王小强,曹建平,樊赛军,朱巍,黄晓菲,刘杨,陈遐林,宫晓梅,彭晓梅,曾静.咖啡酸苯一酯对人宫颈癌HeLa细胞的放射增敏作用[J].中华放射医学与防护杂志,2009,29(2):136-138
咖啡酸苯一酯对人宫颈癌HeLa细胞的放射增敏作用
Radiation sensitization by CAPE on human HeLa cells of cervical cancer
投稿时间:2008-03-04  
DOI:10.3760/cma.j.issn.0254-5098.2009.02.004
中文关键词:  咖啡酸苯一酯  放射增敏作用  周期检查点  电离辐射
英文关键词:Caffic acid phenethyl ester  Radiosensitizing effect  Cycle checkpoint  Ionizing radiation
基金项目:国家自然科学基金(30670632)
作者单位E-mail
王小强 215123 苏州大学放射医学与公共卫生学院放射生物学教研室  
曹建平 215123 苏州大学放射医学与公共卫生学院放射生物学教研室 jpcao@suda.edu.cn 
樊赛军 215123 苏州大学放射医学与公共卫生学院放射生物学教研室  
朱巍 215123 苏州大学放射医学与公共卫生学院放射生物学教研室  
黄晓菲 215123 苏州大学放射医学与公共卫生学院放射生物学教研室  
刘杨 215123 苏州大学放射医学与公共卫生学院放射生物学教研室  
陈遐林 215123 苏州大学放射医学与公共卫生学院放射生物学教研室  
宫晓梅 215123 苏州大学放射医学与公共卫生学院放射生物学教研室  
彭晓梅 215123 苏州大学放射医学与公共卫生学院放射生物学教研室  
曾静 215123 苏州大学放射医学与公共卫生学院放射生物学教研室  
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中文摘要:
      目的 探讨咖啡酸苯一酯(CAPE)对人宫颈癌HeLa细胞的放射增敏作用。方法 将宫颈癌HeLa细胞经不同浓度的CAPE作用24 h,四甲基偶氮唑盐比色法(MTT)法检测细胞抑制效应与CAPE浓度的关系。将HeLa细胞设对照组和药物组,两组均经60Coγ射线照射0、2、4、6和8 Gy,计数细胞克隆;另将HeLa细胞设对照组、CAPE组、单纯照射组、照射+CAPE组,流式细胞检测技术分析CAPE对细胞周期的影响。结果 CAPE对HeLa细胞的抑制率呈剂量依赖性增加(F=126.49~3654.88,P<0.01);细胞经60Coγ射线照射后,HeLa细胞克隆存活率随着照射剂量的增加而降低(F=174.42~9422.81,P<0.01);相同剂量下,药物组的HeLa细胞克隆存活率低于对照组(F=120.14~251.91,P<0.01);药物组和对照组HeLa细胞的平均致死剂量(D0)为1.45和1.82 Gy、准阈剂量(Dq)为1.89和3.21 Gy, 药物组较小,放射增敏比(SER)为1.26>1;与对照组相比, CAPE组及单纯照射组G2/M期的细胞比例升高(P<0.01),而在照射+CAPE组则降低(P<0.01)。结论CAPE通过对人宫颈癌HeLa细胞G2/M期的阻滞及可能抑制细胞亚致死性损伤修复能力,发挥放射增敏作用。
英文摘要:
      Objective To study the radiosensitizing effect of caffic acid phenethyl ester (CAPE) on human cervical cancer HeLa cells.Methods MTT assay was used to measure the relation between the inhibition effect and CAPE concentrations by CAPE with different concentrations on HeLa cells for 24 hours. HeLa cells were divided into the control and experimental groups,both of which were given 0, 2, 4, 6 and 8 Gy of 60Coγ-irradiation, respectively. The cell clones were counted. Meanwhile HeLa cells were divided into the control, CAPE, irradiation and combination groups. Flow cytometric analysis was adopted to detect the changes of cell cycle distribution induced by CAPE.Results The inhibition rate of CAPE acting on Hela cells increased with concentrations(F=126.49~3654.88,P<0.01).HeLa cells cloning survival decreased with the increase of radiation dose(F=174.42~9422.81,P<0.01).At the same radiation dose, HeLa cells cloning survival was less in experimental group than control group(F=120.14~251.91,P<0.01). The mean lethal dose(D0)(1.45 and 1.82 Gy) and the quasi-threshold dose(Dq) (1.89 and 3.21 Gy) of HeLa cells in experimental group decreased comparing with control group,SER was 1.26. Compared with the sole irradiation group, cells in G2/M phase of the CAPE group and the sole irradiation group increased (P<0.01) while the combination group decreased (P<0.01).Conclusion CAPE could increase the radiation sensitivity of HeLa cells by G2/M arrest and may be related to the inhibition of the sub-lethal damage repair.
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