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Egr-1启动子辐射诱导的基因表达特性

The Property of Egr-1 Promoter in Irradiation-Induced Gene Expression
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摘要 目的:研究电离辐射作用下早期生长反应因子1(Egr-1)启动子调控增强绿色荧光蛋白(EGFP)报告基因在人结肠癌细胞SW480中的表达。方法:利用基因重组手段构建质粒Egr-1-EGFP;阳离子脂质体介导转染人结肠癌细胞SW480,给予不同剂量γ射线照射,流式细胞仪检测照射后不同时间点EGFP的表达。结果:电离辐射能够诱导Egr-1启动子调控下游基因的表达,且6 Gy照射后最为明显,在照射后24 h达到高峰。结论:Egr-1启动子具有电离辐射诱导特性。 Objective: To study the effect of ionizing radiation on the expression of EGFP reporter gene induced by Egr-1 promoter in human colorectal adenocarcinoma cell line SW480. Methods: The plasmid Egr-1-EGFP was constructed by gene recombination, and was transfected into the SW480 cells with cationic liposome, then the cells were treated with various doses of γ-ray irradiation. FACS was used to detect the EGFP expression at different times after exposure. Results: FACS analysis showed that ionizing radiation could induce the expression of EGFP report gene, and this expression reached maximum at 24 h post 6 Gy γ-ray exposure. Conclusion: Egr-1 gene promoter has ionizing radiation-inducible characteristics.
出处 《武汉大学学报(医学版)》 CAS 2008年第2期186-189,共4页 Medical Journal of Wuhan University
基金 湖北省科技攻关项目(编号:2005AA304B04)
关键词 EGR-1启动子 增强绿色荧光蛋白 基因表达 电离辐射 EGR-1 Promoter Enhanced Green Fluorescence Protein Gene Expression l-onizing Radiation
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  • 1Marples B, Greco O, Joiner MC, et al. Molecular approaches to chemo-radio therapy[J]. Eur J cancer,2002, 38(2): 231-239.
  • 2Weichselbaum RR, Hallahan DE, Beckett MA, et al. Gene therapy targeted by radiation preferentially radio- sensitizes tumor cells[J]. Cancer Res, 1994, 54 (16): 4266-4269.
  • 3Scott SD, Joiner MC, Marples B. Optimizing radiation- responsive gene promoters for radio-genetic cancer therapy [J]. Gene therapy,2002, 9(20): 1396-1402.
  • 4Ahmed MM. Regulation of radiation- induced apoptosis by early growth response-1 gene in solid tumors[J]. Curr Cancer Drug Targets, 2004, 4(1) : 43-52.
  • 5Wang WD, Chen ZT, Li R, et al. Enhanced efficacy of radiation-induced gene therapy in mice bearing lung adenocarcinoma xenografts using hypoxia responsive elements[J]. Cancer Sci, 2005, 96 (12): 918-924.
  • 6Anton M, Gomaa IE, von Lukowicz T, et al. Optimization of radiation controlled gene expression by adeno- viral vectors in vitro [J]. Cancer Gene Ther, 2005, 12 (7) : 640-646.
  • 7Marples B, Scott SD, Hendry JH, et al. Development of synthetic promoters for radiation-mediated gene therapy[J]. GeneTher, 2000, 7(6): 511-517.
  • 8Weichselbaum RR, Kufe DW, Advani SJ, et al. Molecular targeting of gene therapy and radiotherapy[J]. Acta Oncol, 2001, 40(6): 735-738.
  • 9Joki T, Nakamura M, Ohno T. Activation of the radiosensitive EGR-1 promoter induces expression of the herpes simplex virus thymidine kinase gene and sensitiveity of human glioma cells to ganciclovir [J]. Hum Gene Ther, 1995, 6(12): 1507-1513.
  • 10Manome Y, Kunieda T, Wen PY, et al. Transgene expression in malignant glioma using a replication-defective adenoviral vector containing the Egr-1 promoter: activation by ionizing radiation or uptake of radioactive iododeoxyuridine [J]. Hum Gene Ther, 1998, 9(10): 1409-1417.

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