期刊文献+

尿液DD3mRNA定量检测在前列腺癌诊断中的价值 被引量:2

DD3 mRNA Analysis in Urine for the Diagnosis of Prostate Cancer
下载PDF
导出
摘要 目的探讨前列腺按摩后尿沉渣中DD3mRNA含量在前列腺癌诊断中应用价值。方法收集前列腺癌(Pca)患者18例、良性前列腺增生(BPH)33例,在前列腺穿刺活检前收集前列腺按摩后的尿液,离心取细胞沉淀物,用荧光实时定量RT- PCR方法检测DD3 mRNA和PSAmRNA含量,以PSAmRNA作为管家基因校正尿沉渣中的前列腺细胞,以DD3mRNA/PSAmR- NA比值表示尿DD3mRNA含量。用ROC曲线对DD3mRNA诊断PCa的性能进行分析,并与血清tPSA进行了比较,同时探讨了尿DD3mRNA阳性率与临床分期和病理分级的关系。结果Pca患者尿DD3mRNA表达量明显高于BPH患者,差异具有统计学意义(P【0.05)。ROC曲线分析结果显示,ROC-AUC=0.716(95%CI:0.572~0.861)。当截断值为0.118时,DD3mRNA的灵敏性、特异性、准确性、阳性预测值、阴性预测值、阳性似然比、阴性似然比分别为67.0%、78.8%、77.4%、63. 2%、83.9%、3.41和0.35。若血清tPSA分别以4ng/ml和10ng/ml为截断值时,灵敏度分别为100%和94.4%,特异度分别为15.25和57.6%。DD3mRNA的阳性率与临床分期和病理分级无关。结论DD3mRNA的特异性明显高于血清PSA,尿液DD3mRNA的检测可减少不必要的前列腺穿刺,作为PCa的一种非损伤性诊断方法具有良好的应用前景。 Objective To study the clinical utility of DD3mRNA expression in urine after prostate massage.Methods DD3mRNA was detected by a real-time fluorescent quantitative reverse transcription polymerase chain reaction(FQ-RT-PCR)based on Taqman technique in Urine samples of 33 BPH and 18 PCa patient after prostate massage.PSA was used as a housekeeping gene to normalize the number of prostate cell,and then DD3mRNA/PSAmRNA ratio was used as a diagnostic tool for the accurate identification of pros- tate cancer cells and to compare the DD3mRNA expression in urinary sediment between BPH and Pca patients.The ROC curve was used to evaluate the diagnostic efficacy of DD3mRNA in urine samples and compared with serum tPSA.DD3mRNA expression among different clinic pathological parameters was analysed.Results There was significant difference of DD3mRNA expression in urinary sediment between BPH and Pca patients(P<0.05).The AUC-ROC was 0.716(95% CI:0.572~0.861)at cutoff 0.118.The sen- sitivity,specificity,accuracy,positive predictive value,negative predictive value,positive likelihood ratio and negative likelihood ratio for DD3mRNA were 67.0%,78.8%,77.4%,63.2%,83.9%,94.3%,3.41 and 0.35,respectively.The sensitivity was 100% and 94.4% and the specificity was 15.2% and 57.6% at serum tPSA cutoff value 4ng/ml and 10ng/ml,respectively.There was no sig- nificant difference between DD3mRNA positive rate and clinic pathological parameters.Conclusion DD3mRNA expression had ex- cellent diagnose efficacy for proatate cancer as a non-invasive method and its specificity is superior to serum tPSA.
出处 《浙江检验医学》 2006年第2期3-6,共4页 Zhejiang Journal of Laboratory Medicine
基金 浙江省自然科学基金(SZJO2003)
关键词 DD3基因 实时荧光定量RT-PCR 前列腺癌 尿液 DD3 gene mRNA Real-time quantitative RT-PCR Prostate cancer
  • 相关文献

参考文献1

二级参考文献2

共引文献11

同被引文献36

  • 1姚宏.前列腺癌p504s标记物研究最新进展[J].山西医药杂志,2004,33(8):635-636. 被引量:5
  • 2艾金霞 ,于秀艳 ,王雪松 .血清hK2 ELISA方法的建立及在前列腺癌诊断中的应用[J].北华大学学报(自然科学版),2005,6(2):125-128. 被引量:4
  • 3Kinoshita Y, Kuratsukuri K, Landas S, et al.Expression of prostate-specific membrane antigen in normal and malignant human tissues[J]. World J Surg, 2006,30(4) :628.
  • 4Zhang L,Ji G, Li X, et al.fPSMtPSA ratio optimize the early diagnosis is in the prostate cancer[J].Chin J Andro,l 2004,10(8): 582.
  • 5Jemal A ,Siege R ,Ward E, et al.Cancer statistics[J].2008 CA Cancer J Clin 2008 58(2):71.
  • 6Luo J,Zha S,Gage WR,et al.α-M ethylacyl-CoA racemase a new molecular marker for prostate cancer[J].Cancer Res, 2002,62(8):2220.
  • 7Jiang Z,W oda BA,Rock KL,et al.P504S a new molecular marker fou the detdction of prostate carcinoma [J].Am J Surg Pathol,2001, 25(11) : 1397.
  • 8Zhou M ,Chinnaiyan AM ,Kleer CG ,et al.Alpha-methylacyl-CoA racemase: a novel tumormarker overexpressed in several human cancers and their precursor lesions[J].Am J Surg Patho1,2006,26(7) :926.
  • 9Murphy GP,Elgamal AA,Su SL,et al.Current evaluation of the tissue localization and diagnostic utility of prostate specific membrane antigen[J].Cancer, 1998,83(11) :2259.
  • 10Kularatne SA,Wang K,Santhapuram HK,et al.Prostatespecific membrane antigen targeted imaging and therapy of prostate cancerusing a PSMA inhibitor as a homin ligand[J].Mol-Pharm, 2009,6(3) :780.

引证文献2

二级引证文献7

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