MBD4 mutations are rare in gastric carcinomas with microsatellite instability

M Pinto, Y Wu, G Suriano, RGJ Mensink, A Duval, C Oliveira, B Carvalho, R Hamelin, R Seruca, RMW Hofstra*

*Corresponding author for this work

    Research output: Contribution to journalArticleAcademicpeer-review

    19 Citations (Scopus)


    MBD4 encodes a protein that interacts with the mismatch repair protein hMLH1. Therefore. it has been postulated that mutations in MBD4 may result in mismatch repair deficiency. Furthermore, it was shown that MBD4 is a target gene in mismatch repair-deficient tumors. We searched for mutations of MBD4 in sporadic gastric carcinomas (SGC) and compared them with the MSI status of the tumors by screening a series of 42 SGC [22 high microsatellte instability (MSI-H) and 20 microsatellite stable (MSS)] for mutations in both the poly(A)10 and (A)6 tracts of the gene as well as in its entire coding sequence. Mutations of the poly(A) 10 tract of MBD4 were also screened in 126 MSI-H colon carcinomas. One of the 22 MSI-H gastric carcinomas and 12 of 126 MSI-H colon carcinomas showed MBD4 mutations in the poly(A)10 tract of exon 3. In addition, seven sequence variants were found in SGC, all of them having a polymorphic nature. We conclude that MBD4 mutations in the entire coding sequence, including the two poly(A) tracts, are rare in MSI gastric carcinomas. MBD4 is likely to be a bystander target gene in MSI-H tumors. (C) 2003 Elsevier Inc. All rights reserved.

    Original languageEnglish
    Pages (from-to)103-107
    Number of pages5
    JournalCancer Genetics and Cytogenetics
    Issue number2
    Publication statusPublished - Sept-2003


    • DNA
    • GENE
    • CANCER
    • MED1

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