童流妹,冯丽波,陆雪官,陈列松,郭信伟,田野.微环境乏氧通过肿瘤干细胞途径对脑胶质瘤细胞放射敏感性的影响[J].中华放射医学与防护杂志,2010,30(2):165-168
微环境乏氧通过肿瘤干细胞途径对脑胶质瘤细胞放射敏感性的影响
Effect of microenviroment hypoxia on glioma cells radiosensitivity through cancer stem cell pathway
投稿时间:2009-08-18  
DOI:
中文关键词:  胶质瘤细胞  乏氧  肿瘤干细胞  HIF-1α  Notch 1
英文关键词:Glioma  Hypoxia  Cancer stem cell  HIF-1α  Notch 1
基金项目:江苏省自然科学基金面上项目(BK2009126);江苏省高校自然科学基金项目(09KJB320012)
作者单位E-mail
童流妹 215004,苏州大学附属第二医院肿瘤放射治疗科  
冯丽波 215004,苏州大学附属第二医院肿瘤放射治疗科  
陆雪官 215004,苏州大学附属第二医院肿瘤放射治疗科 luxueguanok@yahoo.com.cn 
陈列松 215004,苏州大学附属第二医院肿瘤放射治疗科  
郭信伟 215004,苏州大学附属第二医院肿瘤放射治疗科  
田野 215004,苏州大学附属第二医院肿瘤放射治疗科  
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中文摘要:
      目的 探讨微环境乏氧是否能通过肿瘤干细胞途径引起脑胶质瘤放射敏感性的改变以及可能的相关机制。方法 选择脑胶质瘤SHG44和U251细胞株分别在常氧(20% O2)、乏氧(1% O2)12和24 h的条件下培养后,应用流式细胞仪检测CD133表达阳性细胞的比例,细胞克隆形成实验绘制细胞存活曲线以观察其放射敏感性,采用Western blotting方法测定基因HIF-1α及其下游基因Notch 1蛋白的表达水平。结果 与常氧培养条件比,SHG44和U251细胞乏氧12和24 h后CD133阳性表达比例明显升高;SF2(2 Gy照射时的存活分数)均升高。在乏氧12和24 h培养时,SHG44细胞株的氧增强比的值分别为1.54和1.38,而U251细胞株则分别为1.44和1.23,提示在乏氧培养时细胞的放射敏感性下降;与常氧培养条件比,乏氧时HIF-1α和Notch 1的蛋白表达水平均明显升高。结论 微环境乏氧能通过提高肿瘤干细胞的比例而降低脑胶质瘤细胞的放射敏感性,其可能的作用信号途径为HIF-1α - Notch 1。
英文摘要:
      Objective To investigate the effect of microenviroment hypoxia on glioma cells radiosensitivity through cancer stem pathway, and to explore the related mechanism. Methods Glioma cell lines SHG44 and U251 were cultured in normoxia(20% O2) or continuous hypoxia(1% O2)for 12 and 24 h. The fraction of glioma cells with positive expression of CD133 was assayed by flow cytometry. The radiosensitivity of glioma cells was determined by clonogenic cell assay. Western blotting was used to investigate the expressions of HIF-1α and its downstream gene Notch 1. Results The fraction of glioma cells with positive expression of CD133 was higher after hypoxic culture for 12 and 24 h than that of the corresponding cells cultured in normoxia. Compared to the cells cultured in normoxia, SF2 (survival fraction at 2 Gy) were enhanced significantly in SHG44 and U251 cells cultured in hypoxia for 12 and 24 h. The OER (oxygen-enhancement ratio) of SHG44 cells in hypoxia for 12 and 24 h was 1.54 and 1.38, respectively. The OER of U251 cells was 1.44 and 1.23, respectively. The radiosensitivity of these two cell line was decreased in hypoxia. The protein expressions of HIF-1α and Notch1 genes were elevated more significantly for cells cultured in hypoxia for 12 and 24 h than for those in normoxia. Conclusions Microenviroment hypoxia could increase the radioresistance of glioma cells through enrichment of cancer stem cella, and HIF-1α - Notch1 signal pathway may play an important role in this process.
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