Cell filling and radiosensitization by caffeic acid phenethyl ester (CAPE) in lung cancer cells

被引:79
作者
Chen, MF
Wu, CT
Chen, YJ
Keng, PC
Chen, WC [1 ]
机构
[1] Chang Gung Mem Hosp, Dept Radiat Oncol, Chiayi, Taiwan
[2] Chang Gung Univ, Inst Clin Med Sci, Linkou, Taiwan
[3] Chang Gung Mem Hosp, Dept Urol, Linkou, Taiwan
[4] Mackay Mem Hosp, Dept Radiat Oncol, Taipei, Taiwan
[5] Univ Rochester, Sch Med & Dent, Dept Radiat Oncol, Rochester, NY USA
关键词
CAPE and radiation; lung cancer; apoptosis; G2; arrest; radiation sensitization;
D O I
10.1269/jrr.45.253
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Caffeic acid phenethyl ester (CAPE) is a biologically active ingredient of honeybee propoplis. The cytotoxicity and radiation sensitization effects of CAPE were evaluated in human lung cancer A549 cells and normal lung fibroblast WI-38 cells. A549 cells treated with 6 mug/ml CAPE showed marked growth inhibition (60%) at 48 hr after treatments. During the same time, the number of viable cells decreased to 46% of the control value. In contrast, WI-38 cells showed 20% growth inhibition with no change in the number of viable cells under the same treatment conditions. At 72 hr after CAPE treatment (6 mug/ml), the percentage of apoptotic cells in A549 cultures increased significantly to 67% and an S/G2 arrest was also detected in the culture. Furthermore, there was a significant decrease in the level of intracellular glutathione and hydrogen peroxide contents within one hr after CAPE treatment, and the expression of cyclin B1 was reduced 6 hr after treatment. The radiation sensitization effect of CAPE on A549 cells was determined from the clonogenic survival curves, and the results showed a small but significant difference in radiation survival between cells treated with or without CAPE. Taken together, our results suggest that the effects of CAPE on differential cytotoxicity, apoptosis, and radiosensitization are associated with glutathione depletion that occurred shortly after treatments.
引用
收藏
页码:253 / 260
页数:8
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