Induction of apoptosis in human leukaemia HL-60 cells by furanone-coumarins from Murraya siamensis

被引:10
|
作者
Murata, Tomiyasu [1 ]
Itoigawa, Masataka [2 ]
Ito, Chihiro [1 ]
Nakao, Keisuke [1 ]
Tsuboi, Masaru [1 ]
Kaneda, Norio [1 ]
Furukawa, Hiroshi [1 ]
机构
[1] Meijo Univ, Fac Pharm, Tempaku Ku, Nagoya, Aichi 8503, Japan
[2] Tokai Gakuen Univ, Fac Human Wellness, Tempaku Ku, Nagoya, Aichi 4688514, Japan
关键词
D O I
10.1211/jpp.60.3.0015
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
To identify potential anti-tumour agents, we screened five furanone-coumarins isolated from Murraya siamensis Craib (Rutaceae) for their ability to inhibit the growth of human leukaemia HL-60 cells. Among the furanone-coumarins tested, murrayacoumarin B (compound 2) showed significant cytotoxicity against HL-60 cells. Fluorescence microscopy with Hoechst 33342 staining revealed that the percentage of apoptotic cells with fragmented nuclei and condensed chromatin increased in a time-dependent manner after treatment with murrayacoumarin B. Interestingly, this furanone-coumarin induced the loss of the mitochondrial membrane potential. In addition, treatment with murrayacoumarin B stimulated the activities of caspase-9 and caspase-3, and caspase-9 and caspase-3 inhibitors suppressed the apoptosis induced by murrayacoumarin B. These results suggest that murrayacoumarin B induced apoptosis in HL-60 cells through activation of the caspase-9/caspase-3 pathway triggered by mitochondrial dysfunction.
引用
收藏
页码:385 / 389
页数:5
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