期刊文献+

血浆游离DNA定量检测在胃癌诊断中的价值

Quantitative Analysis of Plasma Cell-free DNA and Its Clinical Value in the Diagnosis of Gastric Cancer
下载PDF
导出
摘要 目的探讨血浆游离DNA定量检测在胃癌诊断中的价值。方法收集33例胃癌患者、44例健康对照者血液标本,血浆微量DNA抽提试剂盒提取血浆游离DNA,实时荧光定量PCR检测血浆游离DNA含量,评价血浆游离DNA水平在胃癌的诊断中的价值。结果胃癌组血浆游离DNA水平高于对照组(P<0.001);胃癌敏感性和特异度分别72.7%和93.2%,ROC曲线下面积为0.902。TNMⅢ期患者血浆游离DNA水平高于Ⅰ/Ⅱ期患者(P<0.05)。结论血浆游离DNA定量检测对胃癌的诊断具有一定的临床意义。 Objective To explore the cell-free DNA in the plasma of patients with gastric cancer and evaluate its diagnostic value. Methods The plasma cellfree DNA of 33 patients with gastric cancer and 44 controls were extracted and purified by TIANamp Macro DNA Kit. Quantitation of plasma DNA was performed by realtime fluores-cence quantitative PCR. ROC curve was used to evaluate the diagnostic value of plasm cell-free DNA for gastric cancer. Results The level of plasma cell-free DNA of patients was significantly higher than that of the controls. In addition,plasma cell-free DNA level was associated with TNM stage(P〈0.05). Conclusion Quantification of plasma cell-free DNA may be a valuable tool in the diagnostics of gastric cancer.
出处 《中国卫生标准管理》 2016年第1期161-162,共2页 China Health Standard Management
关键词 胃癌 血浆游离DNA 实时荧光定量PCR 诊断 Gastric cancer Plasma cell-free DNA RT-q PCR Diagnosis
  • 相关文献

参考文献7

  • 1陈万青,张思维,曾红梅,郑荣寿,邹小农,赵平,吴良有,李光琳,赫捷.中国2010年恶性肿瘤发病与死亡[J].中国肿瘤,2014,23(1):1-10. 被引量:882
  • 2Gahan PB, Swaminathan R. Circttlating nucleic acids in plasma and serum. Recent developments[ J ]. Ann N Y Acad Sci, 2008( 1137 ): 1-6.
  • 3ChoiJJ, Reich CF 3rd, Pisetsky DS. The role ofmacrophages in the in vitro generation of extracellular DNA from apoptotic and necrotic cells [J].Imnaunoloqy, 2005, 115 ( 1 ) :55-62.
  • 4Jung M, Klotzek S, Lewandowski M, et al. Changes in concentration of DNA in serum and plasma during storage of blood samples IJ ]. . Clin Chem, 2003, 49 ( 6 Pt 1 ) : 1028-1029.
  • 5张蓓,沈立松.实时荧光定量PCR的研究进展及其应用[J].国外医学(临床生物化学与检验学分册),2003,24(6):327-329. 被引量:80
  • 6Swaminathan R, Butt AN. Circulating nucleic acids in plasma and serum: recent developments[ J ]. Ann N Y Acad Sci ,2006(1075 ) 1-9.
  • 7Fleischhacker M, Schmidt B. Circulating nucleic acids ( CNAs ) and cancer- -asurvey [J]. .BiochimBiophysActa, 2007, 1775 ( 1 ) : 181-232.

二级参考文献19

  • 1Lie YS;Petropoulos CJ.Advances in quantitative PCR technology:5' nuclease assays[J],1998(01).
  • 2Giulietti A;Overbergh L;Valckx D.An overview of real-time quantitative PCR: applications to quantify cytokine gene expression,2001(04).
  • 3Heid CA;Stevens J;Livak K J.Real time quantitativePCR[J],1996(06).
  • 4Yin JL;Shackel NA;Zekry A.Real-time reverse transcriptase-polymerase chain reaction (RT-PCR) for measurement of cytokine and growth factor mRNA expression with fluorogenic probes or SYBR Green I[J],2001(03).
  • 5Tyagi S;Bratu DP;Kramer FR.Multicolor molecular beacons for allele discrimination[J],1998(01).
  • 6Whitcombe D;Theaker J;Guy SP.Detection of PCR products using self-probing amplicons and fluorescence[J],1999(08).
  • 7Nazarenko IA;Bhatnagar SK;Hohman RJ.A closed tube format for amplification and detection of DNA based on energy transfer[J],1997(12).
  • 8Wittwer CT;Herrmann MG;Moss AA.Continuous fluorescence monitoring of rapid cycle DNA amplification[J],1997(01).
  • 9Walker NJ.Real-time and quantitative PCR: applications to mechanism-based toxicology[J],2001(03).
  • 10Krauter J;Heil G;Ganser A.The AML1/MTG8 fusion transcript in t (8; 21) positive AML and its implication for the detection of minimal residual disease; malignancy,2001(05).

共引文献960

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