In vitro cytotoxicity patterns of standard and investigational agents on human bone marrow granulocyte-macrophage progenitor cells
| Autor: | B. Tomasovic, Benjamin Drewinko, K. Dicke, Jaffer A. Ajani, V. M. Hug, G. Spitzer |
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| Jazyk: | angličtina |
| Rok vydání: | 1986 |
| Předmět: |
Drug
Cancer Research Cell Survival media_common.quotation_subject Microgram Dacarbazine Drug Evaluation Preclinical Antineoplastic Agents Pharmacology Biology Procarbazine In vivo medicine Humans Cytotoxicity Biotransformation Cells Cultured media_common Ifosfamide Dose-Response Relationship Drug Macrophages Hematopoietic Stem Cells In vitro Oncology medicine.drug Research Article Granulocytes |
| Zdroj: | British Journal of Cancer |
| ISSN: | 1532-1827 0007-0920 |
| Popis: | Inhibitory concentrations (ICs) against human bone marrow granulocyte-macrophage colony forming cells (GM-CFC) were established for 26 cancer chemotherapy agents, including seven investigational agents by ten day exposure. Each drug was tested at four or more concentrations to generate reliable survival curves. The analysis of the survival curves produced three patterns according to which drugs were classified: class A drugs had a shouldered curve with terminal exponential kill of GM-CFC, class B drugs produced initial exponential component followed by a plateau, and class C drugs produced linear curves. These categories provide the relationship between drug concentration and cytotoxicity, e.g., the cytotoxicity of class B drugs, after initial kill, did not increase in spite of serial doubling of concentrations whereas the class C drugs had proportional killing with two-fold concentration increment. A number of drugs were active at in vitro concentrations of less than or equal to 0.01 microgram ml-1 and caused log reduction of GM-CFC with an approximate concentration of 0.0001 microgram ml-1. Drugs known to require in vivo bioactivation, namely dacarbazine, procarbazine, and ifosfamide were active at high concentrations (greater than 10.0 micrograms ml-1). We propose that for myelosuppressive agents the GM-CFC provides a useful biologic reference to determine in vitro cut off concentrations to be utilized for drug screening. For nonmyelosuppressive agents, however, it may be suboptimal. |
| Databáze: | OpenAIRE |
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