Applying fluorescence lifetime imaging microscopy to evaluate the efficacy of anticancer drugs

被引:11
作者
Kawanabe, Satoshi [1 ]
Araki, Yoshie [1 ]
Uchimura, Tomohiro [1 ,2 ,3 ]
Imasaka, Totaro [1 ,2 ]
机构
[1] Kyushu Univ, Grad Sch Engn, Dept Appl Chem, Nishi Ku, Fukuoka 8190395, Japan
[2] Kyushu Univ, Ctr Future Chem, Dept Translat Res Ctr, Nishi Ku, Fukuoka 8190395, Japan
[3] Univ Fukui, Grad Sch Engn, Dept Mat Sci & Engn, Fukui 9108507, Japan
来源
METHODS AND APPLICATIONS IN FLUORESCENCE | 2015年 / 3卷 / 02期
关键词
FLIM; doxorubicin; epirubicin; SYTO; 13; DYE-LASER; CELLS; APOPTOSIS; CYTOMETRY; DNA; DOXORUBICIN; PROBES; FLIM;
D O I
10.1088/2050-6120/3/2/025006
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Fluorescence lifetime imaging microscopy was applied to evaluate the efficacy of anticancer drugs. A decrease in the fluorescence lifetime of the nucleus in apoptotic cancer cells stained by SYTO 13 dye was detected after treatment with antitumor antibiotics such as doxorubicin or epirubicin. It was confirmed that the change in fluorescence lifetime occurred earlier than morphological changes in the cells. We found that the fluorescence lifetime of the nucleus in the cells treated with epirubicin decreased more rapidly than that of the cells treated with doxorubicin. This implies that epirubicin was more efficacious than doxorubicin in the treatment of cancer cells. The change in fluorescence lifetime was, however, not indicated when the cells were treated with cyclophosphamide. The decrease in fluorescence lifetime was associated with the processes involving caspase activation and chromatin condensation. Therefore, this technique would provide useful information about apoptotic cells, particularly in the early stages.
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页数:6
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