Abstract

Clinically relevant concentrations of verapamil do not enhance the sensitivity of human bone marrow CFU-GM to adriamycin and VP16

Highlights

  • Bone marrow toxicity is a major dose-limiting factor in the clinical use of adriamycin and VP16 (VP16-213, etoposide)

  • We have studied the effect of verapamil at a range of concentrations on the sensitivity of human bone marrow granulocyte-macrophage stem cells (CFU-GM) to adriamycin and VP16

  • Lymphocyte conditioned medium was produced by light density peripheral blood mononuclear cells (PBNCs) from normal subjects obtained using Ficoll-diatrizoate separation

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Summary

Introduction

Bone marrow toxicity is a major dose-limiting factor in the clinical use of adriamycin (doxorubicin) and VP16 (VP16-213, etoposide). We have studied the effect of verapamil at a range of concentrations (including concentrations achievable in vivo) on the sensitivity of human bone marrow granulocyte-macrophage stem cells (CFU-GM) to adriamycin and VP16. In preliminary studies (subjects 5 and 6) colony number was determined in the presence and absence of the solvent used to dissolve the VP16 (i.e. 0.025% ethanol, final concentration).

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