TY - JOUR
T1 - In vitro cytotoxicity patterns of standard and investigational agents on human bone marrow granulocyte-macrophage progenitor cells
AU - Ajani, J. A.
AU - Spitzer, G.
AU - Tomasovic, B.
AU - Drewinko, B.
AU - Hug, V. M.
AU - Dicke, K.
N1 - Funding Information:
G. Spitzer, is a recipient of a scholarship from the Leukemia Society of America.
PY - 1986/10
Y1 - 1986/10
N2 - 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 increments. A number of drugs were active at in vitro concentrations of ≤ 0.01 μg ml–1 and caused log reduction of GM-CFC with an approximate concentration of 0.001 μg ml–1. Drugs known to require in vivo bioactivation, namely dacarbazine, procarbazine, and ifosfamide were active at high concentrations (>10.0 μg 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.
AB - 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 increments. A number of drugs were active at in vitro concentrations of ≤ 0.01 μg ml–1 and caused log reduction of GM-CFC with an approximate concentration of 0.001 μg ml–1. Drugs known to require in vivo bioactivation, namely dacarbazine, procarbazine, and ifosfamide were active at high concentrations (>10.0 μg 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.
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U2 - 10.1038/bjc.1986.216
DO - 10.1038/bjc.1986.216
M3 - Article
C2 - 3778805
AN - SCOPUS:0022974398
SN - 0007-0920
VL - 54
SP - 607
EP - 613
JO - British journal of cancer
JF - British journal of cancer
IS - 4
ER -