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人粪便SFRP2基因甲基化分析对结直肠癌的诊断价值 被引量:2

Value of SFRP2 methylation analysis in stool in early diagnosis of colorectal cancer
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摘要 目的探讨人粪便中分泌型卷曲相关蛋白2(SFRP2)基因甲基化分析用于结直肠癌(CRC)早期诊断的可行性。方法从87例结直肠癌或良性病变的患者及24例正常对照者的粪便中分别提取DNA,采用甲基化特异性PCR(MSP)技术分析其SFRP2基因甲基化状态。结果CRC、腺瘤、增生性息肉和溃疡性结肠炎患者的SFRP2基因甲基化阳性率分别为94.2%(49/52)、52.4%(11/21)、37.5%(3/8)和16.7%(1/6)。1例正常对照SFRP2基因甲基化检测阳性。检测SFRP2基因甲基化诊断CRC及癌前病变的敏感性和特异性分别为90.5%和85.4%。结论SFRP2基因甲基化是CRC进展过程中的早期事件。粪便SFRP2基因甲基化分析可望成为CRC早期无创诊断或CRC高风险人群筛查的新途径。 [Objective] To evaluate the possibility of methylation analysis of secreted frlzzled-related protein gene 2(SFRP2)in feces for screening early colorectal cancer (CRC). [Methods] DNA was isolated from fecal samples from 87 patients with malignant or benign eolorectal diseases (52 with cancer, 21 with adenomas,8 with hyperplastic polyp and 6 with ulcerative colitis) and 24 normal volunteer, and the methylation status of SFRP2 was analyzed with methylation-specific polymerase chain reaction(MSP). [Results] Methylated SFRP2 occurred in 94.2%(49/52),52. 4%(11/21),37. 5%(3/8)and 16.7%(1/6) of patients with CRC, adenomas, hyperplstic polyps and ulcerative colitis, respectively. One normal control also revealed SFRP2 methylation. The sensitivity and specificity of SFRP2 methylation assay for CRC and precancerous lesions was 90.5% and 85.4%, respectively. [Conclusions] Hypermethylation of SFRP2 is an event that occurs early in disease progression of CRC. Analysis of fecal SFRP2 methylation is expected to serve as a new early detection way for CRC or a new screening tool for individuals at high-risk of developing colorectal neoplasm.
作者 程之红
出处 《山东医药》 CAS 北大核心 2007年第6期10-12,共3页 Shandong Medical Journal
基金 江苏省无锡市科技局科研项目(CS055010)
关键词 结肠肿瘤 直肠肿瘤 诊断 甲基化 粪便 colorectal neoplasms rectal neoplasms diagnosis methylation feces
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  • 1Kondo Y,Issa JP.Epigenetic changes in colorectal cancer[J].Cancer and Metastasis Reviews,2004,23(1-2):29-39.
  • 2Suzuki H,Watkins DN,Jair KW,et al.Epigenetic inactivation of SFRP genes allows constitutive WNT signaling in colorectal cancer[J].Nat Genet,2004,36(4):417-422.
  • 3Herman JG,Graff JR,Myohanen S,et a1.Methylation-specific PCR:a novel PCR assay for methylation status of CpG islands[J].Proc Natl Acad Sci USA,1996,93(18):9821-9826.
  • 4Zou H,Molina JR,Harrington JJ,et al.Aberrant methylation of secreted frizzled-related protein genes in esophageal adenocarcinoma and Barrett's esophagus[J].Int J Cancer,2005,116(4):584-591.
  • 5Belshaw NJ,Elliott GO,Williams EA,et al.Use of DNA from human stools to detect aberrant CpG island methylation of genes implicated in colorectal cancer[J].Cancer Epidemiol Biomarkers Prev,2004,13(9):1495-1501.
  • 6Müller HM,Oberwalder M,Fiegl H,et al.Methylation changes in faecal DNA:a marker for colorectal cancer screening[J].Lancet,2004,363(9417):1283-1285.
  • 7Lenhard K,Bommer GT,Asutay S,et al.Analysis of promoter methylation in stool:a novel method for the detection of colorectal cancer[J].Clin Gastroenterol Hepatol,2005,3(2):142-149.
  • 8Wynter CV,Kambara T,Walsh MD,et al.DNA methylation patterns in adenomas from FAP,multiple adenoma and sporadic colorectal carcinoma patients[J].Int J Cancer,2006,118(4):907-915.

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