检验医学 ›› 2014, Vol. 29 ›› Issue (7): 712-717.DOI: 10.3969/j.issn.1673-8640.2014.07.005

• 临床应用研究·论著 • 上一篇    下一篇

血清TFPI-2基因甲基化在胃癌诊断中的临床价值

朱立岳1,关明2,康志华2,高建萍3,翁丽贞1,章励1,胡雷光1   

  1. 1.上海市静安区中心医院/复旦大学华山医院静安分院检验科,上海 200040;
    2.复旦大学附属华山医院检验医学科,上海 200040;
    3.上海市静安区中心医院复旦大学华山医院静安分院消化科,上海 200040
  • 收稿日期:2014-02-18 出版日期:2014-07-30 发布日期:2014-07-21
  • 通讯作者: 胡雷光,联系电话:021-62893581。
  • 作者简介:朱立岳,男,1979年生,学士,主管技师,主要从事生物化学及分子生物学检验。
  • 基金资助:

    上海市静安区卫生系统“十、百、千”人才建设工程,专业技术骨干培养资助项目(201006B002)

Clinical significance on the detection of serum methylated tissue factor pathway inhibitor 2 gene in the diagnosis of gastric cancer

ZHU Liyue1,GUAN Ming2,KANG Zhihua2,GAO Jianping3,WENG Lizhen1,ZHANG Li1,HU Leiguang1   

  1. 1.Department of Clinical Laboratory, Shanghai Jing′ an District Central Hospital/Jing′ an Branch of Huashan Hospital, Fudan University, Shanghai 200040, China;
    2. Department of Laboratory Medicine, Huashan Hospital, Fudan University, Shanghai 200040, China;
    3.Department of Digestion, Shanghai Jing′ an District Central Hospital/Jing′ an Branch of Huashan Hospital, Fudan University, Shanghai 200040, China
  • Received:2014-02-18 Online:2014-07-30 Published:2014-07-21

摘要:

目的 通过测定组织及血清组织因子途径抑制物2(TFPI-2)基因甲基化,探讨其作为一种肿瘤标志物对胃癌诊断的临床价值。方法 收集32例胃癌、29例萎缩性胃炎作为研究对象,以30例不排除浅表性胃炎的正常对象作为对照。应用甲基化特异性聚合酶链反应(MSP)方法,测定组织及血清TFPI-2基因甲基化状态。应用电化学发光免疫法测定癌胚抗原(CEA)、糖类抗原199(CA199)。结果 组织TFPI-2基因甲基化检出率胃癌组为53.13%、萎缩性胃炎组为37.93%、对照组为3.33%。胃癌组明显高于对照组(P0.05)。血清TFPI-2基因甲基化检出率胃癌组为28.13%,萎缩性胃炎组为6.90%,对照组未检出。胃癌组明显高于萎缩性胃炎组(P0.05)和对照组(P<0.05)。血清TFPI-2基因甲基化检测灵敏度为28.13%,特异性为96.61%。血清检出阳性占组织检出阳性的比率为37.93%。胃癌组血清TFPI-2基因甲基化与性别、年龄、Borrmann′s 分期、CEACA199检测结果无关(P0.05)。胃癌组血清TFPI-2基因甲基化与CEACA199阳性检出率分别为28.13%21.88%18.75%。联合3项阳性检出率为53.13%,显著高于3项各自单独检测(P<;0.05)。结论 血清TFPI-2基因甲基化来源于组织,其对胃癌诊断特异性较高,但灵敏度较差。联合检测血清CEACA199有利于提高其灵敏度。血清TFPI-2基因甲基化测定对胃癌的诊断有一定价值。

关键词: 组织因子途径抑制物-2基因, 甲基化, 血清游离DNA, 胃癌

Abstract:

Objective Through the detection of serum and tissue methylated tissue factor pathway inhibitor 2TFPI-2 gene to investigate its clinical significance as a tumor marker for the diagnosis of gastric cancer. Methods A total of 32 gastric cancer patients and 29 atrophic gastritis patients were enrolled and 32 healthy subjects including superficial gastritis were enrolled as control group. Methylated TFPI-2 gene was detected by methylation-specific polymerase chain reactionMSP. Carcinoembryonic antigenCEA and carbohydrate antigen 199CA199 were determined by electrochemiluminescence  immunoassay. Results The positive rates of methylated TFPI-2 gene in tissue were 53.13% in gastric cancer group 37.93% in atrophic gastritis group and 3.33% in control group. Tissue methylated TFPI-2 gene was significantly higher in gastric cancer group than in control groupP0.05. The positive rates of methylated TFPI-2 gene in serum were 28.13% in gastric cancer group 6.90% in atrophic gastritis group but none in control group. Serum methylated TFPI-2 gene was significantly higher in gastric cancer group than in atrophic gastritis groupP0.05 and in control groupP0.05. The sensitivity and specificity of serum methylated TFPI-2 gene for the diagnosis of gastric cancer were 28.13% and 96.61%. The 37.93% positive rate was got in serum against tissue. The TFPI-2 gene methylation in serum showed no correlation with sex age Borrmann′ s classification CEA and CA199 in gastric cancer groupP0.05. In gastric cancer group the positive rates of methylated TFPI-2 gene CEA and CA199 were 28.13% 21.88% and 18.75% respectively. If performing the combined determination of all the 3 parameters the positive rate was 53.13% and the positive rate was significantly higher than those of the single determinationsP0.05. Conclusions The TFPI-2 gene methylation in serum derives from gastric cancer tissues and it shows high specificity for the diagnosis of gastric cancer but the sensitivity is relatively low. It can improve the sensitivity if performing the combined determination with CEA and CA199. The detection of serum TFPI-2 gene methylation has certain significance for diagnosing gastric cancer.

Key words: Tissue factor pathway inhibitor 2 gene, Methylation, Serum free DNA, Gastric cancer

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