Immunohistochemistry and microsatellite instability testing for selecting MLH1, MSH2 and MSH6 mutation carriers in hereditary non-polyposis colorectal cancer

  • Authors:
    • Trinidad Caldés
    • Javier Godino
    • Ana Sanchez
    • Cesar Corbacho
    • Miguel De la Hoya
    • Jose Lopez Asenjo
    • Carmen Saez
    • Julian Sanz
    • Manuel Benito
    • Santiago Ramon Y Cajal
    • Eduardo Diaz-Rubio
  • View Affiliations

  • Published online on: Wednesday, September 1, 2004
  • Pages: 621-629
  • DOI: 10.3892/or.12.3.621

Abstract

Hereditary non-polyposis colorectal cancer (HNPCC) represents 1-3% of all colorectal cancers. HNPCC is caused by a constitutional defect in a mismatch repair (MMR) gene, most commonly affecting the genes MLH1, MSH2 and MSH6. The MMR defect results in an increased cancer risk, with the greatest lifetime risk for colorectal cancer and other cancers associated to HNPCC. The HNPCC-associated tumor phenotype is generally characterized by microsatellite instability (MSI) and immunohistochemical loss of expression of the affected MMR protein. The aim of this study was to determine the sensitivity of IHC for MLH1, MSH2 and MSH6, and MSI analysis in tumors from known MMR gene mutation carriers. Fifty-eight paired normal and tumor samples from HNPCC families enrolled in our high-risk colorectal cancer registry were studied for the presence of germline mutations in MLH1, MSH2 and MSH6 by DGGE and direct sequencing. MSI analysis and immunostaining for MLH1, MSH2 and MSH6 were evaluated. Of the 28 patients with a real pathogenic mutation, loss of immunohistochemical expression for at least 1 of these MMR proteins was found, and all except 1 have MSI-H. Sensitivity by MSI analysis was 96%. IHC analysis had a sensitivity of 100% in detecting MMR deficiency in carriers of a pathogenic MMR mutation, and can be used to predict which gene is expected to harbor the mutation for MLH1, MSH2 and MSH6. This study suggests that both analyses are useful for selecting high-risk patients because most MLH1, MSH2 and MSH6 gene carriers will be detected by this 2-step approach. This practical method should have immediate application in the clinical work of patients with inherited colorectal cancer syndromes.
Journal Cover

September 2004
Volume 12 Issue 3

Print ISSN: 1021-335X
Online ISSN:1791-2431

2013 Impact Factor: 2.191
Ranked #33/202 Oncology
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APA
Caldés, T., Godino, J., Sanchez, A., Corbacho, C., De la Hoya, M., Lopez Asenjo, J., Saez, C., Sanz, J., Benito, M., Ramon Y Cajal, S., & Diaz-Rubio, E. (2004). Immunohistochemistry and microsatellite instability testing for selecting MLH1, MSH2 and MSH6 mutation carriers in hereditary non-polyposis colorectal cancer. Oncology Reports, 12(3), 621-629.
MLA
Caldés, Godino, Sanchez, Corbacho, De la Hoya, Lopez Asenjo, Saez, Sanz, Benito, Ramon Y Cajal, and Eduardo Diaz-Rubio. "Immunohistochemistry and microsatellite instability testing for selecting MLH1, MSH2 and MSH6 mutation carriers in hereditary non-polyposis colorectal cancer." Oncology Reports Oncology Reports 12.3 (2004): 621-629.
Chicago
Caldés, Godino, Sanchez, Corbacho, De la Hoya, Lopez Asenjo, Saez, Sanz, Benito, Ramon Y Cajal, and Eduardo Diaz-Rubio. "Immunohistochemistry and microsatellite instability testing for selecting MLH1, MSH2 and MSH6 mutation carriers in hereditary non-polyposis colorectal cancer." Oncology Reports Oncology Reports 12 no. 3 (2004): 621-629.