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辐射诱导Egr-1调控腺病毒介导Trail基因体外表达及意义 被引量:1

Expression property of Ad-Egr-hTrail induced by ionizing radiation
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摘要 目的探讨不同辐射剂量X射线照射对转染重组腺病毒(Ad-Egr-hTrail)的胶质瘤U251细胞hTrailmRNA表达的影响。方法扩增Ad-Egr-hTrail。将扩增鉴定成功的Ad-Egr-hTrail感染U251细胞,感染48 h后分别予0、2、5、8、10、12、15、18 Gy X射线照射,real-time quanitative-PCR法测定不同剂量照射后肿瘤细胞中Trail mRNA表达。结果 U251细胞TrailmRNA表达水平照射后1 h开始升高,4~8 h维持在较高表达水平,照射后4 h表达水平最高,随后开始下降;随照射剂量增加,Trail mRNA表达水平明显增加,12 Gy时达到最高水平,然后随照射剂量增加,表达水平开始下降。结论重组腺病毒经射线诱导Egr-1基因启动子能够调控Trail基因体外表达,Trail基因表达量与放射剂量及放射后间隔时间有关。 Objective To investigate the effects of different doses of X-ray radiation on the expression of hTrail mRNA of glioma U251 cells which transfected Ad-Egr-hTrail.Methods Ad-Egr-hTrail was identitied by RT-PCR after amplification and transfected U251 cells,X-ray of 0,2,5,8,10,12,15,18 Gy was given 48 h after the transfection,the expression level of TrailmRNA was detected by real-time quantitative-PCR.Results The expressed level of TrailmRNA started to increase at 1hour post-irradiation,and maintained a high level from 4 hour to 8 hour.The expressed level of TrailmRNA increased with the radiation dose increasing,and rase the highest at the the point of 12Gy point,then began to descend.Conclusion Egr-1 promoter can be activated by ionizing irradiation and regulate the expression of Trail gene in vitro.The expression of Trail gene is correlated with radiation dose and time interval after irradiation.
出处 《山东医药》 CAS 北大核心 2011年第19期15-17,共3页 Shandong Medical Journal
基金 国家自然科学基金资助项目(30770916) 徐州市科技项目(XF10C078)
关键词 辐射诱导 胶质瘤U251细胞 放射治疗 Egr-1 promoter radiation induction glioma U251 cells radiotherapy
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  • 1Zhang WW, Fang X, Branch CD, et al. Generation and identification of recombinant adenovlms by liposome2mediated transfecfion and PCRanalysis[J]. Bioteclmiques, 1993,15(5) :868-872.
  • 2Hori T, Kondo T, Kanamori M, et al. Ionizing radiation enhances tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) -induced apoptosis through up-regulations of death receptor 4 (DR4) and death receptor 5 (DRS) in human osteosarcoma cells[J]. J Orthop Res, 2010,28(6) :739-745.
  • 3Tsurushima H, Yuan X, Dillehay LE, et el. Radioresponsive tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) gene therapy for malignant brain tumors[ J]. Cancer Gene Ther, 2007,14 (8) :706-716.

同被引文献11

  • 1Hu Y, Ouyang W, Wu F, et al. Enhanced radiosensitivity of SW480 cells via TRAIL up-regulation mediated by EGR1 promoter [J]. Oncol Rep, 2009, 29(4): 765 -771.
  • 2Meirovitz A, Hernaano E, Lerner I, et al. Role of heparanase in radiation-enhanced invasiveness of pancreatic carcinoma[ J ]. Cancer Res, 2011, 71 (7): 2772-2780.
  • 3Datta R, Rubin E, Sukhatma V, el al. Ionizing radiation activates transcription of the EGR1 gene via CArG elements [ J ]. Proc Nail Acad Sci, 1992, 89(21) : 10149 - 10153.
  • 4Sukhatme VP, Cao XM, Chang I,C, et al. A zinc finger-encoding gene co-regulated with c-fos during growth and differentiation, and after cellular depolarization[J]. Cell, 1988, 53(1): 37 -43.
  • 5Santiago FS, Lowe HC, Day FL, el al. Early growth response factor-I induction by injury is triggered by release and paracrine activation by fibroblast growth factor-2 [ J]. Am J Pathol, 1999,.
  • 6Datta R, Rubin E, Sukhatme V, et al. Ionizing radiation activates transcription of the EGR1 gene via CAr(; elements[ J ]. Proc Natl Acad Sci U S A, 1992, 89(21 ) : 10149 - 10153.
  • 7Brooks C, Dong Z. Regulation of mitochondrial morphological dynamics during apoptosis by Bcl-2 family proteins: a key in Bak? [J] Cell Cycle, 2007, 6(24) : 3043 -3047.
  • 8Willis SN, Fletcher JI, Kaufmann T, et al. Apoptosis initialed when BH3 ligands engage muhiple Bcl-2 homologs, not Bax or Bak[J]. Science, 2007, 315(5813): 856-859.
  • 9Borbely AA, Murvai M, Konya J. et al. Effects of human papillo- mavirus type 16 oncoproteins on survivin gene expression [ J ]. J Gen Virol, 2006, 87 (Pt2) : 28? -294.
  • 10Hori T, Kondo T, Kanamori M, et al. Ionizing radiation enhances tumor necrosis factor-related apoplosis-inducing ligand ( TRAIL)- induced apoptosis through up-regulations of death receptor 4 ( DR4 ) and death receptor5 ( DR5 ) in human osleosarcoma Orthop Res, 2010, 28(6) : 739 -745.

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