基础医学与临床 ›› 2013, Vol. 33 ›› Issue (7): 808-813.

• 研究论文 • 上一篇    下一篇

沉默H2AX食管癌ECA109中MDC1和53BP1斑点的变化

史鸿云1,祝淑钗2,刘志坤3,苏景伟3   

  1. 1. 河北大学附属医院
    2. 河北医科大学第四医院放疗科
    3. 河北医科大学第四医院
  • 收稿日期:2012-08-13 修回日期:2012-09-24 出版日期:2013-07-05 发布日期:2013-06-26
  • 通讯作者: 史鸿云 E-mail:hyshi2012@sina.com
  • 基金资助:
    H2AX、STAT1蛋白表达调控体内外食管癌细胞放射敏感性的研究

The impact to MDC1 and 53BP1 after silence H2AX in esophageal carcinomas ECA109

  • Received:2012-08-13 Revised:2012-09-24 Online:2013-07-05 Published:2013-06-26
  • Contact: Hong-yun SHI E-mail:hyshi2012@sina.com

摘要: 目的 探讨沉默H2AX后在食管高分化鳞状细胞癌ECA109细胞中应答电离辐射时对MDC1和53BP1的影响。方法 构建沉默H2AX的慢病毒载体,将慢病毒转染食管癌ECA109细胞并检测转染后的沉默效用;免疫荧光检测r-H2AX、MDC1和53BP1核内斑点的情况以及用western blot检测这几种蛋白的表达。结果 1)成功构建了沉默H2AX的 ECA109细胞。2)电离辐射可引起r-H2AX表达量的增加,不引起MDC1和53BP1表达的增加,同时电离辐射诱导产生的r-H2AX、MDC1和53BP1核内斑点变化的规律一致。3)沉默H2AX后的ECA109细胞核内r-H2AX、MDC1和53BP1斑点的数量明显减少,尽管MDC1和53BP1蛋白表达无变化。结论 在ECA109细胞中H2AX是电离辐射后比较早的反应蛋白,可以调节下游MDC1和53BP1斑点的位置。

关键词: 食管癌, r-H2AX, MDC1, 53BP1, 核内斑点

Abstract: Objective To discover the impact to MDC1 and 53BP1 after silence H2AX and when ionizing radiation in esophageal high grade squamous cell carcinoma ECA109. Methods Construction of lentiviral vector silencing H2AX , then transfecting lentivirus to esophageal cancer ECA109 and detecting the silence effect after transfection. Immunofluorescence detection the nuclear focus of r-H2AX、MDC1 and 53BP1 in ECA109 with ionizing radiation before and after transfection. As well as detection the expression of three proteins by western blot. Results 1) Successfully constructed the silence of H2AX in ECA109 cells. 2) Ionizing radiation can cause r-H2AX expression increases but not MDC1 and 53BP1. Ionizing radiation-induced nuclear focus of r-H2AX, MDC1 and 53BP1 are similar. 3) The nucleus focus of r-H2AX, MDC1 and 53BP1 are significantly reduced in ECA109 after silence H2AX. Protein expression did not change. Conclusion H2AX is one of early ionizing radiation-reaction protein in ECA109 and is located in the damage response upstream and can adjust the position of MDC1 and 53BP1.

Key words: Esophageal carcinoma, HistoneH2AX-PhosPhorylation, MDC1, 53BP1, Nuclear foci

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