DPC4 gene mutation in colitis associated neoplasia

Gut. 1997 Jan;40(1):120-2. doi: 10.1136/gut.40.1.120.

Abstract

Background: Colitis associated dysplasia and cancer often have deletions involving the long arm of chromosome 18q, suggesting the location of a tumour suppressor gene critical for their tumorigenesis. The DPC4 gene, which is genetically inactivated in pancreatic and other cancers, has recently been described.

Aim: Because DPC4 is located at 18q21.1, the hypothesis that it could be a mutated tumour suppressor gene in colitis associated neoplasms was tested.

Patients: Advanced neoplastic lesions from six patients having chronic colitis were analysed for DPC4.

Methods: Individual exons of DPC4 were amplified by the polymerase chain reaction (PCR) and sequenced from genomic DNA of tissue specimens dissected by cryostat.

Results: DPC4 was found to have biallelic inactivation in one of three neoplasms shown to have allelic loss of 18q. The mutation had been acquired somatically in a plaque of high grade dysplasia. The mutation created a non-sense codon, which would cause premature termination of protein translation.

Conclusion: The DPC4 gene is a target of 18q LOH events in colitis associated neoplasia.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Aged
  • Base Sequence
  • Chromosome Deletion
  • Chromosomes, Human, Pair 18 / genetics*
  • Colitis, Ulcerative / complications
  • Colitis, Ulcerative / genetics*
  • Colorectal Neoplasms / etiology
  • Colorectal Neoplasms / genetics*
  • Crohn Disease / complications
  • Crohn Disease / genetics*
  • Exons
  • Genes, Tumor Suppressor / genetics*
  • Heterozygote
  • Humans
  • Middle Aged
  • Molecular Sequence Data
  • Mutation*
  • Oncogenes
  • Polymerase Chain Reaction