Abstract

AbstractWe isolated three dimensional cell clusters from fresh human solid tumors and also isolated human neoplastic and normal lymphatic cells. Cells were cultured for 96 hours with and without bevacizumab and other agents. At concentrations of bevacizumab which completely removed VEGF from the culture medium, dead microvascular cells were detected through Fast Green/H&E staining as previously described. These peculiar staining characteristics suggested the involvement of calcium, and this was confirmed through staining with Alizarin red S. Using Alizarin staining as a marker for endothelial cell death permitted the use of public domain image analysis software which resulted in a sensitive and specific system for identifying active pharmaceuticals which target the tumor microvasculature at the same time direct antitumor cell effects are determined. Our results suggest an important role for calcium in endothelial cell death mediated by bevacizumab and other agents and further suggest that agents promoting calcium influx may potentiate the activity of antiangiogenic agents.

Highlights

  • The chief goal of cancer therapeutics has been the discovery of exploitable differences between cancer and normal cells, to allow for selective toxicity

  • We previously described a novel method for detecting endothelial cell death in primary cell cultures prepared from fresh biopsy specimens of human tumors and from peripheral blood[6]

  • We report here that the distinctive cytological staining of dead endothelial cells observed in our method is the result of calcium accumulation and that staining for calcium affords a sensitive method for detecting endothelial cell death in vitro

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Summary

Introduction

The chief goal of cancer therapeutics has been the discovery of exploitable differences between cancer and normal cells, to allow for selective toxicity. We previously described a novel method for detecting endothelial cell death in primary cell cultures prepared from fresh biopsy specimens of human tumors and from peripheral blood[6].

Results
Conclusion
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