Skip to main content
British Journal of Cancer logoLink to British Journal of Cancer
. 1982 Oct;46(4):557–567. doi: 10.1038/bjc.1982.240

Vascular structure of five human malignant melanomas grown in athymic nude mice.

O V Solesvik, E K Rofstad, T Brustad
PMCID: PMC2011199  PMID: 7138764

Abstract

The vascular structure of 5 human malignant melanomas grown in athymic nude mice was characterized. The vessels were filled with a radio-opaque medium administered via the abdominal aorta of the mice. X-ray images, obtained from 720 micrometers-thick tumour sections, provided qualitative information on the vascular structure of the tumours. Histograms for vessel length, surface, and volume as a function of vessel diameter were obtained by stereological analysis of 2 micrometers-thick sections. The volume fraction of necrotic tissue in the tumours was also determined by stereological analysis. The 5 melanomas exhibited individual, characteristic vascular structures as well as individual, characteristic necrotic fractions. The total vessel length ranged from 32 +/- 2 to 80 +/- 4 mm, the total vessel surface from 1.6 +/- 0.1 to 3.8 +/- 0.2 mm2, and the total vessel volume from 0.009 +/- 0.001 to 0.022 +/- 0.002 mm3--all values per mm3 histologically intact tumour tissue. The necrotic fractions ranged from 30 +/- 1 to 49 +/- 4%, and tended to be higher in the poorly than in the well-vascularized melanomas. The volume doubling times ranged from 4.2 to 21.6 days. Melanomas with short volume-doubling times had lower necrotic fractions and tended to be better vascularized than those with long volume-doubling times.

Full text

PDF
557

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Falk P. Patterns of vasculature in two pairs of related fibrosarcomas in the rat and their relation to tumour responses to single large doses of radiation. Eur J Cancer. 1978 Mar;14(3):237–250. doi: 10.1016/0014-2964(78)90187-1. [DOI] [PubMed] [Google Scholar]
  2. Field S. B., Bleehen N. M. Hyperthermia in the treatment of cancer. Cancer Treat Rev. 1979 Jun;6(2):63–94. doi: 10.1016/s0305-7372(79)80043-2. [DOI] [PubMed] [Google Scholar]
  3. Folkman J. The vascularization of tumors. Sci Am. 1976 May;234(5):58-64, 70-3. doi: 10.1038/scientificamerican0576-58. [DOI] [PubMed] [Google Scholar]
  4. Hilmas D. E., Gillette E. L. Microvasculature of C3H/Bi mouse mammary tumors after x-irradiation. Radiat Res. 1975 Jan;61(1):128–143. [PubMed] [Google Scholar]
  5. Jørgen H., Gundersen G. Estimation of tubule or cylinder LV, SV and VV on thick sections. J Microsc. 1979 Dec;117(3):333–345. doi: 10.1111/j.1365-2818.1979.tb04690.x. [DOI] [PubMed] [Google Scholar]
  6. Kennedy K. A., Teicher B. A., Rockwell S., Sartorelli A. C. The hypoxic tumor cell: a target for selective cancer chemotherapy. Biochem Pharmacol. 1980 Jan 1;29(1):1–8. doi: 10.1016/0006-2952(80)90235-x. [DOI] [PubMed] [Google Scholar]
  7. POWERS W. E., TOLMACH L. J. A multicomponent x-ray survival curve for mouse lymphosarcoma cells irradiated in vivo. Nature. 1963 Feb 16;197:710–711. doi: 10.1038/197710b0. [DOI] [PubMed] [Google Scholar]
  8. Rofstad E. K., Brustad T. Radiation response in vitro of cells from five human malignant melanoma xenografts. Int J Radiat Biol Relat Stud Phys Chem Med. 1981 Dec;40(6):677–680. doi: 10.1080/09553008114551671. [DOI] [PubMed] [Google Scholar]
  9. Song C. W., Kang M. S., Rhee J. G., Levitt S. H. Vascular damage and delayed cell death in tumours after hyperthermia. Br J Cancer. 1980 Feb;41(2):309–312. doi: 10.1038/bjc.1980.45. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Steel G. G., Peckham M. J. Human tumour xenografts: a critical appraisal. Br J Cancer Suppl. 1980 Apr;4:133–141. [PMC free article] [PubMed] [Google Scholar]
  11. Steel G. G. The growth and therapeutic response of human tumours in immune deficient mice. Bull Cancer. 1978;65(4):465–472. [PubMed] [Google Scholar]
  12. THOMLINSON R. H., GRAY L. H. The histological structure of some human lung cancers and the possible implications for radiotherapy. Br J Cancer. 1955 Dec;9(4):539–549. doi: 10.1038/bjc.1955.55. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Tannock I. F. Oxygen diffusion and the distribution of cellular radiosensitivity in tumours. Br J Radiol. 1972 Jul;45(535):515–524. doi: 10.1259/0007-1285-45-535-515. [DOI] [PubMed] [Google Scholar]
  14. VOGEL A. W. INTRATUMORAL VASCULAR CHANGES WITH INCREASED SIZE OF A MAMMARY ADENOCARCINOMA: NEW METHOD AND RESULTS. J Natl Cancer Inst. 1965 May;34:571–578. [PubMed] [Google Scholar]
  15. Yamaura H., Matsuzawa T. Tumor regrowth after irradiation; an experimental approach. Int J Radiat Biol Relat Stud Phys Chem Med. 1979 Mar;35(3):201–219. doi: 10.1080/09553007914550241. [DOI] [PubMed] [Google Scholar]

Articles from British Journal of Cancer are provided here courtesy of Cancer Research UK

RESOURCES