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微卫星不稳定检测在新疆地区人群HNPCC家系筛查中的应用 被引量:1

Application of microsatellite instability examination for the screening of hereditary nonpolyposis colorectal cancer pedigree in Xinjiang area
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摘要 目的通过微卫星不稳定性(MSI)检测在中国新疆地区人群遗传性非息肉病性结直肠癌(HNPCC)家系筛查,为临床筛查提供相关依据。方法通过聚合酶链反应-单链构象多态性(PCR-SSCP)技术对新疆地区的HNPCC家系组(A组12例)、可疑HNPCC家系组(B组10例)及散发型大肠癌(C组20例)进行检测及分析。结果 HNPCC家系、可疑HNPCC家系组及散发型大肠癌高度微卫星不稳定(MSI-H)情况分别为83.3%、50.0%、10.0%,HNPCC家系、可疑HNPCC家系组分别较散发型大肠癌高度微卫星不稳定情况高(P<0.05),差异有统计学意义。结论 MSI与HNPCC情况高度相关,作为HNPCC筛查的重要手段,对指导临床有重要意义。 Objective To use microsatellite instability (MSI) examination to test hereditary nonpolyposis colorectal cancer (HNPCC) pedigree in Xinjiang area in order to provides related basis for clinical screening. Methods PCR - SSCP was conducted in HNPCC pedigree ( group A, 12 cases), the suspicious HNPCC pedigree ( group B, 10 cases) and the sporadic colorectal cancer cases ( group C, 20 cases) in Xin- jiang area. The results were analyzed. Results The percentages of MSI - H were 83.3 %, 50.0% and 10% in group A, group B and group C respectively. There was significant difference between group A and group C, and between group B and group C ( P 〈 0.05 ). Conclusion MSI and HNPCC is highly related. MSI identification therefore is of clinical importance for guiding the screening of HNPCC .
出处 《临床和实验医学杂志》 2012年第22期1763-1765,共3页 Journal of Clinical and Experimental Medicine
基金 新疆哈萨克家族性HNPCC微卫星不稳定和错配修复基因突变规律研究国家自然基金81060035 新疆人群HNPCC家系筛查及微卫星不稳定和错配修复基因突变规律研究博士资金2010JC17
关键词 非息肉病性结直肠癌 DNA错配修复 微卫星不稳定 Hereditary nonpolyposis colorectal cancer DNA mismatch repair Microsatellite instability
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  • 1盛剑秋,田素丽,吕扬,陈香宇,李世荣.遗传性非息肉病性结直肠癌的微卫星不稳定研究[J].胃肠病学和肝病学杂志,2004,13(5):537-539. 被引量:7
  • 2[1]Lynch HT,de la Chapelle A.Hereditary colorectal cancer.N Engl J Med 2003; 348:919-932
  • 3[2]de la Chapelle A.Genetic predisposition to colorectal cancer.Nat Rev Cancer 2004; 4:769-780
  • 4[3]Vasen HF,Mecklin JP,Khan PM,Lynch HT.The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC).Dis Colon Rectum 1991; 34:424-425
  • 5[4]Vasen HF,Watson P,Mecklin JP,Lynch HT.New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC,Lynch syndrome) proposed by the International Collaborative group on HNPCC.Gastroenterology 1999; 116:1453-1456
  • 6[5]Rodriguez-Bigas MA,Boland CR,Hamilton SR,Henson DE,Jass JR,Khan PM,Lynch H,Perucho M,Smyrk T,Sobin L,Srivastava S.A National Cancer Institute Workshop on Hereditary Nonpolyposis Colorectal Cancer Syndrome:meeting highlights and Bethesda guidelines.J Natl Cancer Inst 1997; 89:1758-1762
  • 7[6]Peltomaki P,Vasen H.Mutations associated with HNPCC predisposition-Update of ICG-HNPCC/INSiGHT mutation database.Dis Markers 2004; 20:269-276
  • 8[7]Nakagawa H,Hampel H,de la Chapelle A.Identification and characterization of genomic rearrangements of MSH2 and MLH1 in Lynch syndrome (HNPCC) by novel techniques.Hum Mutat 2003; 22:258
  • 9[8]Taylor CF,Charlton RS,Butn J,Sheridan E,Taylor GR.Genomic deletions in MSH2 of MLH1 are a frequent cause of hereditary non-polyposis colorectal cancer:identification of novel and recurrent deletions by MLPA.Hum Mutat 2003; 22:428-433
  • 10[9]Nystrom-Lahti M,Kristo P,NicolAldes NC,Chang SY,Aaltonen LA,Moisio Al Jarvinen HJ,Mecklin JP,Kinzler KW,Vogelstein B.Four ng mutations and Alu-mediated recombination in hered ry colon cancer.Nat Med 1995; 1:1203-1206

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