Clinical and molecular analysis of hereditary non-polyposis colorectal cancer in Chinese colorectal cancer patients

被引:7
|
作者
Wang, Jun
Luo, Mao-Hong
Zhang, Zuo-Xing
Zhang, Pei-Da
Jiang, Xi-Li
Ma, Dong-Wang
Suo, Rong-Zeng
Zhao, Li-Zhong
Qi, Qing-Hui
机构
[1] Hereditary Colorectal Tumors Registry, Tianjin 300022, Peoples R China
[2] Tianjin Med Univ, Tianjin 300022, Peoples R China
[3] Tianjin Bijiang Hosp, Tianjin 300022, Peoples R China
关键词
hereditary non-polyposis colorectal cancer; colorectal cancer; mismatch repair gene; immunohistochemistry; microsatellite instability;
D O I
10.3748/wjg.v13.i10.1612
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To analyze the frequency of hereditary non-polyposis colorectal cancer (HNPCC) in Chinese colorectal cancer (CRC) patients, and to discuss the value of microsatellite instability (MSI) and/or immunohistochemistry (IHC) for MSH2/MLH1 protein analysis as pre-screening tests in China. METHODS: The Amsterdam criteria I and II (clinical diagnosis) and/or germline hMLH1/hMSH2 mutations (genetic diagnosis) were used to classify HNPCC families. Genetic tests, including microsatellite instability, immunohistochemistry for MSH2/MLH1 proteins and hMSH2/hMLH1 genes, were performed in each proband. RESULTS: From July 2000 to June 2004, 1988 patients with colorectal cancer were analysed and 114 CRC patients (5.7%) from 48 families were categorized as having HNPCC, including 76 from 26 families diagnosed clinically and 38 from the other 22 families diagnosed genetically. The sensitivity and specificity of high MSI and IHC for predicting mutations were 100% and 54%, and 79% and 77%, respectively. CONCLUSION: The frequency of HNPCC is approximately 10% among all Chinese CRC cases. The MSI and IHC detections for hMSH2/hMLH1 proteins are reliable prescreening tests for hMLH1/hMSH2 germline mutations in families suspected of having HNPCC. (c) 2007 The WJG Press. All rights reserved.
引用
收藏
页码:1612 / 1617
页数:6
相关论文
共 50 条
  • [31] Frequency of incomplete hereditary non-polyposis colorectal cancer
    Sahm, SW
    Raedle, J
    MuellerHardt, M
    Esser, N
    Caspary, WF
    Zeuzem, S
    GASTROENTEROLOGY, 1997, 112 (04) : A649 - A649
  • [32] Hereditary non-polyposis colorectal cancer: an updated review
    Anwar, S
    Hall, C
    White, J
    Deakin, M
    Farrell, W
    Elder, JB
    EUROPEAN JOURNAL OF SURGICAL ONCOLOGY, 2000, 26 (07): : 635 - 645
  • [33] Hereditary non-polyposis colorectal cancer: pathogenesis and mechanisms
    Rozen, P
    EXOGENOUS FACTORS IN COLONIC CARCINOGENESIS, 2003, 128 : 55 - 68
  • [34] Descriptive epidemiology of hereditary non-polyposis colorectal cancer
    deLeon, MP
    TUMORI, 1996, 82 (02) : 102 - 106
  • [35] Strategies for screening for hereditary non-polyposis colorectal cancer
    Loukola, A
    de la Chapelle, A
    Aaltonen, LA
    JOURNAL OF MEDICAL GENETICS, 1999, 36 (11) : 819 - 822
  • [36] Clinical aspects and management of hereditary non-polyposis colorectal cancer (HNPCC)
    Bertario, L
    Aste, H
    Arrigoni, A
    Fracasso, P
    Rossini, FR
    Rossetti, C
    Valanzano, R
    TUMORI, 1996, 82 (02) : 117 - 121
  • [37] Clinical characteristics of Taiwanese hereditary non-polyposis colorectal cancer kindreds
    Wei, SC
    Wang, MH
    Shieh, MC
    Wang, CY
    Wong, JM
    JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION, 2002, 101 (03) : 206 - 209
  • [38] Patient identification and clinical management in hereditary non-polyposis colorectal cancer
    Al-Taie, O
    EXOGENOUS FACTORS IN COLONIC CARCINOGENESIS, 2003, 128 : 92 - 100
  • [39] Testing guidelines for hereditary non-polyposis colorectal cancer
    Asad Umar
    John I. Risinger
    Ernest T. Hawk
    J. Carl Barrett
    Nature Reviews Cancer, 2004, 4 : 153 - 158
  • [40] Genetic counseling in hereditary non-polyposis colorectal cancer
    Heouaine, A
    Mareni, C
    Varesco, L
    Genuardi, M
    Neri, G
    TUMORI, 1996, 82 (02) : 136 - 142