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循环TA和CEA mRNA指标诊断消化系统恶性肿瘤血液转移 被引量:1

STUDY ON THE VALUE OF DETECTING TAAND CEA MRNAFOR DIAGNOSING HEMATOGENOUS METASTASIS OF DIGESTIVE SYSTEM MALIGNANTTUMOR
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摘要 目的:探讨检测血液中端粒酶活性(TA)和癌胚抗原信使核糖核酸(CEA mRNA)诊断消化系统恶性肿瘤血液转移的应用价值。方法:选择123例消化系统恶性肿瘤患者(肿瘤组,其中肿瘤转移患者64例、未发现转移的患者59例)和124例非肿瘤性消化道疾病患者(对照组)为对象,应用端粒末端重复序列扩增-杂交-酶联免疫检测技术检测TA、逆转录-套式-聚合酶链反应技术检测CEA mRNA。结栗:肿瘤组TANCEA mRNA阳性率明显高于对照组(P<0.01),肿瘤转移组TANCEA mRNA阳性率明显高于未转移组(P<0.01),TA和CEA mRNA诊断消化系统肿瘤血液转移的特异性、敏感性、阳性预测值、阴性预测值分别为88.1%和91.5%、79.7%和89.1%、87.90/0和91.9%、80.0%和88.5%。结论:检测血液标本中TA和CEA mRNA对诊断消化系统恶性肿瘤血液转移具有较高的应用价值。 Objective:To investigate the value of detecting telomerase activity (TA) and Carcinoembryonic antigen mRNA (CEA mRNA) for diagnosing hematogenous metastasis of digestive system malignant tumor. Methods: 123 digestive system malignant tumor patients (tumor group that includes 64 metastasis patients and 59 non-metasta- sis patients) and 124 non-tumor digestive system diseases patients (non-tumor group) were used in this study;TRAP- Hyb-ELISA and RT-NP-PCR were respectively used to detect TA and CEA mRNA.Results:The TA and CEA mRNA positive rate of tumor group were obviously higher than that of non-tumor group (P 〈 0.01) ;The TA and CEA mRNA positive rate of metastasis patients were significantly higher than that of non-metastasis patients (P 〈 0.01).The specificity, sensitivity, positive predictive value and negative predictive value of TA and CEA mRNA in diagnosing of hematogenous metastasis of digestive system cancer were 88.1% and 91.5%,79.7% and 89.1%,87.9% and 91.9%, 80.0% and 88.5% respectively.Conclusions:Decting TA and CEA mRNA in blood has higher applying value in diagnosing hematogenons metastasis of digestive system malignant tumor.
出处 《承德医学院学报》 2007年第4期361-363,共3页 Journal of Chengde Medical University
关键词 血液 端粒酶活性 癌胚抗原信使核糖核酸 消化系统恶性肿瘤 血液转移 Blood TA CEA mRNA Digestive system malignant tumor Hematogenous metastasis
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  • 1[1]Blackburn E H, Gall J G. J Mol Biol, 1978; 120: 33-35.
  • 2[2]Flint J, Bates G P, Clark K, et al. Nat Genet, 1997;15: 252-257.
  • 3[3]Klobutcher L A, Swanton M T, Donini P, et al. Proc Natl Acad Sci USA, 1981; 78: 3015-3019.
  • 4[4]Gravel S, Larrivee M, Labrecque P, et al. Science,1998; 280: 741-744.
  • 5[5]van Steensel B, Smogorzewka A, de Lange T. Cell,1998; 92: 401-413.
  • 6[6]Griffith J .D, Comeau L, Rosenfield S, et al. Cell,1999; 97: 503-514.
  • 7[7]Carol W G. Cell, 1999; 97: 419-422.
  • 8[8]Nugent C, Hughes T R, Lue N F, et al. Science, 1996;274: 249-252.
  • 9[9]Shore D. Biol Chem, 1997; 378: 591-597.
  • 10[10]Marcand S, Gilson E, Shore D, et al. Science, 1997;275: 986-990.

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