Literature DB >> 15831908

Association between family history and mismatch repair in colorectal cancer.

R P Coggins1, L Cawkwell, S M Bell, G P Crockford, P Quirke, P J Finan, D T Bishop.   

Abstract

BACKGROUND AND AIMS: Germline mutations in mismatch repair (MMR) genes cause a greatly increased risk of cancer of the gastrointestinal and female reproductive tracts (hereditary non-polyposis colorectal cancer (HNPCC)). Loss of MMR expression is common in colorectal cancer (CRC) overall. Such loss is assumed to be acquired predominantly, although a population of CRC cases will include individuals with unrecognised MMR mutations. This study examines the association between MMR gene expression and family history of cancer among the CRC population.
METHODS: Individuals with CRC were identified from two well characterised populations: (1) consecutive hospital patients (n = 644) and (2) a population based cases series (n = 249). CRC was examined for expression of hMLH1 and hMSH2 using immunohistochemistry, and expression was related to family history using logistic regression.
RESULTS: hMLH1 and hMSH2 expression was assessed in 732 CRCs with 8% showing loss of expression. No association was seen overall for hMLH1 or hMSH2 expression and family history of CRC. Loss of hMSH2 was predicted by family history of extracolonic cancer (odds ratio (OR) 5.78 (95% confidence interval (CI) 0.95-35.18)) and family history suggestive of HNPCC (OR 27.84 (95% CI 4.37-177.56)). Loss of hMLH1 was not predicted by family history of extracolonic cancer or a family history suggestive of HNPCC but was for a family history of at least two affected relatives (OR 4.88 (95% CI 1.25-19.03)).
CONCLUSIONS: Individuals with hMSH2 deficient CRC in the general population exhibit a family history and other characteristics suggestive of HNPCC, and may carry germline MMR mutations. Loss of hMLH1 is only associated with a strong family history of extracolonic cancer at older ages, suggesting a novel mechanism of susceptibility.

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Year:  2005        PMID: 15831908      PMCID: PMC1774492          DOI: 10.1136/gut.2003.017517

Source DB:  PubMed          Journal:  Gut        ISSN: 0017-5749            Impact factor:   23.059


  39 in total

1.  Germ-line mutation of the hMSH6/GTBP gene in an atypical hereditary nonpolyposis colorectal cancer kindred.

Authors:  Y Akiyama; H Sato; T Yamada; H Nagasaki; A Tsuchiya; R Abe; Y Yuasa
Journal:  Cancer Res       Date:  1997-09-15       Impact factor: 12.701

2.  Choice of management strategy for colorectal cancer based on a diagnostic immunohistochemical test for defective mismatch repair.

Authors:  L Cawkwell; S Gray; H Murgatroyd; F Sutherland; L Haine; M Longfellow; S O'Loughlin; D Cross; O Kronborg; C Fenger; N Mapstone; M Dixon; P Quirke
Journal:  Gut       Date:  1999-09       Impact factor: 23.059

3.  A population-based study of endometrial cancer and familial risk in younger women. Cancer and Steroid Hormone Study Group.

Authors:  S B Gruber; W D Thompson
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  1996-06       Impact factor: 4.254

4.  After hMSH2 and hMLH1--what next? Analysis of three-generational, population-based, early-onset colorectal cancer families.

Authors:  Mark A Jenkins; Laura Baglietto; Gillian S Dite; Damien J Jolley; Melissa C Southey; Jonathan Whitty; Leeanne J Mead; D James B St John; Finlay A Macrae; D Timothy Bishop; Deon J Venter; Graham G Giles; John L Hopper
Journal:  Int J Cancer       Date:  2002-11-10       Impact factor: 7.396

5.  Hereditary susceptibility to colorectal cancer. Relatives of early onset cases are particularly at risk.

Authors:  N R Hall; D T Bishop; B M Stephenson; P J Finan
Journal:  Dis Colon Rectum       Date:  1996-07       Impact factor: 4.585

6.  Frequent loss of hMLH1 by promoter hypermethylation leads to microsatellite instability in adenomatous polyps of patients with a single first-degree member affected by colon cancer.

Authors:  Luigi Ricciardiello; Ajay Goel; Vilma Mantovani; Tania Fiorini; Stefania Fossi; Dong K Chang; Veronica Lunedei; Paolo Pozzato; Rocco M Zagari; Luca De Luca; Lorenzo Fuccio; Giuseppe N Martinelli; Enrico Roda; C Richard Boland; Franco Bazzoli
Journal:  Cancer Res       Date:  2003-02-15       Impact factor: 12.701

7.  Hypermethylation of the hMLH1 promoter in colon cancer with microsatellite instability.

Authors:  J M Cunningham; E R Christensen; D J Tester; C Y Kim; P C Roche; L J Burgart; S N Thibodeau
Journal:  Cancer Res       Date:  1998-08-01       Impact factor: 12.701

8.  Replication errors in benign and malignant tumors from hereditary nonpolyposis colorectal cancer patients.

Authors:  L A Aaltonen; P Peltomäki; J P Mecklin; H Järvinen; J R Jass; J S Green; H T Lynch; P Watson; G Tallqvist; M Juhola
Journal:  Cancer Res       Date:  1994-04-01       Impact factor: 12.701

9.  Frequency of hereditary nonpolyposis colorectal cancer. A prospective multicenter study in Finland.

Authors:  J P Mecklin; H J Järvinen; A Hakkiluoto; H Hallikas; K M Hiltunen; N Härkönen; I Kellokumpu; S Laitinen; J Ovaska; J Tulikoura
Journal:  Dis Colon Rectum       Date:  1995-06       Impact factor: 4.585

10.  Microsatellite instability in human colonic cancer is not a useful clinical indicator of familial colorectal cancer.

Authors:  W S Samowitz; M L Slattery; R A Kerber
Journal:  Gastroenterology       Date:  1995-12       Impact factor: 22.682

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  4 in total

1.  Mismatch repair protein expression and colorectal cancer in Hispanics from Puerto Rico.

Authors:  Wilfredo E De Jesus-Monge; Carmen Gonzalez-Keelan; Ronghua Zhao; Stanley R Hamilton; Miguel Rodriguez-Bigas; Marcia Cruz-Correa
Journal:  Fam Cancer       Date:  2010-06       Impact factor: 2.375

2.  Genetic variants in XRCC2: new insights into colorectal cancer tumorigenesis.

Authors:  Karen Curtin; Wei-Yu Lin; Rina George; Mark Katory; Jennifer Shorto; Lisa A Cannon-Albright; Gillian Smith; D Timothy Bishop; Angela Cox; Nicola J Camp
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2009-08-18       Impact factor: 4.254

3.  Prevalence of pathological germline mutations of hMLH1 and hMSH2 genes in colorectal cancer.

Authors:  Dandan Li; Fulan Hu; Fan Wang; Binbin Cui; Xinshu Dong; Wencui Zhang; Chunqing Lin; Xia Li; Da Wang; Yashuang Zhao
Journal:  PLoS One       Date:  2013-03-19       Impact factor: 3.240

4.  A novel heterozygous germline deletion in MSH2 gene in a five generation Chinese family with Lynch syndrome.

Authors:  Bin Wu; Wuyang Ji; Shengran Liang; Chao Ling; Yan You; Lai Xu; Min-Er Zhong; Yi Xiao; Hui-Zhong Qiu; Jun-Yang Lu; Santasree Banerjee
Journal:  Oncotarget       Date:  2017-07-14
  4 in total

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