纪蓉,曹建平,陈遐林,朱巍,江庆,潘春燕,周媛媛,封阳,彭晓梅,刘杨,樊赛军.青蒿琥酯对人宫颈癌HeLa细胞的放射增敏作用[J].中华放射医学与防护杂志,2010,30(5):554-557
青蒿琥酯对人宫颈癌HeLa细胞的放射增敏作用
Study of radiation sensitization of artesunate on human HeLa cells of cervical cancer
投稿时间:2009-11-30  
DOI:
中文关键词:  放射增敏  青蒿琥酯  HeLa细胞  细胞凋亡
英文关键词:Radiosensitization  Artesunate  HeLa cell  Apoptosis
基金项目:国家自然科学基金(30670632); 教育部长江学者和创新团队发展计划资助项目(IRT0849)
作者单位E-mail
纪蓉 215123 苏州大学医学部放射医学与公共卫生学院 江苏省放射医学与防护重点实验室  
曹建平 215123 苏州大学医学部放射医学与公共卫生学院 江苏省放射医学与防护重点实验室 jpcao@suda.edu.cn 
陈遐林 浙江省绍兴市人民医院放疗科  
朱巍 215123 苏州大学医学部放射医学与公共卫生学院 江苏省放射医学与防护重点实验室  
江庆 215123 苏州大学医学部放射医学与公共卫生学院 江苏省放射医学与防护重点实验室  
潘春燕 215123 苏州大学医学部放射医学与公共卫生学院 江苏省放射医学与防护重点实验室  
周媛媛 215123 苏州大学医学部放射医学与公共卫生学院 江苏省放射医学与防护重点实验室  
封阳 215123 苏州大学医学部放射医学与公共卫生学院 江苏省放射医学与防护重点实验室  
彭晓梅 吴江市疾病预防控制中心  
刘杨 苏州市市立医院  
樊赛军   
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中文摘要:
      目的 探讨青蒿琥酯对人宫颈癌HeLa细胞的放射增敏作用。方法 应用60Co γ射线照射细胞,吸收剂量率为0.635 Gy/min,照射剂量为0、1、2、4和6 Gy。采用MTT法检测青蒿琥酯对HeLa细胞的抑制作用,确定青蒿琥酯的最适实验作用浓度。克隆形成法检测青蒿琥酯对HeLa细胞放射敏感性的影响;采用"多靶单击数学模型"拟合HeLa细胞的剂量-存活曲线,得出平均致死剂量、准阈剂量及放射增敏比,评价其增敏效果。用流式细胞术检测HeLa细胞凋亡率,进一步检测青蒿琥酯对HeLa细胞的放射增敏性。结果 青蒿琥酯对HeLa细胞的抑制作用随药物浓度的增加而增加,单纯照射1、2、4和6 Gy细胞的克隆形成率分别为91.67%、82.02%、58.60%和25.01%,加入青蒿琥酯后,相同照射剂量下克隆形成率分别降低为74.93%、60.53%、22.38%和5.05%;单纯照射组与药物+照射组的平均致死剂量(D0)分别为2.95和2.07 Gy,准阈剂量(Dq)分别为2.01和1.24 Gy,放射增敏比(SER)为1.43。单纯2和6 Gy照射组细胞凋亡率分别是12.26%和40.08%,加入青蒿琥酯后,相同照射剂量下细胞凋亡率分别上升至22.71%和59.92%。结论 青蒿琥酯对人宫颈癌HeLa细胞的抑制作用成药物浓度依赖性;青蒿琥酯对HeLa细胞具有一定的放射增敏作用。
英文摘要:
      Objective To investigate the radiosensitizing effects of artesunate on human HeLa cells of cervical cancer in vitro. Methods Hela cells were irradiated with 60Co γ-rays. The dose rate was 0.635 Gy/min and the radiation dose was 0,1,2,4,6 Gy, respectively. The anti-proliferation activities of artesunate on HeLa cells were evaluated with MTT assay, to determine the most appropriate drug concentration. The effect of radiosensitivity was observed by using clonogenic assay. The single-hit multi-target model was used to plot the HeLa cell’s dose-survival curve, to calculate mean lethal dose, quasi-threshold dose and sensitization enhancement rate, and to evaluate its radiosensitization effect. The apoptosis was analyzed with flow cytometry (FCM) to further test the radiation senseitization of artesunate on HeLa cells. Results The inhibition of artesunate on HeLa cells increased with concentration. In radiation group, the cell cloning efficiency were 91.67%, 82.02%, 58.60%, 25.01%, respectively, and in artesunate (2.0 μmol/L) +radiation group, the cell cloning efficiency were 74.93%, 60.53%, 22.38%, 5.05%. In radiation group and artesunate (2.0 μmol/L) +radiation group, the mean lethal dose(D0 was 2.95 and 2.07 Gy, respectively, while the qusai-threshold dose (D</em>q) were 2.01 and 1.24 Gy,respectively, and SER was 1.43. Compared with 2 and 6 Gy radiation group, the apoptosis rate of drug + radiation group increased from 12.26%, 40.08% to 22.71%, 59.92%. Conclusions The inhibiting effect of artesunate on HeLa cells is concentration-dependent. Artesunate has radiosensitizing effect on HeLa cells in vitro.
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