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Familial Cancer

, Volume 5, Issue 2, pp 179–189 | Cite as

Germline Mutations of the hMLH1 and hMSH2 Mismatch Repair Genes in Belgian Hereditary Nonpolyposis Colon Cancer (HNPCC) Patients

  • M. SpaepenEmail author
  • B. Vankeirsbilck
  • S. Van  Opstal
  • S. Tejpar
  • E. Van  Cutsem
  • K. Geboes
  • E. Legius
  • G. Matthijs
Article

Abstract

Background: Hereditary nonpolyposis colon cancer (HNPCC-Lynch syndrome) is caused by mutations in genes involved in DNA mismatch repair (MMR), mostly in the hMLH1 and hMSH2 genes. The mutation spectrum in the Belgian population is still poorly documented. Aim: To report our experience on the mutation screening in Belgian familial colorectal cancer (CRC) patients, including the investigation of the pathogenicity of the missense and splice mutations. To increase the mutation detection rate by selecting the target population. Methods: Two hundred and twenty five Belgian patients with familial clustering of CRC were genetically tested. Point mutations in the hMLH1 and hMSH2 genes were screened by denaturing gradient gel electrophoresis (DGGE) followed by direct sequencing. Genomic deletions and duplications were assessed by multiplex ligase dependent probe amplification (MLPA) and multiplex PCR. Missense mutations were examined for pathogenicity by means of cosegregation of the mutation with the disease, microsatellite instability (MSI) in tumors, immunohistochemical staining of tumors and determination of the population frequency of the particular mutation. Results: Twenty five pathogenic mutations were identified from which 16 were novel: 7 frameshifts, one in frame deletion, 5 genomic deletions, 5 splice defects, 4 nonsense (stop) mutations and 3 missense mutations which were classified as pathogenic (out of 10 missense mutations). In retrospect, a mutation detection rate of 71% was obtained if MSI was used as a supplementary selection criterion in addition to familial clustering. Conclusion: Different types of pathogenic mutations in the hMLH1 and hMSH2 genes were identified in a Belgian CRC group with familial clustering. The mutation detection yield drastically increased by preliminar selection of those familial CRC patients with a microsatellite instable tumor. Considerable attention went to the assessment of the pathogenicity of the missense mutations. In practice, the cosegregation with the disease was the most relevant criterion.

Key words

hereditary nonpolyposis colon cancer (HNPCC) hMSH2 hMLH1 microsatellite instability (MSI) mismatch repair (MMR) 

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Copyright information

© Springer 2006

Authors and Affiliations

  • M. Spaepen
    • 1
    • 4
    Email author
  • B. Vankeirsbilck
    • 1
  • S. Van  Opstal
    • 1
  • S. Tejpar
    • 1
    • 2
  • E. Van  Cutsem
    • 2
  • K. Geboes
    • 3
  • E. Legius
    • 1
  • G. Matthijs
    • 1
  1. 1.Center for Human GeneticsUniversity Hospital of LeuvenLeuvenBelgium
  2. 2.Department of GastroenterologyUniversity Hospital of LeuvenLeuvenBelgium
  3. 3.Department of Pathological Anatomy of LeuvenUniversity Hospital of LeuvenLeuvenBelgium
  4. 4.Center for Human GeneticsUniversity of LeuvenLeuvenBelgium

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