Comparative cytotoxicity of dimethylamide-crotonin in the promyelocytic leukemia cell line (HL60) and human peripheral blood mononuclear cells

被引:61
作者
Anazetti, MC
Melo, PS
Durán, N
Haun, M
机构
[1] Univ Estadual Campinas, Inst Biol, Dept Bioquim, BR-13083970 Campinas, SP, Brazil
[2] Univ Estadual Campinas, Inst Quim, Lab Quim Biol, BR-13083970 Campinas, SP, Brazil
[3] Univ Mogi das Cruzes, NCA, Cruzes, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
apoptosis; cell differentiation; dehydrocrotonin; dimethylamide-crotonin; HL60; cells; human peripheral blood mononuclear;
D O I
10.1016/S0300-483X(03)00089-1
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Dehydrocrotonin (DHC) is a diterpene lactone obtained from Croton cajucara (Sacaca). Dimethylamide-crotonin (DCR), a DHC derivative, has a similar inhibitory effect on leukemic HL60 cells than its parent compound evaluated by different endpoints of cytotoxicity. No cytotoxicity or morphological alterations associated with apoptosis were detected in human peripheral blood mononuclear cells (PBMC) after treatment with up to 400 muM DCR in presence of phytohemaglutinin (5 mug/ml). Based on morphological changes and the pattern of DNA fragmentation, DHC and DCR were found to induce apoptosis and terminal differentiation (assessed by nitro blue tetrazolium reduction) in HL60 cells, but these compounds did not show any toxic effect in PBMC. Thus, DCR and DHC inhibit HL60 cell growth in vitro partly by inducing apoptosis and cell differentiation, but does not cause serious damage to immune cells according to our experimental conditions. (C) 2003 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:261 / 274
页数:14
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