期刊文献+

电离辐射对小鼠EL-4淋巴瘤细胞P21蛋白表达的影响 被引量:6

Effects of ionizing radiation on the expression of P21 protein in EL-4 mouse lymphoma cells
原文传递
导出
摘要 目的阐明电离辐射对小鼠EL-4淋巴瘤细胞P21蛋白表达的影响。方法采用免疫细胞化学方法和流式细胞术检测X射线照射对P21蛋白表达的时程和量效变化的影响。结果时程实验结果显示,离体培养的EL-4细胞经4.0Gy X射线照射后,P21蛋白表达在2~72h(免疫细胞化学方法检测)和8~72h(流式细胞术检测)明显增高(分别为P<0.01、P<0.001)。量效实验结果显示,X射线照射后24h,P21蛋白表达在0.5~6.0Gy(免疫细胞化学方法检测)和1.0~4.0Gy(流式细胞术检测)明显增高(分别为P<0.05、P<0.01、P<0.001)。结论X射线能诱导P21蛋白表达增高,在一定范围内存在时间和剂量依赖关系。 Objective To explore the effects of ionizing radiation on the expression of P21 protein. Methods Immunocytochemistry and flow cytometry were used to measure the changes in the expression of P21 protein in EL-4 cells along with the increment of time and radiation doses. Results After 4.0 Gy X-rays irradiation, marked elevation of P21 protein level was found in EL-4 cells at 2-72 h with immunocytochemical method and at 8-72 h with flow cytometry (P 〈 0.01 or P 〈 0.001, respectively). On the other hand, it was observed that the level of P21 protein increased evidently with the delivery of 0.5-6.0 Gy X-rays by using immunocytochemical method and with the delivery of 1.0-4.0 Gy X-rays by using flow cytometry in EL-4 cells at 24 h after irradiation. Conclusion The P21 protein expression could be increased by X-irradiation in time- and dose-dependent manners.
出处 《中华放射医学与防护杂志》 CAS CSCD 北大核心 2005年第6期514-516,共3页 Chinese Journal of Radiological Medicine and Protection
基金 国家自然科学基金资助项目(30270346)
关键词 电离辐射 EL-4淋巴瘤细胞 P21 蛋白表达 Ionizing radiation EL-4 mouse lymphoma cells P21 Protein expression
  • 相关文献

参考文献1

二级参考文献12

  • 1朱明华,王文亮.肿瘤抑制基因p53突变与原发性肝癌的关系[J].中华肿瘤杂志,1993,15(4):245-247. 被引量:9
  • 2Feitelson MA,Zhu M,Duan LX,et al.Hepatitis B x antigen and p53 are associated in vitro and in liver tissues from patients with primary hepatocellular carcinoma [J].Oncogene,1993,8:1109-1117.
  • 3Ahn JY,Jung EY,Kwun HJ,et al.Dual effects of hepatitis B virus X protein on the regulation of cell cycle control depending on the status of cellular p53[J].J Gen Virol,2002,83(Pt 11):2765-2772.
  • 4El-deiry WS,Tokino T,Velculescu VE,et al.WAF1,a potential mediator of p53 tumor suppression [J].Cell,1993,75:817-825.
  • 5Ahn JY,Chung EY,Kwun HJ,et al.Transcriptional repression of p21(waf1) promoter by hepatitis B virus X protein via a p53 independent pathway [J].Gene,2001,275:163-168.
  • 6Kang MS,Lee HJ,Lee JH,et al.Mutation of p53 gene in hepatocellular carcinoma cell lines with HBX DNA [J].Int J Cancer,1996,67:898-902.
  • 7Sohn S,Jaitovitch-Groisman I,Benlimame N,et al.Retroviral expression of the hepatitis B virus x gene promotes liver cell susceptibility to carcinogen induced site specific mutagenesis [J].Mutat Res,2000,460:17-28.
  • 8Groisman IJ,Koshy R,Henkler F,et al.Downregulation of DNA excision repair by the hepatitis B virus-x protein occurs in p53 proficient and p53 deficient cells [J].Carcinogenesis,1999,20:479-483.
  • 9Shintani Y,Yotsuyanagi H,Moriya K,et al.Induction of apoptosis after switch-on of the hepatitis B virus X gene mediated by the Cre/loxP recombination system [J].J Gen Virol,1999,80 (Pt 12):3257-3265.
  • 10Elmore LW,Hancock AR,Chang SF,et al.Hepatitis B virus X protein and p53 tumor suppressor interactions in the modulation of apoptosis [J].Proc Natl Acad Sci USA,1997,94:14707-14712.

共引文献8

同被引文献42

引证文献6

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部