Heterogeneous molecular mechanisms underlie attenuated familial adenomatous polyposis

Francesca Cattaneo, Sara Molatore, Markos Mihalatos, Angela Apessos, Tiziana Venesio, Silvia Bione, Pierangela Grignani, Georgios Nasioulas, Guglielmina Nadia Ranzani

Research output: Contribution to journalArticlepeer-review

Abstract

PURPOSE: Familial adenomatous polyposis is a phenotypically heterogeneous disease predisposing to colorectal cancer. It is dominantly transmitted, when associated with the APC gene, and recessively inherited, when associated with MUTYH gene. We searched for APC and MUTYH germline alterations in Italian and Greek patients with attenuated polyposis, a phenotypic variant whose genetic cause remains unknown in many cases. METHODS: We studied 26 unrelated patients (and 16 relatives) with multiple colorectal adenomas (3-100, by endoscopic analysis) that had screened APC mutation-negative by protein truncation test. We searched for APC rearrangements by multiplex ligation-dependent probe amplification and for MUTYH mutations by sequencing. We performed a screening of five MUTYH recurrent pathogenic mutations in 501 Italian and 144 Greek controls. RESULTS: One patient proved to carry an APC whole-gene deletion; 4 of 25 (16%) patients showed biallelic and 3 of 25 (12%) monoallelic MUTYH mutations. In the three heterozygous subjects no pathogenetic variants were found in OGG1, MTH1, APE1, MSH2, and MSH6 genes. Frequency assessment of MUTYH mutations in healthy subjects showed that only Y165C and G382D reach a subpolymorphic frequency. CONCLUSION: Attenuated polyposis patients without "conventional" APC mutations are genetically heterogeneous, and the phenotype is not directly related to the germline defect. Therefore, the families' appropriate management requires an accurate genetic and clinical investigation.

Original languageEnglish
Pages (from-to)836-841
Number of pages6
JournalGenetics in Medicine
Volume9
Issue number12
DOIs
Publication statusPublished - Dec 2007

Keywords

  • Colorectal cancer
  • Germline mutations
  • Molecular mechanisms
  • Phenotype
  • Polyposis

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics

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