Evidence for characteristic vascular patterns in solid tumours: quantitative studies using corrosion casts.

The vascular architecture of four different tumour cell lines (CaX, CaNT, SaS, HEC-1B) transplanted subcutaneously in mice was examined by means of microvascular corrosion casting in order to determine whether there is a characteristic vascular pattern for different tumour types and whether it differs significantly from two normal tissues, muscle and gut. Three-dimensional reconstructed scanning electron microscope images were used for quantitative measurements. Vessel diameters, intervessel and interbranch distances showed large differences between tumour types, whereas the branching angles were similar. In all tumours, the variability of the vessel diameters was significantly higher than in normal tissue. The quantitative data provide strong evidence for a characteristic vascular network determined by the tumour cells themselves.

Vascular patterns of tumors: scanning and transmission electron microscopic studies on human xenografts.

The tumor vascular system plays a significant role both in tumor growth and metastasis as well as in therapy. However, there are comparatively few papers dealing with the morphology and architecture of tumor vascularity. This is inconceivable insofar as structural and architectural parameters determine tumor blood flow. Therefore, the vascular system of eight human tumor lines transplanted onto 121 thymus-aplastic nude mice was studied with light, scanning and transmission electron microscopy as well as microvascular corrosion casting. All tumors show a connective tissue-like capsule with a dense plexus of vessels forming a "vascular envelope". Particularly in early stages, these vessels follow a tortuous course with glomeruloidal arrangement and numerous indications of angiogenic activity. In the tumor centre regular arteries and veins are never to be seen. Instead, all vessels show a capillary wall construction with variations in height and electron densities of the endothelial cells. Changes in vessel diameter, lack of vascular hierarchy, blind ends as well as irregular sinusoidal systems originating from and draining to veins are common features. The vascular densities vary considerably within single tumors. Based on the vascular architecture and wall construction, necroses may occur even in areas with intervascular distances of only 15 microns. No significant differences in vascular architecture of the various cell lines could be observed.