Skip to main content
Journal of Cancer Research and Clinical Oncology logoLink to Journal of Cancer Research and Clinical Oncology
editorial
. 1982 Jul;103(3):211–226. doi: 10.1007/BF00409698

Vascularization of tumors: A review

Philippe Shubik 1,2
PMCID: PMC12252721  PMID: 6181069

Conclusion

It is apparent that tumors excite a vascular response that is generally greater than that seen with various other inciting factors. Epidermis appears to be capable of similar activity, whereas dermis does not. All the evidence so far obtained points to the presence of a diffusible factor inciting this reaction. It is now known that capillary budding in inflammatory and healing tissues is a accompanied by mitotic activity in endothelial cells and it would appear only logical to believe that a similar activity must accompany vascularization of tumors which indeed has been demonstrated to be the case. However, vascularization is a complex phenomenon and requires not only mitotic stimulation but various other changes that are not all defined. In spite of considerable work to quantify the vascular responses seen under various conditions, one must conclude objectively that none of the methods in current use are entirely satisfactory. In addition, the variations in methods employed, ranging from the use of the chick chorioallantoic membrane to the hamster cheek pouch, introduce many variables into this already complicated picture. Attempts to identify the specific chemical factor(s) responsible for the vascularization of tumors and/or other tissues have involved considerable efforts but have not so far succeeded in identifying a specific chemical. Questions of specificity, of quantitative rather than qualitative differences between tumors and other tissues, still remain. However, it is unquestionable that it is logical to attempt to identify the factor(s) involved and that this area of investigation provides one of the few straightforward approaches to the study of tumor therapy. Inhibition of tumor angiogenic factors appears to be a real possibility and should be continued. There would appear to be little doubt that there is considerable variation between different tumors in the stroma and vascular responses that they induce. Particularly striking is the fact that certain tumors can receive their blood supply via channels composed of tumor cells rather than through blood vessels lined with endothelium. This finding could certainly explain differences in radiosensitivity. It is most important that a variety of different tumors be examined for their vascular and stromal responses and that our present knowledge be enlarged to cover many other tumors. This entire field of activity is dependent upon technological advances. The three methods described for the study of vascularization—the hamster cheek-pouch chamber, the chorioallantoic membrane, and the cornea—are all considerable advances over past methods but none can be said to be free from undesirable complications nor amenable to adequate quantification. It is most important that new methods for the study of this phenomenon be sought. It is surprising not that some discrepant results have occurred, but rather that there are not many more.

Footnotes

The “Journal of Cancer Research and Clinical Oncology” publishes in loose succession “Editorials” and “Guest Editorials” on current and/or controversial problems in experimental and clinical oncology. These contributions represent exclusively the personal opinion of the author. The Editors Die Zeitschrift “Journal of Cancer Research and Clinical Oncology” bringt in zwangloser Folge “Editorials” und “Guest Editorials” zu aktuellen und/oder kontroversen Problemen der experimentellen und klinischen Onkologie. Diese Beiträge geben ausschließlich die persönliche Meinung des Autors wieder.

References

  1. Algire GH (1943) A adaptation of the transparent chamber technique to the mouse. J Natl Cancer Inst 4:1–11 [Google Scholar]
  2. Algire GH, Chalkley HW (1945) Vascular reactions of normal and malignant tissues in vivo. I. Vascular reactions of mice to wounds and to normal and neoplastic transplants. J Natl Cancer Inst 6:73–85 [Google Scholar]
  3. Auerbach R, Kubai L, Sidky J (1976) Angiogenesis induction by tumors, embryonic tissues and lymphocytes. Cancer Res 36:3425–3440 [PubMed] [Google Scholar]
  4. Brem W, Folkman J (1975) Inhibition of tumor angiogenesis mediated by cartilage. J Exp Med 141:427–439 [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Chalkley WH (1948) Comments on Algiri GH and Legallais FY. Growth and vascularization of transplantable mouse melanomas. Special publications of the NY Acad Sci 4:164 [Google Scholar]
  6. Clark ER, Kirby-Smith HT, Rex, RO, Williams RG (1930) Recent modifications in the method of studying living cells and tissues in transparent chambers inserted in the rabbit's ear. Anat Rec 47:187–211 [Google Scholar]
  7. Cliff WJ (1963) Observations on healing tissue: a combined light and electron microscopic investigation. Philos Trans R Soc Lond [Biol] 246:305–325 [Google Scholar]
  8. Donahue S (1964) A relationship between fine structure and function of blood vessels in the central nervous system of rabbit fetuses. Am J Anat 115:17–26 [DOI] [PubMed] [Google Scholar]
  9. Donahue S, Pappas GD (1961) The fine structure of capillaries in the cerebral cortex of the rat at various stages of development. Am J Anat 108:331 [DOI] [PubMed] [Google Scholar]
  10. Ehrmann RL, Knoth M (1968) Choriocarcinoma: transfilter stimulation of vasoproliferation in the hamster cheek pouch, studied by light and electromicroscopy. J Natl Cancer Inst 41:1329–1331 [PubMed] [Google Scholar]
  11. Folkman J, Merler E, Abernathy C, Williams G (1971) Isolation of a tumor factor responsible for angiogenesis. J Exp Med 133:275–288 [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Folkman J (1974) Tumor angiogenesis factor. Cancer Res 34:2109–2113 [PubMed] [Google Scholar]
  13. Goodall CM, Sanders AG, Shubik P (1965) Studies of vascular patterns in living tumors with a transparent chamber inserted in the hamster cheek pouch. J Natl Cancer Inst 35:497–521 [DOI] [PubMed] [Google Scholar]
  14. Greenblatt M, Shubik P (1968) Tumor angiogenesis: transfilter diffusion studies in the hamster by the transparent chamber technique. J Natl Cancer Inst 41:111–116 [PubMed] [Google Scholar]
  15. Grobstein C (1957) Some transmission characteristics of the tubule inducing influence on mouse metanephrogenic mesenchyme. Exp Cell Res 13:575–587 [DOI] [PubMed] [Google Scholar]
  16. Gullino P, Grantham FH (1964) The vascular space of growing tumors. Cancer Res 24:1727–1732 [PubMed] [Google Scholar]
  17. Hogan MJ, Feeney L (1963) The ultrastructure of the retinal blood vessels. I. Large vessels. II. The small vessels. J Ultrastruct Res 9:10–45 [DOI] [PubMed] [Google Scholar]
  18. Karrer HE (1960) Electron microscope study of developing chick embryo aorta. J Ultrastruct Res 4:420–454 [DOI] [PubMed] [Google Scholar]
  19. Karrer HE (1961) An electron microscope study of the aorta in young and in ageing mice. J Ultrastruct Res 5:1–27 [DOI] [PubMed] [Google Scholar]
  20. Langer R, Brem H, Falterman K, Klein M, Folkman J (1976) Isolation of a cartilage factor that inhibits tumor neovascularization. Science 193:70–72 [DOI] [PubMed] [Google Scholar]
  21. Leighton J (1967) The spread of cancer explored in the embryonated egg. In: The spread of cancer. Academic Press, New York pp 115–192 [Google Scholar]
  22. Nishioka K, Ryan TJ (1972) The influence of the epidermis and other tissues on blood vessel growth in the hamster cheek pouch. J Invest Derm 58:33–45 [DOI] [PubMed] [Google Scholar]
  23. Nishioka K, Katayama I (1978) Angiogenic activity in culture supernatant of antigen-stimulated lymph node cells. J Pathol 126:63–69 [DOI] [PubMed] [Google Scholar]
  24. Pugatch EMJ (1964) The growth of endothelium and pseudoendothelium on the healing surface of rabbit ear chambers. Proc R Soc Lond [Biol] 160:412–422 [DOI] [PubMed] [Google Scholar]
  25. Rijhsinghani K, Greenblatt M, Shubik P (1968) Vascular abnormalities induced by benzo(a)pyrene: an in vivo study in the hamster cheek pouch. J Natl Cancer Inst 41:205–209 [PubMed] [Google Scholar]
  26. Sanders AG, Shubik P (1964) A transparent window for use in the Syrian hamster. Israel J Exp Med 11:118 [Google Scholar]
  27. Sandison JC (1924) A new method for microscopic study of living growing tissues by the introduction of transparent chamber in the rabbit's ear. Anat Rec 28:281–287 [Google Scholar]
  28. Schoefl GI (1963) Studies on inflammation. III. Growing capillaries: Their structure and permeability. Virchows Arch [Pathol Anat] 337:97–141 [PubMed] [Google Scholar]
  29. Shubik P, Feldman R, Garcia H, Warren BA (1976) Vascularization induced in the cheek pouch of the Syrian hamster by tumor and nontumor substances. J Natl Cancer Inst 57:769–774 [DOI] [PubMed] [Google Scholar]
  30. Warren BA, Shubik P (1966) The growth of the blood supply to melanoma transplants in the hamster cheek pouch. Lab Invest 15:464–478 [PubMed] [Google Scholar]
  31. Warren BA (1965) Fibrinolytic properties and electron microscopic features of rabbit ear chamber endothelium. Br J Exp Pathol 46:607–614 [PMC free article] [PubMed] [Google Scholar]
  32. Warren BA (1966) The ultrastructure of capillary sprouts induced by melynoma transplants in hamsters. J R Microscop Soc 86:177–187 [DOI] [PubMed] [Google Scholar]
  33. Wood S Jr (1958) Pathogenesis of metastasis formation observed in the rabbit ear chamber. Arch Pathol 66:550–568 [PubMed] [Google Scholar]
  34. Wolf JE, Harrison RG (1973) Demonstration and characterization of an epidermal angiogenic factor. J Invest Derm 61:130–141 [DOI] [PubMed] [Google Scholar]

Articles from Journal of Cancer Research and Clinical Oncology are provided here courtesy of Springer

RESOURCES