期刊文献+

辐射诱导Gadd45基因表达作为生物剂量计的实验室评估 被引量:1

Evaluation of the feasibility with Gadd45 as a radiation biodosimeter
下载PDF
导出
摘要 为了考察电离辐照后人外周血中Gadd45基因表达的个体差异,评价Gadd45作为基因表达辐射生物剂量计的实用性,采集了27个健康人外周血进行60Co照射,提取白细胞mRNA,以β-actin作为内对照基因,建立了相对标准曲线法实时定量聚合酶链式反应(Polymerase chain reaction,PCR)方法,并以此方法探索辐照后Gadd45表达的剂量-效应关系。结果表明,0~2.5Gy剂量范围内,Gadd45的mRNA表达水平随照射剂量增加而上调,通过拟合建立了0~2.5Gy剂量范围内,Gadd45/β-actin相对表达量与照射剂量间的剂量-效应直线方程(y=0.216+0.258x,p<0.001,R2=0.650)。发现Gadd45 mRNA表达水平在个体间存在一定差异,应用该剂量-效应直线方程,可以对0~2.5Gy照射剂量范围内的血液照射剂量作相对估算。 To survey the variance of Gadd45 mRNA in different people's blood exposured to ionizing radiation, which is necessary in evaluating the feasibility of Gadd45 as a radiation biodosimeter, 27 normal persons' peripheral blood was irradiated with ^60Co γ-rays in vitro. And its RNA was isolated from white cell. The relative real-time quantitative PCR by standard curve method was set up using β-actin as internal standards. With this method, Gadd45 mRNA expression change was observed after ionizing radiation. It has been found that in 0-2.5Gy range the rela- tionship between the ratio of Gadd45 mRNA / β-actin and irradiation dose represents certain line correlation. A linear regression equation (y=0.216+0.258x, p〈0.001, R^2=0.650) has been obtained using statistics regression analysis method which can be used to estimate the biological doses involved in radiation accidents though the variance of the Gadd45 mRNA level among different people is marked.
出处 《辐射研究与辐射工艺学报》 CAS CSCD 北大核心 2008年第3期129-133,共5页 Journal of Radiation Research and Radiation Processing
基金 国家自然科学基金(30606109)资助
关键词 电离辐射生物剂量计 外周血白细胞 GADD45 荧光实时定量聚合酶链式反应 Ionizing radiation biodosimeter, Peripheral blood leucocyte, Gadd45, Fluorescence real-time quantitative polymerase chain reaction (PCR)
  • 相关文献

参考文献13

二级参考文献76

  • 1徐丽昕,蒋本荣,艾辉胜.GADD45基因——一种可能的新的生物剂量计[J].军事医学科学院院刊,2004,28(5):479-481. 被引量:3
  • 2徐顺高,黄新祥,周丽萍.荧光实时定量RT-PCR观察伤寒杆菌鞭毛z66和d/j抗原基因表达方法的建立[J].江苏大学学报(医学版),2005,15(1):21-24. 被引量:3
  • 3Bustin S A. Absolute quantification of mRNA using real-time reverse transcription polymerase chain reaction assays. J Mol Endocrinol, 2000, 25 (2): 169~193.
  • 4Giulietti A, Overbergh L, Valckx D, et al. An overview of real-time quantitative PCR: applications to quantify cytokine gene expression.Methods, 2001, 25 (4): 386~401.
  • 5Livak K J, Schmittgen T D. Analysis of relative gene expression data using real-time quantitative PCR and the 2 (-Delta Delta C (T))Method. Methods, 2001, 25 (4): 402~408.
  • 6Liu W, Saint D A. A new quantitative method of real time reverse transcription polymerase chain reaction assay based on simulation of polymerase chain reaction kinetics. Anal Biochem, 2002, 302 (1):52~59.
  • 7Easton DF,Ford D,Bisnop DT.Breast and ovarian cancer incidence in BRCA1-mutation carriers.Breast Cancer Linkage Consortium [J].AmJ HumGenet,1995,56:265-271.
  • 8Ford D and Easton DF.The genetics of breast and ovarian cancer[J].BrJ Cancer,1995,72:805-812.
  • 9Miki Y,Swensen J,Shattuck Eidens D,et al.A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1 [J].Science,1994,266:66-71.
  • 10Deng CX,Brodie SG.Roles of BRCA1 and its interacting proteins [J].Bioessays,2000,22(8):728-737.

共引文献156

同被引文献15

  • 1黄越承,蔡建明,韩玲,高福,崔建国,高建国.γ射线诱发的小鼠淋巴细胞白血病中MDM_2的表达研究(英文)[J].第二军医大学学报,2004,25(6):598-602. 被引量:2
  • 2徐丽昕,艾辉胜,蒋本荣,姚波,余长林,郭梅,黄雅静,孙琪云.电离辐射对人外周血淋巴细胞GADD45基因表达的影响[J].辐射研究与辐射工艺学报,2006,24(2):111-114. 被引量:17
  • 3Levine AJ, Oren M. The first 30 years of p53: growing ever more complex[J]. Nat Rev Cancer,2009,9 (10) :749 - 758.
  • 4Zak-Prelich M, Norval M, Venner TJ, et al. cis-Urocanic acid does not induce the expression of immunosuppressive cytokines in murine keratinocytes [ J ]. Photochem Photobio1,2001,73 ( 3 ) :238 - 244.
  • 5Cheng L, Spitz MR, Hong WK, et al. Reduced expression levels of nucleotide excision repair genes in lung cancer: a case-control analysis [J]. Carcinogenesis ,2000,21 ( 8 ) : 1527 - 1530.
  • 6刘树铮.医学放射生物学[M].北京:原子能出版社,2009:292-309.
  • 7Abbas T, Dutta A. p21 in Cancer: intricate networks and multiple activities [J]. Nat Rev Cancer,2009,9 ( 6 ) :400 - 414.
  • 8Takeuchi S, Takahashi A, Motoi N, et al. Intrinsic cooperation between p16INK4a and p21 wata/cip1 in the onset of cellular senescence and tumor suppression in vivo[J]. Cancer Res,2010,70(22) :9381 - 9390.
  • 9Cole AM, Ridgway RA, Derkits SE, et al. p21 loss blocks senes- cence following Apc loss and provokes tumourigenesis in the renal but not the intestinal epithelium [ J ]. EMBO Mol Med, 2010,2 ( ll ) : 472 - 486.
  • 10George RJ, Sturmoski MA, May R, et aL Loss of p21Waf1/Cip1/Sdil en- hances intestinal stem cell survival following radiation injury[J]. Am J Physiol Gastrointest Liver Physio1,2009,296 ( 2 ) : G245 - 254.

引证文献1

二级引证文献1

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