. and Chemother. 9, 419 (1959).

    CAS  Google Scholar 

  94. 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).

    CAS  Google Scholar 

  95. 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).

    CAS  Google Scholar 

  96. 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).

    Article  PubMed  CAS  Google Scholar 

  97. 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 ).

    Google Scholar 

  98. Evans, J. S., and J. E. Gray: Psicofuranine. VI. Antitumor and toxicopathological studies. Antibiot. and Chemother. 9, 675 (1959).

    CAS  Google Scholar 

  99. Evans, A. E.: Mitomycin C. Cancer Chemother. Rep. 14, 1 (1961).

    PubMed  CAS  Google Scholar 

  100. Evans, J. S., A. E. Musser and J. E. Gray: Porfiromycin antitumor and toxicopathologic studies. Antibiot. and Chemother. 11, 445 (1961).

    CAS  Google Scholar 

  101. Farber, S.: Clinical and biological studies with actinomycins. IN: Amino acids and peptides with antimetabolitic activity. Boston: Little Brown. 1958 — Geigy-Symp. S. 138.

    Google Scholar 

  102. Farber, S., Current clinical and experimental studies in cancer chemotherapy. Unio Internat, contra cancrum. Tokyo p. 42 (1960).

    Google Scholar 

  103. 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).

    Article  PubMed  CAS  Google Scholar 

  104. 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).

    PubMed  CAS  Google Scholar 

  105. 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.

    Google Scholar 

  106. Field, J. B., F. Costa, A. Boryczka: Origin of a new antitumor agent, streptovitacin. Antibiot. Ann. S. 547 ( Medical Encyclopedia N. Y. 1959 ).

    Google Scholar 

  107. 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 ).

    Google Scholar 

  108. 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).

    Google Scholar 

  109. 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).

    Google Scholar 

  110. E. Dolendo and A. Mireless: Preliminary canine and clinical evaluation of a new antitumor agent, streptovitacin A. Clin. Res. 8, 134 (1960).

    Google Scholar 

  111. Fischer, G. A.: Nutritional and amethopterin-resistant characteristics of leukemic clones. Cancer Res. 19, 372 (1959).

    PubMed  CAS  Google Scholar 

  112. Fischer, G. A.: Increased levels of folic acid reductase as a mechanism of resistance to amethopterin in leukemic cells. Biochem. Pharmacol. 7, 75 (1961).

    Article  PubMed  CAS  Google Scholar 

  113. Fleischhacker, H., U. A. Stacher: Wert und Wirkung der Zytostatika bei malignen lymphatischen Systemerkrankungen. Wien. Z. inn. Med. 43, 200 (1962).

    PubMed  CAS  Google Scholar 

  114. Foulds, L.: Neoplastic development. Johns Hopk. Hosp. Bull. 1958, 680.

    Google Scholar 

  115. Frank, W., and A. E. Osterberg: Mitomycin C, the evaluation of the japanese reports. Cancer Chemother. Rep. 9, 114 (1960).

    PubMed  CAS  Google Scholar 

  116. 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).

    Article  PubMed  CAS  Google Scholar 

  117. 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).

    Article  CAS  Google Scholar 

  118. 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).

    Article  CAS  Google Scholar 

  119. Garattini, S., V. Costa, B. Murelli, V. Palma e N. Vegeto: G. ital. Chemioter. 3, 498 (1956).

    PubMed  CAS  Google Scholar 

  120. Gasperini, G.: Recherches morphologiques et biologiques sur un microorganisme du l’atmosphère. Ann. Microgr. 10, 449 (1890).

    Google Scholar 

  121. 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.

    Google Scholar 

  122. Gellhorn, A., and E. Hirschberg: Investigations of diverse systems for cancer chemotherapy screening. Cancer Res. Suppl. Nr. 3 (1955).

    Google Scholar 

  123. Gernez-Rieux, CH., et M. Goudemand: Premiers résultats de l’emploi de l’actinomycine C en thérapeutique. Presse méd. 62, 739 (1954).

    PubMed  CAS  Google Scholar 

  124. 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).

    Google Scholar 

  125. 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).

    Google Scholar 

  126. 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).

    Article  CAS  Google Scholar 

  127. Goldberg, I. H, and M. Rabinowitz: Actinomycin D inhibition of deoxyribonucleic acid-dependent synthesis of ribonucleic acid. Science 136, 315 (1962).

    Article  PubMed  CAS  Google Scholar 

  128. Goldin, A., and N. Mantel: The employment of combinations of drugs in the chemotherapy of neoplasma: A review. Cancer Res. 17, 635 (1957).

    PubMed  CAS  Google Scholar 

  129. 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).

    Article  PubMed  CAS  Google Scholar 

  130. 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).

    Article  CAS  Google Scholar 

  131. 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).

    Google Scholar 

  132. Greenlees, J., and G. A. Le Page: Purine biosynthesis and inhibitors in ascites cell tumors. Cancer Res. 16, 808 (1956).

    PubMed  CAS  Google Scholar 

  133. 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).

    PubMed  CAS  Google Scholar 

  134. 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).

    Google Scholar 

  135. Gröner, H.: Zur Chemie der Actinomycine. 4. Nat. Kongress für Chemotherapie. Rom 1956.

    Google Scholar 

  136. Grubhofer, N.: Neue Apparatur zur fraktionierten Gegenstromverteilung zwischen zwei Flüssigkeiten. Chem.-Ing.-Techn. 22, 209 (1950).

    Article  CAS  Google Scholar 

  137. Hackethal, C. A., and R. B. Cölbe Y: Preliminary clinical study of streptonigrin in neoplastic disease. Proc. Amer. Ass. Cancer Res. 3, 115 (1960).

    Google Scholar 

  138. Hackmann, CH.: Experimentelle Untersuchungen über die Wirkung von Actinomycin C (HBF 386) bei bösartigen Geschwülsten. Z. Krebsforsch. 58, 607 (1952).

    Article  PubMed  CAS  Google Scholar 

  139. Hackmann, CH.: HBF 386 (Actinomycin C) ein cytostatisch wirksamer Naturstoff. Strahlentherapie 90, 297 (1953).

    Google Scholar 

  140. Hackmann, CH.: Les recherches expérimentales sur le cancer. Rev. Progrès Thérap. 23, 64 (1954).

    Google Scholar 

  141. Hackmann, CH.: Untersuchungen über den Einfluß des Sanamycin (Actinomycin C) auf tierische Organe: Milz, Thymus, Lymphknoten, Nebennieren und Keimdrüsen. Z. Krebsforsch. 60, 250 (1954).

    Article  PubMed  CAS  Google Scholar 

  142. Hackmann, CH.: Stoffwechselprodukte aus Mikroorganismen (Antibiotika) als antineo plastische Wirkstoffe. Dtsch. med. Wschr. 80, 812 (1955).

    Article  PubMed  CAS  Google Scholar 

  143. Hackmann, CH., u. G. Schmidt-Kastner: Über die cytostatische Wirkung verschiedener neuer bio-synthetischer Actinomycine bei experimentellen Tumoren. Z. Krebsforsch. 61, 607 (1957).

    Article  PubMed  CAS  Google Scholar 

  144. Hackmann, CH.: Der zytostatische Effekt antibiotischer Wirkstoffe. Krebsforsch, u. Krebsbekämpf. 3, 333 (1959).

    Google Scholar 

  145. Hackmann, CH.: Berliner Symposium 1959. S. 329. Berlin: Akademie Verlag 1960.

    Google Scholar 

  146. Haensch, R.: Elektrophoretische Serumuntersuchungen bei Lymphogranulomatose - Patienten unter der Sanamycin-Behandlung. Z. Haut- u. Geschl.-Kr. 21, 269 (1956).

    CAS  Google Scholar 

  147. 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).

    Google Scholar 

  148. Hanka, L. J.: Mechanism of action of psicofuranine. J. Bact. 80, 30 (1960).

    PubMed  CAS  Google Scholar 

  149. Hackmann, CH.: Porfiromycin, a new antibiotic. IV. Microbiological assays. Conference on antimicrobial agents. October, 26–28, 1960 Washington.

    Google Scholar 

  150. Hara, T.: Preparation of sarcomycin derivatives. Cancer ehem. Abstr. 1, 4095 (1960).

    Google Scholar 

  151. Harbers, E., and W. Mueller: On the inhibition of RNA synthesis by actinomycin. Biochem. biophys. Res. Commun. 7, 107 (1962).

    Article  PubMed  CAS  Google Scholar 

  152. 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).

    Article  CAS  Google Scholar 

  153. 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).

    CAS  Google Scholar 

  154. 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).

    CAS  Google Scholar 

  155. Hata, T., A. Matsumae, K. Owada and Y. Sano: Studies on the treatment of experimental infections. Chemother. Rev. 4, 295 (1956).

    Google Scholar 

  156. Heckner, F., J. Hamm U. W. Eger: Cytologische Kriterien der Wirkung von Sanamycin. Klin. Wschr. 35, 459 (1957).

    Article  PubMed  CAS  Google Scholar 

  157. 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).

    Google Scholar 

  158. 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).

    PubMed  CAS  Google Scholar 

  159. 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).

    Google Scholar 

  160. Herr, R. R.: Structures of streptovitacins. Amer. J. chem. Soc. 81, 2595 (1959).

    Article  CAS  Google Scholar 

  161. 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.

    Google Scholar 

  162. 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).

    Article  CAS  Google Scholar 

  163. 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.

    Google Scholar 

  164. Hirata, Y., and K. Nakaniski: Antibiotic substance from Actinomyces flavus. J. Antibiot. (Tokyo) 2, 189 (1948).

    Google Scholar 

  165. Hirata, Y., and K. Nakaniski: Actinomycin J2, a by-product from a strain of actinomyces. Bull. Soc. chem. Japan 22, 121 (1949).

    Article  CAS  Google Scholar 

  166. 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).

    PubMed  CAS  Google Scholar 

  167. Holzer, E., U. H. Kröger: Zum carcinostatischen Wirkungsmechanismus von Äthylen - imin-Verbindungen. Biochem. Z. 330, 579 (1958).

    PubMed  CAS  Google Scholar 

  168. Holzer, E., P. Glogner U. G. Sedlmayer: Zum Mechanismus der Glykolysehemmung durch carcinostatisch wirkende Äthylenimin-Verbindungen. Biochem. Z. 330, 59 (1958).

    PubMed  CAS  Google Scholar 

  169. Holzer, E., u. H. J. Boltze: Über die Wirkung von Nicotinsäureamid auf die Glykolysehemmung von Ascitestumorzellen durch Äthylenimin-Verbindungen. Z. Krebsforsch. 64, 113 (1961).

    Google Scholar 

  170. 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).

    PubMed  CAS  Google Scholar 

  171. 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).

    CAS  Google Scholar 

  172. 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).

    PubMed  Google Scholar 

  173. Hübener, H. J.: Die physiologische Funktion der Nebennierenrinden-Hormone als Enzym-Induktoren. Dtsch. med. Wschr. 87, 438 (1962).

    Article  Google Scholar 

  174. Huennekens, F. M., M. J. Osborn and H. R. Whiteley: Folic acid coenzymes. Science 128, 120 (1958).

    Article  PubMed  CAS  Google Scholar 

  175. Huggins, C.: Hormonabhängige Geschwülste—klinisch und experimentell. Klin. Wschr. 1958, 1102; Ann. Surg. 115, 1191 (1942).

    Google Scholar 

  176. 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).

    CAS  Google Scholar 

  177. Huguenin, R., R. Truhaut et J. S. Bourdin: Experimentation de l’actinomycine. Presse méd. 62, 740 (1954).

    PubMed  CAS  Google Scholar 

  178. 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).

    Article  PubMed  CAS  Google Scholar 

  179. 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).

    CAS  Google Scholar 

  180. Hurley, J. D., E. H. Ellison, J. Riesch and W. Schulte: Chemotherapy of solid carcinoma. J. Amer. med. Ass. 174, 1696 (1960).

    Article  CAS  Google Scholar 

  181. Hutchings, B. L.: Ciba Foundation Symp. 1957, Chemistry and Biology of Purines. S. 177.

    Google Scholar 

  182. Iijima, T., and A. Hagiwara: Mutagenic action of mitomycin C on escherichia coli. Nature (Lond.) 185, 395 (1960).

    Article  CAS  Google Scholar 

  183. 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).

    Google Scholar 

  184. Ishihara, T.: Clinical experience with carzinophilin. Rinsho Fujinka Sanka 12, 58 (1958).

    Google Scholar 

  185. Ishu, Y.: Anti-cancerous effect of carzinophilin. Asian med. J. 1, 34 (1958).

    Google Scholar 

  186. 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).

    Google Scholar 

  187. Ishiyama, S.: Clinical observations of some malignant tumors treated with sarcomycin, a new antitumor antibiotic. J. Antibiot. Ser. A 7, 82 (1954).

    CAS  Google Scholar 

  188. Iwataru, M.: Method of preparing sarcomycin-urotropine compounds. Cancer Chemother. Abstr. 1, 4340 (1961).

    Google Scholar 

  189. 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).

    PubMed  CAS  Google Scholar 

  190. 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).

    CAS  Google Scholar 

  191. 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).

    PubMed  CAS  Google Scholar 

  192. Jacquez, J. A., and J. H. Sherman: Enzymatic degradation of azaserine. Cancer Res. 22, 56 (1962).

    PubMed  Google Scholar 

  193. 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).

    PubMed  CAS  Google Scholar 

  194. Jagger, D. V., N. M. Kredich and A. J. Guarino: Inhibition of Ehrlich ascites tumor growth by cordycepin. Cancer Res. 21, 216 (1961).

    PubMed  CAS  Google Scholar 

  195. Janbon, M.: Premier résultats de l’application de l’actinomycine C en thérapeutique. Presse Méd. 62, 741 (1954).

    PubMed  CAS  Google Scholar 

  196. Johne, H. 0., u. A. Kroher: Über die Behandlung der Lymphogranulomatosis maligna (Hodgkin-Sternberg) mit Actinomycin C. Dermatologica (Basel) 109, Nr. 5 (1954).

    Google Scholar 

  197. Johnson, A. W.: Actinomycin. Spec. Publ. chem. Soc. 5, 82 (1956).

    Google Scholar 

  198. Johnson, A. W., and A. Mauger: The isolation and structure of actinomycins II and III. Biochem. J. 73, 535 (1959).

    PubMed  CAS  Google Scholar 

  199. 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).

    Google Scholar 

  200. Jones jr., R.: Mitomycin C. A preliminary report of studies of human pharmacology and initial therapeutic trial. Cancer Chemother. Rep. 2, 7 (1959).

    Google Scholar 

  201. 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).

    PubMed  CAS  Google Scholar 

  202. 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).

    CAS  Google Scholar 

  203. 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).

    Google Scholar 

  204. Amination of uridine nucleotides to cytidine nucleotides by soluble mammalian enzymes: Role of glutamine and guanosine nucleotides. Biochim. biophys. Acta (Amst.) 30, 195 (1958).

    Google Scholar 

  205. Kanamori, H., T. Shima, C. Morita and T. Hata: Studies on antitumor activity of mitomycin. J. Antibiot. (Tokyo) 10, 120 (1957).

    CAS  Google Scholar 

  206. Kaplan, L.: Studies on the action of azaserine on escherichia coli. ph. D. Thesis, Cornell Univ. 1957.

    Google Scholar 

  207. Katz, E., and W. A. Goss: Influence of amino-acids on actinomycin biosynthesis. Nature (Lond.) 182, 1668 (1958).

    Article  CAS  Google Scholar 

  208. Katz, E., and W. A. Goss: Controlled biosynthesis of actinomycin with sarcosine. Biochem. J. 73, 458 (1959).

    PubMed  CAS  Google Scholar 

  209. Katz, E.: Biogenesis of the actinomycins. Ann. N. Y. Acad. Sci. 89, 304 (1960).

    Article  PubMed  CAS  Google Scholar 

  210. 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).

    Google Scholar 

  211. Kawamata, J., and H. Fujita: Separations and characterization of actinomycin that contains alloisoleucine. Med. J. Osaka Univ. 8, 743 (1958).

    CAS  Google Scholar 

  212. Kawamata, J., N. Nakabayashi, A. Kawai and T. Ushida: Experimental production of mode of action of actinomycin. Med. J. Osaka Univ. 8, 753 (1958).

    Google Scholar 

  213. Kawamata, J., N. Nakabayashi, A. Kawai and H. Fujita: Studies on the carcinogenic effect of actinomycin. Biken’s J. 2, 105 (1959).

    CAS  Google Scholar 

  214. Kawamata, J., N. Nakabayashi:Experimental production of sarcoma in mice with actinomycini. Gann 50, Suppl. 126 (1959).

    Google Scholar 

  215. Kawamata, J., and M. Imanishi: Interaction of actinomycin with deoxyribonucleic acid. Nature (Lond.) 187, 1112 (1960).

    Article  CAS  Google Scholar 

  216. Kawamata, J. H. Fujita and A. Ikegami: Anticancer effect of actinomycinic acid. J. Antibiot. (Tokyo) Ser. A 13, 415 (1960).

    CAS  Google Scholar 

  217. 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).

    CAS  Google Scholar 

  218. Kersten, H., and H. M. Rauen: Degradation of deoxyribonucleic acid in escherichia coli cells treated with mitomycin C. Nature (Lond.) 190, 1195 (1961).

    Article  CAS  Google Scholar 

  219. Kersten, H. Action of Mitomycin C in nucleic acid metabolism in tumor and bacterial cells. Biochim. biophys. Acta (Amst.) 55, 558 (1962).

    Google Scholar 

  220. 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).

    Article  CAS  Google Scholar 

  221. Kersten, W.: Interaction of actinomycin C with constituents of nucleic acids. Biochim. biophys. Acta (Amst.) 47, 610 (1961).

    Article  CAS  Google Scholar 

  222. Kersten, W., u. H. Kersten: Zur Wirkungsweise von Actinomycinen. II. Bildung überschüssiger Desoxyribonucleinsäure in Bacillus subtilis. Hoppe-Seylers. Z. physiol Chem. 327, 234 (1962).

    Article  CAS  Google Scholar 

  223. Kersten, W. Biologische Wirkung, klinische Bedeutung und biochemischer WTirkungsmechanismus der Actinomycine. Habilitations-Schrift, Univ. Münster 1962.

    Google Scholar 

  224. Kirk, J. M.: The mode of action of actinomycin D. Biochim. biophys. Acta (Amst.) 42, 167 (1960).

    Article  CAS  Google Scholar 

  225. 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).

    Google Scholar 

  226. Kondo, T.: Adverse effects of cancer chemotherapy. 8. Internat. Krebscongress, Moskau 1962, S. 321.

    Google Scholar 

  227. Korst, D. R., and O. O. Meyer: Negative effect of actinomycin D treatment in three cases of Hodgkins disease. Antibiot. Med. 1, 474 (1955).

    PubMed  CAS  Google Scholar 

  228. 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).

    Google Scholar 

  229. Kröger, H., B. Ulrich U. H. Holzer: Wirkung carcinostatischer Verbindungen auf die Konzentration von Diphosphopyridinnucleotid in Tumoren. Arzneimittel-Forsch. 9, 598 (1959).

    Google Scholar 

  230. 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).

    Article  PubMed  CAS  Google Scholar 

  231. Lehr, H., and J. Berger: The isolation of a crystalline actinomycin-like antibiotic. Arch. Biochem. 23, 503 (1949).

    PubMed  CAS  Google Scholar 

  232. 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).

    Article  Google Scholar 

  233. 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).

    PubMed  CAS  Google Scholar 

  234. 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.

    Google Scholar 

  235. 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).

    Google Scholar 

  236. Lindenbein, W.: Über einige interessante Aktinomycetenstämme und ihre Klassifizierung. Arch. Mikrobiol. 17, 361 (1952).

    Article  Google Scholar 

  237. 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).

    PubMed  CAS  Google Scholar 

  238. Lowery, O. E., and J. W. Foster: Bacterial screening of culture filtrates for synergism with selected anticancer compounds. Antibiot. and Chemotherap. 9, 232 (1959).

    CAS  Google Scholar 

  239. Lukens, L. N., and K. A. Herrington: Enzymic formation of 6-mercaptopurineribotide. Biochim. biophys. Acta (Amst.) 24, 432 (1957).

    Article  CAS  Google Scholar 

  240. 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).

    Article  PubMed  CAS  Google Scholar 

  241. Magee, W. E., and F. S. Eberts jr.: Studies with psicofuranine in the tumor-bearing rat. Cancer Res. 21, 611 (1961).

    PubMed  CAS  Google Scholar 

  242. 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).

    PubMed  Google Scholar 

  243. Magnus, D., U. K. H. Zeitler: Kombination von Röntgenstrahlen und Sanamycin bei der Behandlung von Erkrankungen des blutbildenden Systems. Strahlentherapie 98, 413 (1955).

    PubMed  CAS  Google Scholar 

  244. Marino, S., in S. Shiba and T. Taguchi: Study on Mitomycin C, N. 101 (1959), Osaka Univ.

    Google Scholar 

  245. 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).

    Google Scholar 

  246. Marquart, H., U. E. Glass: Die Chromosomenzahlen in den Leberzellen von Ratten verschiedenen Alters. Chromosoma 8, 617 (1957).

    Article  Google Scholar 

  247. 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).

    Google Scholar 

  248. Streptonigrin, an antitumor agent produced by strains of streptomyces flocculus: I. Microbiological studies. Antibiot. and Chemother. 11, 151 (1961).

    Google Scholar 

  249. Martin, R., et J. P. Munier: Premiers résultats de 12 maladies de Hodgkin traitées par l’actinomycine C. Presse méd. 62, 741 (1954).

    PubMed  CAS  Google Scholar 

  250. Martin, H.: Erfahrungen bei der Behandlung der Lymphogranulomatose mit Actinomycin C. (Sanamycin) Klin. Wschr. 32, 518 (1954).

    Article  PubMed  CAS  Google Scholar 

  251. 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).

    Google Scholar 

  252. 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.

    Google Scholar 

  253. 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).

    Google Scholar 

  254. 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).

    CAS  Google Scholar 

  255. Merz, T.: Effect of mitomycin C on lateral root-tip chromosomes of vicia faba. Science 133, 329 (1961).

    Article  PubMed  CAS  Google Scholar 

  256. Miller, E., and R. D. Sullivan: Clinical effects of the continuous intravenous infusion of cancer chemotherapeutic compounds. 8. Internat. Krebscongress, Moskau 1962, S. 338.

    Google Scholar 

  257. 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).

    Google Scholar 

  258. 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).

    Google Scholar 

  259. 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.

    Google Scholar 

  260. 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).

    Article  CAS  Google Scholar 

  261. Moore, E. C., and G. A. Le Page: In vivo sensitivity of normal and neoplastic mouse tissues to azaserine. Cancer Res. 17, 804 (1957).

    PubMed  CAS  Google Scholar 

  262. Moore, G. E., T. Kondo and J. Badillo: Clinical trial of actinomycin D. Proc. Amer. Ass. Cancer Res. 2, 328 (1958).

    Google Scholar 

  263. 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).

    Article  PubMed  CAS  Google Scholar 

  264. 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).

    PubMed  CAS  Google Scholar 

  265. 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).

    Article  CAS  Google Scholar 

  266. 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).

    Article  CAS  Google Scholar 

  267. Mühlbock, O.: Der Einfluß von Hormonen auf den Tumor. Klin. Med. 3, 355 (1960). ( Berliner Symp. Carcinogenese Dez. 1959 ).

    Google Scholar 

  268. 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).

    Article  PubMed  CAS  Google Scholar 

  269. Nakata, A., M. Sekiguchi and J. Kawamata: Inhibition of multiplication of bacteriophage by actinomycin. Nature (Lond.) 189, 246 (1961).

    Article  CAS  Google Scholar 

  270. 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).

    Article  Google Scholar 

  271. 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).

    PubMed  CAS  Google Scholar 

  272. 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).

    Article  CAS  Google Scholar 

  273. 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).

    PubMed  CAS  Google Scholar 

  274. Nichol, C. A., and A. D. Welch: On the mechanism of action of aminopterin. Proc. Soc. exp. Biol. (N. Y.) 74, 403 (1950).

    CAS  Google Scholar 

  275. Nitsch, W., U. K. Thein: Beitrag zur Behandlung der Lymphogranulomatose mit Sanamycin. Ther. d. Gegenw. 94, 49 (1955).

    CAS  Google Scholar 

  276. 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).

    PubMed  CAS  Google Scholar 

  277. 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).

    Google Scholar 

  278. 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).

    CAS  Google Scholar 

  279. Ohara, T.: The study on the chemotherapy of gastric cancer. Preliminary report. Proc. Jap. Cancer Ass. 19th Meeting 1960, S. 79.

    Google Scholar 

  280. 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).

    Article  Google Scholar 

  281. 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).

    CAS  Google Scholar 

  282. Olmer, J.: Essais de traitement de certains hemopathies malignes par Factinomycme C. Presse med. 62, 742 (1954).

    PubMed  CAS  Google Scholar 

  283. 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).

    CAS  Google Scholar 

  284. Osten, W., u. Zademack: Klinische Erfahrungen mit Sanamycin bei Lymphogranulo-matose. Medizinische 18, 687 (1955).

    PubMed  CAS  Google Scholar 

  285. 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).

    Article  CAS  Google Scholar 

  286. 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).

    Google Scholar 

  287. 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).

    CAS  Google Scholar 

  288. Peters, J. M., and D. M. Greenberg: Studies on folic acid reduction. Biochim. biophys. Acta (Amst.) 32, 273 (1959).

    Article  CAS  Google Scholar 

  289. Philips, F. S., H. S. Schwartz and S. S. Sternberg: Pharmacology of Mitomycin C. I. Toxicity and pathologic effects. Cancer Res. 20, 1354 (1960).

    PubMed  CAS  Google Scholar 

  290. 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).

    Article  PubMed  CAS  Google Scholar 

  291. Pine, E. K.: Concentrative uptake of azaserine by neoplastic plasma cells and lympho¬cytes. J. Nat. Cancer Inst. 21, 973 (1958).

    PubMed  CAS  Google Scholar 

  292. Pinkel, D.: Actinomycin D in childhood cancer. Pediatrics 23, 342 (1959).

    PubMed  CAS  Google Scholar 

  293. 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.

    Google Scholar 

  294. 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).

    Google Scholar 

  295. Potter, V. R.: Sequential blocking of metabolic pathways in vivo. Proc. Soc. exper. Biol. (N. Y.) 76, 41 (1951).

    CAS  Google Scholar 

  296. 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).

    Google Scholar 

  297. Potter, V. R.: The biochemical approach to the cancer Problem. Fed. Proc. 17, 691 (1958)

    PubMed  CAS  Google Scholar 

  298. Preiss, J., and P. Handler: Biosynthesis of diphosphopyridine nucleotide. II. Enzymatic aspects. J. biol. Chem. 233, 493 (1958).

    PubMed  CAS  Google Scholar 

  299. 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).

    PubMed  CAS  Google Scholar 

  300. 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).

    Article  PubMed  CAS  Google Scholar 

  301. Pugh, L. H., E. Katz and S. A. Waksman: Antibiotic and cytostatic properties of the actinomycines. J. Bact. 72, 660 (1956).

    PubMed  CAS  Google Scholar 

  302. 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.

    Google Scholar 

  303. 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.

    Google Scholar 

  304. 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.

    Google Scholar 

  305. Rauen, H. M., H. Kersten U. W. Kersten: Zur Wirkungsweise von Actinomycinen. Hoppe-Seylers Z. physiol. Chem. 321, 139 (1960).

    Article  CAS  Google Scholar 

  306. 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).

    Google Scholar 

  307. Ravina, A., M. Pestel: Die Actinomycine. 30. Cong, franç. méd. Algier 1955. Presse méd. 62, 743 (1954).

    PubMed  CAS  Google Scholar 

  308. 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).

    PubMed  CAS  Google Scholar 

  309. 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).

    Article  PubMed  CAS  Google Scholar 

  310. Reich, E., A. J. Shatkin and E. L. Tatum: Bacteriocidal action of mitomycin C. Biochim. biophys. Acta (Amst.) 53, 132 (1981).

    Article  Google Scholar 

  311. 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).

    Article  PubMed  CAS  Google Scholar 

  312. 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).

    Article  CAS  Google Scholar 

  313. Reilly, H. C., A. Schatz and S. A. Waksman: Antifungal properties of antibiotic substances. J. Bact. 49, 585 (1945).

    PubMed  CAS  Google Scholar 

  314. Reilly, H. C.: Inactivation of azaserine by a liver enzyme. Fed. Proc. 13, 279 (1954).

    Google Scholar 

  315. Reilly, H. C.: The effect of amino acids upon the antimicrobial activity of azaserine. Proc. Amer. Ass. Cancer Res. 1, 40 (1954).

    Google Scholar 

  316. 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).

    Google Scholar 

  317. Reilly, H. C., and K. SUGIURA: An antitumor spectrum of streptonigrin. Antibiot. and Chemother. 11, 174 (1961).

    CAS  Google Scholar 

  318. Riegel, R., U. K. Krückemeyer: Die Behandlung des großfollikulären Lymphoblastoms (M. BriU-Symmers) mit Sanamycin “Bayer”. Ärztl. Wschr. 12, 160 ((957).

    Google Scholar 

  319. Ritter, L.: Die Lymphogranulomatose-Behandlung aus chirurgischer Blickrichtung. Münch, med. Wschr. 96, 1484 (1954).

    CAS  Google Scholar 

  320. Robinson, H. J.: Studies on the toxicity of actinomycin. J. Pharmacol, exp. Ther. 74, 25 (1942).

    CAS  Google Scholar 

  321. Roitt, I. M. I.: The inhibition of carbohydrate metabolism in ascites-tumour-cells by ethyleneimines. Biochem. J. 63, 300 (1956).

    PubMed  CAS  Google Scholar 

  322. 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).

    PubMed  CAS  Google Scholar 

  323. 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).

    CAS  Google Scholar 

  324. Sakai,K.,and T. Teranaka: On antitumor activity of mitomycin against experimental animal tumors. Chemotherap. 5, 222 (1957).

    Google Scholar 

  325. 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).

    Google Scholar 

  326. 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).

    Google Scholar 

  327. 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).

    Google Scholar 

  328. Sartorelli, A. C. The development and biochemical characterization of resistance to azaserine in a TA 3 ascites carcinoma. Cancer Res. 18, 457 (1958).

    PubMed  CAS  Google Scholar 

  329. Sartorelli, A. C. Inhibition of ascites cell growth by combinations of 6-thioguanine and azaserine. Cancer Res. 18, 938 (1958).

    PubMed  CAS  Google Scholar 

  330. Sartorelli, A. C., and B. A. Booth: Antineoplastic activity of combinations of 6-chloropurine and azaserine. Cancer Res. 20, 198 (1960).

    PubMed  CAS  Google Scholar 

  331. 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).

    Google Scholar 

  332. 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).

    CAS  Google Scholar 

  333. 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).

    Google Scholar 

  334. Sayanagi, T.: Med. J. Osaka Univ. 11, 3947 (1959).

    Google Scholar 

  335. 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.

    Google Scholar 

  336. Schmidt, C. G.: Über die Biologische Oxydation und Glykolyse in Tumoren. Klin. Wschr. 1955, 409.

    Google Scholar 

  337. Schmidt, C. G.: Über die Hemmung der Glykolyse von Tumorzellen durch Carcinophilin. Klin. Wschr. 1960, 334.

    Google Scholar 

  338. Schmidt, C. G.: Über den Einfluß von Carcinophilin und Mitomycin C auf die Atmung und Glykolyse von Tumorzellen. Oncologia (Basel) 18, 426 (1960).

    Article  Google Scholar 

  339. 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.

    Google Scholar 

  340. Schmidt, C. G.: Über Beziehungen zwischen DPN(Diphosphopyridinnucleotid) -Konzentration und Glykolysehemmung von Tumorzellen durch Carcinophilin. Z. Krebsforsch. 64, 156 (1961).

    Article  PubMed  CAS  Google Scholar 

  341. Schmidt, C. G.: Beeinflussung des Kohlenhydratstoffwechsels von Tumorzellen durch Carcinophilin. Z. Krebsforsch. 64, 328 (1961).

    Article  PubMed  CAS  Google Scholar 

  342. Schmidt, C. G.: Einfluß von Antibiotica auf den Tumorstoffwechsel. Oncologia (Basel) 15, 144 (1962).

    Article  CAS  Google Scholar 

  343. Schmidt, C. G.: The effect of carcinostatic compounds on carbohydrate metabolism of tumor cells. Extr. Acta Union Internat. Contre Le Cancer 18, 240 (1962).

    CAS  Google Scholar 

  344. Schmidt, H., U. H. Waetin: Über die Behandlung eines metastasierenden Hyper-nephroma mit Sanamycin. Med. Klin. 49, 1369 (1954).

    CAS  Google Scholar 

  345. 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).

    Article  PubMed  CAS  Google Scholar 

  346. Schmidt-Kastner, G.: Über neue biosynthetische Actinomycine. Med. u. Chem. 5, 463 (1956).

    Google Scholar 

  347. Schmidt, C. G., Actinomycin E und F, zwei neue biosynthetische Actinomycingemische. Natur-wissenschaften 43, 131 (1956).

    Google Scholar 

  348. Schmidt, C. G., The production of actinomycins by controlled biosyntheses: The F actinomycins. Ann. N. Y. Acad. Sci. 89, 299 (1960).

    Article  Google Scholar 

  349. Schmidt, C. G., u. A. Bohne: DBP 944, 395.

    Google Scholar 

  350. 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).

    PubMed  CAS  Google Scholar 

  351. Schroeder, W., and H. A. Hoeksema: A new antibiotic, 6-amino-9-D-psicofuranine. J. Amer. chem. Soc. 81, 1767 (1959).

    Article  CAS  Google Scholar 

  352. Schulte, G.: Erfahrungen mit neuen cytostatischen Mitteln bei Hämoblastosen und Carcinomen und die Abgrenzung ihrer Wirkungen gegen Röntgentherapie. Z. Krebsforsch. 58, 500 1(952).

    Google Scholar 

  353. 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.

    Google Scholar 

  354. 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).

    Google Scholar 

  355. Schulte, G.: Weitere Erfahrungen mit Sanamycin bei der Behandlung der Lymphogranulomatose. Strahlentherapie 94, 491 (1954).

    PubMed  CAS  Google Scholar 

  356. Schulten, H., U. W. Pribilla: Tumorbehandlung mit cytostatischen Substanzen. Med. Klin. 50, 1631 (1955).

    CAS  Google Scholar 

  357. Schultze, H.: Kasuistischer und therapeutischer Beitrag zum Plasmozytom-Problem. Sammlung seltener klinischer Fälle. Heft 15, 97 Leipzig: Thieme 1958.

    Google Scholar 

  358. Schwenkenbecher, H., U. H. Hillger: Die kombinierte Behandlung der Lympho-granulomatose mit Röntgenstrahlen und Sanamycin. Med. Klin. 51, 263 (1956).

    CAS  Google Scholar 

  359. 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).

    Article  PubMed  CAS  Google Scholar 

  360. 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).

    CAS  Google Scholar 

  361. Shanbrom. E.: Advances in cancer chemotherapy. J. chron. Dis. 13, 69 (1961).

    Article  PubMed  Google Scholar 

  362. 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).

    Article  CAS  Google Scholar 

  363. Shima, T., H. Kanamori, T. Hoshi, C. Morita and T. Hata: Study on treatment with mitomycin against experimental malignancy. Chemotherap. 4, 304 (1956).

    Google Scholar 

  364. Shimada, N.: Clinical experiences with carzinophilin. Gann 47, 465 (1956).

    CAS  Google Scholar 

  365. 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).

    Article  Google Scholar 

  366. K. Kubota, K. Sukie, T. Noguchi and T. Takeishi: Experimental and clinical studies on mitomycins A and X. Chemotherap. 4, 305 (1956).

    Google Scholar 

  367. K. Kubota: Clinical experiments with carzinophilin. Nihon Ishikai Zasshi 33, 264 (1958).

    Google Scholar 

  368. 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).

    Google Scholar 

  369. Shiraha, Y.: Further observation on the clinical effectiveness of mitomycin C, an antitumor antibiotic. Antibiot. Ann. 1959—1960, 970.

    Google Scholar 

  370. 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.

    Google Scholar 

  371. 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.

    Google Scholar 

  372. Sivak, A., F. Nobili and E. Katz: Biogenesis of the chromopeptide actinomycin. Bact. Proc. 1960, 149.

    Google Scholar 

  373. Skipper, H. E., J. R. Thomson and M. Bell: Attempts at dual blocking of biochemical events in cancer chemotherapy. Cancer Res. 14, 503 (1954).

    PubMed  CAS  Google Scholar 

  374. Skipper, H. E., L. L. Bennett jr. and F. M. Schabel jr.: The mechanism of action of azaserine. Fed. Proc. 13, 298 (1954).

    Google Scholar 

  375. Skipper, H. E.: Annual Prog. Rep. on Cancer Chemoth. and mechanism of action of anticancer drugs. Southern Res. Inst. Birmingham, Alabama (1955).

    Google Scholar 

  376. Slechta, L.: Studies on the mode of action of psicofuranine. Biochem. Pharmacol. 5, 96 (1960).

    Article  PubMed  CAS  Google Scholar 

  377. 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).

    CAS  Google Scholar 

  378. Smith, C. G.: Tissue culture. Bioassay methods for Streptovitacin A. Proc. Soc. exp. Biol. (N. Y.) 100, 757 (1959).

    CAS  Google Scholar 

  379. 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).

    PubMed  CAS  Google Scholar 

  380. Smith, C. G.: Studies on the mode of action of streptovitacin A. Cancer Res. 20, 1394 (1960).

    CAS  Google Scholar 

  381. Smith, C. G.: An improved tissue culture assay. I. Methodology and cytotoxicity of anti-tumor agents. Cancer Res. 19, 843 (1959).

    CAS  Google Scholar 

  382. 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).

    CAS  Google Scholar 

  383. Sokoloff, B.: Progress in cancer chemotherapy: The oncolytic antibiotics. Progr. exp. Tumor Res. 1, 360 (1960).

    CAS  Google Scholar 

  384. Sokoloff, B., and B. Mc Connell: Host defence and chemotherapy in experimental cancer. 8. Internat. Krebscongress, Moskau 1962, S. 323.

    Google Scholar 

  385. Sokolski, W. T., N. J. Eilers and G. M. Savage: Antibiotics Ann. S. 551. Med. Encyclopedia N. Y. 1959.

    Google Scholar 

  386. 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).

    Google Scholar 

  387. 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).

    Article  CAS  Google Scholar 

  388. 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).

    PubMed  CAS  Google Scholar 

  389. 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).

    Google Scholar 

  390. Stock, C. C., A. Clarke, F. S. Philips and R. K. Barclay: Sarcoma 180 screening data. Cancer Res. 20, CS 1 (1960).

    Google Scholar 

  391. Sugawara, R., and T. Hata: Mitomycin, a new antibiotic from streptomyces. 2. Description of the strain. J. Antibiot. (Tokyo) Ser. A. 9, 147 (1956).

    Google Scholar 

  392. 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).

    CAS  Google Scholar 

  393. Sugiura, K., and H. J. Creech: Merits of ascites tumors for chemotherapeutic screening. Ann. N. Y. Acad. Sci. 63, 962 (1956).

    Article  PubMed  CAS  Google Scholar 

  394. 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).

    CAS  Google Scholar 

  395. Sugiura, K., C. C. Stock: The effect of mitomycin on a spectrum of tumors. Proc. Amer. Cancer Res. 2, 350 (1958).

    Google Scholar 

  396. Sugiura, K., C. C. Stock:Effect of compounds on the friend mouse virus leukemia. Proc. 7. Internat. Cancer Congress (London) 187 (1958).

    Google Scholar 

  397. 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).

    PubMed  CAS  Google Scholar 

  398. Sugiura, K.: The effect of actinomycin Dona spectrum of tumors. Ann. N. Y. Acad. Sci. 89, 368 (1960).

    Article  CAS  Google Scholar 

  399. Sugiura, K.: Experimental chemotherapy of cancer. — A report of progress. Progr. exp. Tumor Res. 2, 332 (1961).

    PubMed  CAS  Google Scholar 

  400. Sukie, K., T. Takeishi and T. Noguchi: Clinical application of mitomycin C. Chemothe- rap. 5, 223 (1957).

    Google Scholar 

  401. Tachibana, J.: Histopathological studies on autopsied cases of stomach cancer treated with anticancerous drugs. Tohoku J. exp. Med. 76, 279 (1961).

    CAS  Google Scholar 

  402. 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).

    Google Scholar 

  403. Takeishi, T.: Effect of carzinophilin on the bone marrow. Chemotherap. 4, 252 (1956).

    Google Scholar 

  404. Tal, M., and D. Elson: The reversible release of protein, ribonucleic acid and deoxy- ribonuclease from ribosomes. Biochim. biophys. Acta (Amst.) 53, 227 (1961).

    Article  CAS  Google Scholar 

  405. Talley, R. W., Y. L. Beckett and J. E. Kelley: Streptovitacin A: Clinical trial. Proc. Amer. Ass. Cancer Res. 3, 155 (1960).

    Google Scholar 

  406. Tan, C. T. C., H. W. Dargeon and J. H. Burchenal: The effect of actinomycin D on cancer in childhood. Pediatrics 24, 544 (1959).

    PubMed  CAS  Google Scholar 

  407. 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).

    Article  PubMed  CAS  Google Scholar 

  408. Tapie, J.: Résultats de l’emploi de l’actinomycine C en thérapeutique. Presse méd. 63, 1684 (1955).

    PubMed  CAS  Google Scholar 

  409. 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).

    Google Scholar 

  410. 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).

    PubMed  CAS  Google Scholar 

  411. 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).

    Google Scholar 

  412. Teranaka, T: Evaluation of antitumor activity of mitomycin. J. Antibiot. (Tokyo) Ser. A 10, 126 (1958).

    Google Scholar 

  413. Teller, H.: Zur Kasuistik der Retikulosarkomatosen. Derm. Wschr. 139, Heft 7. (1959)

    Google Scholar 

  414. 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).

    CAS  Google Scholar 

  415. Beeinflussung der sublichtmikroskopischen Struktur von Tumorzellen durch Cytostatika. Symposium über Krebsprobleme, S. 95, Düsseldorf 1960. Berlin-Göttingen- Heidelberg: Springer-Verlag 1961.

    Google Scholar 

  416. Thorne, C. B., C. G. Gomez and R. D. Housewright: Transamination of D-amino acids by bacillus subtilis. J. Bact. 69, 357 (1955).

    Article  PubMed  CAS  Google Scholar 

  417. Thorne, C. B., and D. M. Molnar: D-amino acid transamination in bacillus anthracis. J. Bact. 70, 420 (1955).

    PubMed  CAS  Google Scholar 

  418. 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).

    Google Scholar 

  419. 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).

    PubMed  CAS  Google Scholar 

  420. 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.

    Google Scholar 

  421. Trussel, P. C., and E. M. Richardson: Actinomycin from a new streptomyces. Canad. J. Res. 26, 27 (1948).

    Article  Google Scholar 

  422. 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).

    CAS  Google Scholar 

  423. Tuchmann-Duplessis, H., et L. Mercier-Parot: Apropos of the teratogenic action of actinomycin. C. R. Soc. Biol. (Paris) 153, 1697 (1959).

    Google Scholar 

  424. 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).

    Google Scholar 

  425. 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).

    Google Scholar 

  426. Tulinsky, A.: The structure of mitomycin A. J. A.Er. ehem. Soc. 84, 3188 (1962).

    Article  CAS  Google Scholar 

  427. Umezawa, H., S. Hayano, T. Takeuchi and Y. Mizuhara: Isolation of actinomycin A from a strain of streptomyces. J. Penicillin (Japan) 1, 129 (1947).

    CAS  Google Scholar 

  428. 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).

    CAS  Google Scholar 

  429. 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).

    Google Scholar 

  430. 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).

    Google Scholar 

  431. Usubuchi, I.: Effect of mitomycins on experimental tumors. Chemotherap. 5, 222 (1957).

    Google Scholar 

  432. 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).

    CAS  Google Scholar 

  433. Usubuchi, I., S. Oboshi, R. Tsuchida and H. Tanabe: Chemotherap. 6, 318 (1958).

    Google Scholar 

  434. Van Rymenant, M.: Production de methemoglobine par la mitomycine C in vivo et in vitro. 8. Internat. Krebscongress, Moskau 1962, S. 553.

    Google Scholar 

  435. Vogelsang, K. H., U. A. Tobben: Ein Beitrag zur Prognose und Therapie der Lympho- granulomatose. Strahlentherapie 101, Heft 1 (1956).

    Google Scholar 

  436. 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).

    Google Scholar 

  437. 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).

    CAS  Google Scholar 

  438. 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).

    CAS  Google Scholar 

  439. Waksman, S. A., and R. E. Curtis: The actinomyces of the soil. Soil Sci. 1, 99. (1916)

    Article  CAS  Google Scholar 

  440. 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).

    Article  CAS  Google Scholar 

  441. 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).

    CAS  Google Scholar 

  442. Waksman, S. A.: The soil as a source of microorganisms antagonistic to disease-producing bacteria. J. Bact. 40, 583 (1940).

    Google Scholar 

  443. Waksman, S. A.: Actinomyces antibioticus, a new soil organism antagonist to pathogenic and non-pathogenic bacteria. J. Bact. 42, 231 (1941).

    PubMed  CAS  Google Scholar 

  444. Waksman, S. A., and M. Tishler: The chemical nature of actinomycin, an antimicrobial substance produced by actinomyces antibioticus. J. biol. Chem. 142, 519 (1942).

    CAS  Google Scholar 

  445. Waksman, S. A., and E. Bugie: Action of antibiotic substances upon Ceratostomella ulmi. Proc. Soc. exp. Biol. (N. Y.) 54, 79 (1943).

    CAS  Google Scholar 

  446. 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).

    Article  CAS  Google Scholar 

  447. Waksman, S. A., E. Katz and L. C. Vining: Nomenclature of the actinomycins. Proc. Nat. Acad. Sci. (Wash.) 44, 602 (1958).

    Article  CAS  Google Scholar 

  448. 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).

    Article  PubMed  CAS  Google Scholar 

  449. Wallach, D. P., and R. C. Thomas: Psicofuranine VIII. Some pharmacological ob¬servations. Antibiot. and Chemother. 9, 722 (1959).

    CAS  Google Scholar 

  450. Warburg, O.: tJber den Stoffwechsel der Tumoren. Berlin 1926.

    Google Scholar 

  451. 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).

    Article  Google Scholar 

  452. Weissbach, H., and E. Katz: Studies on the biosynthesis of actinomycin: Enzymic synthesis of the phenoxazone chromophore. J. biol. Chem. 236, PC 16 (1961).

    Google Scholar 

  453. Welch, A. D.: The problem of drug resistance in cancer chemotherapy. Cancer Res. 19, 359 (1959).

    PubMed  CAS  Google Scholar 

  454. 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).

    CAS  Google Scholar 

  455. Werkheiser, W. C.: Specific binding of 4-amino folic acid analogues by folic acid reductase. J. biol. Chem. 286, 888 (1961).

    Google Scholar 

  456. Whitelocks, O. ST. V.: Genetic concept for the origin of cancer. Ann. N. Y. Acad. Sci. 71, art. 6, 807–1241 (1958).

    Google Scholar 

  457. Wilmanns, W.: Zum Wirkungsmechanismus von 6-mercaptopurin. Klin. Wschr. 40, 1170 (1962).

    Article  PubMed  CAS  Google Scholar 

  458. Wissemann, C. L. jr., F. E. Hahn, H. Hopps and J. E. Smadel: Chloramphenicol inhibition of protein synthesis. Fed. Proc. 12, 466 (1953).

    Google Scholar 

  459. Woodruff, H. B., and S. A. Waksman: Historical Background. Ann. N. Y. Acad. Sci. 89, 287 (1960).

    Article  PubMed  CAS  Google Scholar 

  460. 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).

    Article  CAS  Google Scholar 

  461. Yamamoto, T., S. Yamaoko, H. Umezawa, T. Takeuchi and K. Nitta: Antitumor effects of sarkomycin. Gann 45, 503 (1954).

    Google Scholar 

  462. 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).

    Article  Google Scholar 

  463. Zakrzewski, S. F., and C. A. Nichol: Evidence for a single enzyme reducing folate and dihydrofolate. J. biol. Chem. 235, 2984 (1961).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 1963 Springer-Verlag OHG. Berlin · Göttingen · Heidelberg

About this paper

Cite this paper

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

Download citation

  • DOI: https://doi.org/10.1007/978-3-642-94862-6_8

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-94863-3

  • Online ISBN: 978-3-642-94862-6

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics