Skip to main content
Log in

Das Hamstermelanom M Mel 1 als Ascitestumor

II. Untersuchungen über die Behandlungsmöglichkeiten beim Ascitesmelanom Vergleich mit den Therapiemöglichkeiten bei anderen Melanomen

The hamster melanoma M Mel 1 as ascites tumor

II. Research concerning the therapeutic possibilities with this ascites melanoma comparison with therapeutic effects in other melanomas

  • Published:
Archiv für klinische und experimentelle Dermatologie Aims and scope Submit manuscript

Summary

X-ray treatment of the spontaneous malignant melanomas of mice has been investigated thoroughly. The S 91 melanoma is relatively sensitive to irradiation, whereas ionizing radiation has practically no effect on Harding-Passey melanoma.

Our observations of ascites melanoma have shown that after inoculation of 107 tumor cells, irradiation with 6000 r/150 KV/0.5 Cu cause no change in the rate of the takes. The radiation effect on the melanoma cells can only be judged by a prolongation of the survival time.

In contrast to the reduced sensitivity to ionizing radiation, the ascites melanoma is very sensitive to l-phenylalanin-mustard (Alkeran). Even with the same number of tumor cells as in the radiation experiments, nearly all animals can be healed. Other substances showed very little effect.

The Harding-Passey melanoma has been best studied as regards chemotherapy, it shows only a limited chemosensitivity, this being somewhat better in S 91 melanoma.

The results of research done by various authors and ourselves have shown that the immunotherapeutic possibilities are still very limited. Only the use of exact methods occasionally reveals a slight degree of immunization.

Zusammenfassung

Die Strahlenbehandlung der spontanen malignen Mäusemelanomen ist sehr eingehend untersucht worden. Das Melanom S 91 ist relativ strahlenempfindlich; demgegenüber ist das Harding-Passey-Melanom weitgehend strahlenresistent.

Unsere Untersuchungen am Ascites-Melanom (Asc-M Mel 1) des Goldhamsters haben gezeigt, daß bei der Verwendung von 107 Tumorzellen 6000 r/180 KV/0,5 Cu keine Veränderung der Angehrate verursachen. Der gesetzte Strahlenschaden läßt sich nur in einer Verlängerung der Überlebensdauer abschätzen.

Im Gegensatz zur reduzierten Strahlenempfindlichkeit ist das Ascites-Melanom gegenüber dem alkylierenden Stoff Alkeran sehr sensibel. Auch bei gleicher Tumorzellzahl wie in den Strahlenversuchen sind praktisch alle Tiere heilbar. Andere Substanzen hingegen sind wenig wirksam.

Das Harding-Passey-Melanom ist in bezug auf die Chemotherapie weitgehend am besten untersucht; es zeigt nur eine sehr geringfügige Chemosensibilität. Diese ist beim S 91-Melanom etwas besser.

Untersuchungen von verschiedenen Autoren und uns selbst haben gezeigt, daß die immuno-therapeutischen Möglichkeiten noch sehr klein sind. Nur bei Verwendung exakter Methoden läßt sich gelegentlich eine leichte Immunisierung nachweisen.

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

Access this article

Subscribe and save

Springer+ Basic
$34.99 /Month
  • Get 10 units per month
  • Download Article/Chapter or eBook
  • 1 Unit = 1 Article or 1 Chapter
  • Cancel anytime
Subscribe now

Buy Now

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Literatur

  • Ariel, I. M., G. T. Pack, and D. Galey: Distribution of 131I iodoquin in animals with melanoma. Proc. Amer. Ass. Cancer Res. 8, 3 (1967).

    Google Scholar 

  • Bashkaev, I. S., and G. I. Rozenbaum: Transplantable Harding-Passey melanoma studied by the gelprecipitation reaction. Vop. Onkol. 9, 83 (1963).

    Google Scholar 

  • Blois, M. S., and R. F. Kallman: The incorporation of 14C from 3,4-dihydroxyphenylalanine-2′-C14 into the melanin of mouse melanomas. Cancer Res. 24, 863–868 (1964).

    Google Scholar 

  • Conn, J. H., and W. R. Fain: Immunological studies with hamster melanoma. Surg. Forum 10, 1–3 (1960).

    Google Scholar 

  • Crile, G., Jr.: Heat as an adjunct to the treatment of cancer. Cleveland Clin. Quart. 28, 75–89 (1961).

    Google Scholar 

  • Demopoulos, H. B.: Effects of low phenylalanine-tyrosine diets on S-91 mouse melanomas. J. nat. Cancer Inst. 37, 185–190 (1966).

    Google Scholar 

  • —, and G. Kaley: Selective inhibition of respiration of pigmented S-91 mouse melanomas by phenyl lactase, and the possibly related effects on growth. J. nat. Cancer Inst. 30, 611–633 (1963).

    Google Scholar 

  • Flatow, H. H.: Untersuchungen zur Strahlenempfindlichkeit des Harding-Passey-Melanoms der Maus. Dissertation, Hamburg 1964.

  • Hempel, K., u. M. Deimel: Untersuchungen zur gezielten Strahlentherapie des Melanoms und des chromaffinen Systems durch selektive H-3-Inkorporation nach Gabe von H-3-markiertem DOPA. Strahlentherapie 121, 22–45 (1963).

    Google Scholar 

  • Hoye, R. C., and R. R. Smith: The effectiveness of small amounts of preoperative irradiation in preventing the growth of tumor cells disseminated at surgery. Cancer 14, 284–295 (1961).

    Google Scholar 

  • —, G. H. Weiss, and A. S. Ketcham: Growth rate of experimental tumor after the use of Laser energy. J. nat. Cancer Inst. 37, 819–823 (1967).

    Google Scholar 

  • Kramer, W. M., R. V. Eck, and R. R. Smith: Prevention of experimental lung metastases with triethylenethiophosphoramide (ThioTEPA). Surg. Gynec. Obstet. 106, 427–434 (1958).

    Google Scholar 

  • Li, M. C.: Enhancement of drug cure-rate of cancer by hetero-tumor immunization. Proc. Amer. Ass. Cancer Res. 7, 165, (1966).

    Google Scholar 

  • Luck, J. M.: The action of the phenylalanine mustards and of several homologs on mouse melanoma. Cancer Res. 17, 1071–1076 (1957).

    Google Scholar 

  • Olch, P. D., P. V. Eck, and R. R. Smith: An experimental study of the effect of external irradiation on a “Primary” tumor and its distant metastases. Cancer 12, 23–26 (1959).

    Google Scholar 

  • ———: An experimental study on the effect of irradiation on the dissemination of cancer. Cancer Res. 19, 464–467 (1959).

    Google Scholar 

  • Ott, F., and H. Storck: Investigations on the effect of sodium cyclohexanolsuccinate on the hamster melanoma A Mel 3. Progr. biochem. Pharmacol. 1, 327–330 (1959).

    Google Scholar 

  • Riley, V.: The melanoma as a model in a rational chemotherapy study. Pigment cell biology (Gordon), pp. 389–433. New York: Academic Press Inc. 1959.

    Google Scholar 

  • Rohde, B., u. A. Wiskemann: Über das Wachstum röntgenbestrahlter Melanomalignome in der Gewebekultur und im Transplantationsversuch. Strahlentherapie 123, 534–544 (1964).

    Google Scholar 

  • Rosenberg, S. A.: In vivo and in vitro demonstration of tumor immunity to the transplanted melanoma of hamsters. Bull. Johns Hopk. Hosp. 108, 386–387 (1961).

    Google Scholar 

  • Salamon, T., u. H. Storck: Über die Sensibilität des Hamstermelanoms gegenüber Röntgenstrahlen, Kälte, Cytostatica und immunobiologischen Einflüssen. Arch. klin. exp. Derm. 216, 161–185 (1963).

    Google Scholar 

  • Schabel, F. M., Jr., 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. (Suppl.) 1961, 235–342.

  • Scolari, E., D. Boiti, M. Nannelli e C. Vallecchi: Prime ricerche sperimentali e osservazioni cliniche sull'impiego di un nuovo radiosensibilizzante nella radiotherapia dei tumori. Rass. Derm. Sif. 12, 207–218 (1959).

    Google Scholar 

  • Sugiura, K.: The effect of various factors on the Hardin-Passey melanoma of the mouse. Cancer Res. 4, 282–288 (1944).

    Google Scholar 

  • —: The effects of various physical and chemical factors on transplantable mouse melanoma. The biology of melanoma, p. 369. New York: Spec. Publ. N.Y. Acad. Sci. 1948.

    Google Scholar 

  • —: Studies on 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).

    Google Scholar 

  • —: Chemotherapy of Harding-Passey melanoma. Ann. N. Y. Acad. Sci. 100, 334–347 (1963).

    Google Scholar 

  • Vedrich, M., M. O. Greene, and J. Greenberg: Cloudman mouse melanoma S-91, as a potential screening tool in cancer chemotherapy. Cancer Res. 21, 359–376 (1961).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Ott, F. Das Hamstermelanom M Mel 1 als Ascitestumor. Arch. klin. exp. Derm. 234, 384–398 (1969). https://doi.org/10.1007/BF00508335

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00508335

Navigation