Amifostine differentially modulates DNA damage evoked by idarubicin in normal and leukemic cells

被引:19
作者
Blasiak, J
Gloc, E
Mlynarski, W
Drzewoski, J
Skórski, T
机构
[1] Med Univ Lodz, Inst Pediat, Oncohaematol Unit, PL-91738 Lodz, Poland
[2] Med Univ Lodz, Dept Clin Pharmacol, PL-94214 Lodz, Poland
[3] Temple Univ, Coll Sci & Technol, Philadelphia, PA 19122 USA
[4] Univ Lodz, Dept Mol Genet, PL-90237 Lodz, Poland
关键词
amifostine; idarubicin; DNA damage; comet assay; TEL/ABL; HL-60;
D O I
10.1016/S0145-2126(02)00051-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Human lymphocytes, p53 protein-deficient acute promyelocytic leukemia cell line HL-60, murine pro-B lymphoid cell line BaF3 and its TEL/ABL-transformed clone cells were exposed to idarubicin with and without pre-treatment with amifostine. Idarubicin at 0.5-5 muM evoked DNA damage measured by the Comet assay. Amifostine at 14 mM decreased DNA-damaging effect of idarubicin in human lymphocytes and BaF3 cells, but increased the effect in TEL/ABL-transformed cells. Amifostine had no influence on the action of idarubicin in HL-60 cells. Our results suggest that the reaction of the cell to DNA damage may contribute to its diverse response to amifostine combined with anticancer drugs and that p53 and fusion tyrosine kinases may be involved in this diversity. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1093 / 1096
页数:4
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