首页 | 本学科首页   官方微博 | 高级检索  
     检索      

姜黄素对食管癌细胞系放射敏感性的影响及其机理
引用本文:张晓智,韩苏夏,杨玉琮,李旭.姜黄素对食管癌细胞系放射敏感性的影响及其机理[J].西安交通大学学报(医学版),2003,24(4):377-378,386.
作者姓名:张晓智  韩苏夏  杨玉琮  李旭
作者单位:1. 西安交通大学第一医院肿瘤放疗科,陕西西安,710061
2. 西安交通大学第一医院实验医学中心,陕西西安,710061
基金项目:陕西省中医药管理局科研基金资助 (No .2 0 0 1 0 54)
摘    要:目的 探讨姜黄素对食管癌细胞系Eca10 9的放射增敏作用及其机制。方法 利用细胞克隆技术进行剂量 -存活曲线分析 ,末端脱氧核苷酰转移酶法检测细胞凋亡 ,并对细胞周期进行分析。结果 姜黄素组D0 值为 91.35cGy ,空白对照和空白药物组D0 值分别为 130 .0 7cGy和 138.37cGy ,(P <0 .0 5 )。流式细胞仪分析空白组和姜黄素组凋亡区阳性细胞分别为 1.0 1%和 87.5 8% (P <0 .0 5 ) ;经姜黄素处理后 ,与对照组相比 ,G0 1 期细胞比例降低 ,G2 + M期细胞比例增高。结论 姜黄素可以明显提高Eca 10 9细胞的放射敏感性 ,机制可能与其引起瘤细胞周期阻滞 ,诱导肿瘤细胞凋亡有关

关 键 词:姜黄素  食管癌  放射敏感性  放射治疗
文章编号:1671-8259(2003)04-0377-02

The influence of curcumin on the radiosensitivity of esophageal carcinoma cell lines and its mechanism
Zhang Xiaozhi,Han Suxia,Yang Yucong,Li Xu.The influence of curcumin on the radiosensitivity of esophageal carcinoma cell lines and its mechanism[J].Journal of Xi‘an Jiaotong University:Medical Sciences,2003,24(4):377-378,386.
Authors:Zhang Xiaozhi  Han Suxia  Yang Yucong  Li Xu
Abstract:Objective To investigate the influence of curcumin on the radiosensitivity of esophageal carcinoma cell lines (Eca109) and its mechanism. Methods The colony formation ability of Eca109 cells after X-ray irradiation was analyzed by linear-quadratic formulation. The apoptotic percentage was measured by TUNEL and cell cycle was analyzed by FCM. Results The D 0 value of Eca109 cell lines was 97.35?cGy, and that of control group and free-curcumin group was 130.07cGy and 138.37?cGy, respectively (P< 0.05). The apoptotic percentage of Eca109 cell lines exposed to free-medicine and curcumin group was 1.01% and 87.58%, respectively (P< 0.05). In curcumin group the percentage of cells in G 2+M phase increased. Conclusion Curcumin can increase the radiosensitivity of esophageal carcinoma cell lines, which may be associated with blocking cell cycle and inducing apoptosis of Eca109 cells.
Keywords:curcumin  esophageal carcinoma  radiosensitivity  radiotherapy
本文献已被 CNKI 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号