MedicineBiology

J. Denekamp

1993.3.1BRITISH JOURNAL OF RADIOLOGY

DOI: 10.1259/0007-1285-66-783-181

tlooto Summary

A body of evidence that vascular-mediated damage occurs in murine tumours after many existing forms of anti-tumour therapy is rapidly accumulating means that a change in the approach to experimental cancer therapy is needed to ensure that this important new avenue is fully investigated.

Abstract

A body of evidence that vascular-mediated damage occurs in murine tumours after many existing forms of anti-tumour therapy is rapidly accumulating (see Gray Conference Proceedings edited by Moore & West, 1991). Rapid conventional screens of cells in vitro or using leukaemias of lymphomas will not detect this mode of action and such screens will therefore miss effective agents. A change in the approach to experimental cancer therapy is needed to ensure that this important new avenue is fully investigated. Solid tumours will need to be studied and the importance of specific tumour cell biochemistry (e.g. on tissue factor procoagulant activity), of endothelial status and the immunocompetence of the host are all likely to be important. It is a subject of considerable debate at present whether transplanted subcutaneous mouse tumours are adequate models and whether they will reflect the response of spontaneous tumours, or even of transplants into other sites. Xenografts are not likely to be appropriate if the i...

Citation format

DENEKAMP, J. Angiogenesis, neovascular proliferation and vascular pathophysiology as targets for cancer therapy. BRITISH JOURNAL OF RADIOLOGY, 1993, 66: 181–196.