p53-mutant clones and field effects in Barrett's esophagus

Cancer Res. 1999 Oct 1;59(19):4784-7.

Abstract

Previous studies have demonstrated multifocal neoplasia in Barrett's esophagus. We evaluated 213 mapped, flow-purified, endoscopic biopsies to determine the distribution of p53-mutant clones in the Barrett's segments of 58 patients who had high-grade dysplasia without cancer. Twenty-nine patients (50%) had p53 mutations in their Barrett's segments, including 3 patients with multiple distinct p53 mutations. p53-mutant clones, including diploid cell populations, underwent expansion from 1 to 9 cm in the Barrett's segment. In 12 of 29 patients (41%) with a p53 mutation, the same mutation was found at every evaluated level of the metaplastic epithelium. This extensive p53-mutant clonal expansion suggests a somatic genetic basis for previous observations of field effects in Barrett's esophagus.

Publication types

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

MeSH terms

  • Adenocarcinoma / genetics*
  • Adenocarcinoma / pathology
  • Amino Acid Substitution
  • Barrett Esophagus / complications
  • Barrett Esophagus / genetics*
  • Barrett Esophagus / pathology
  • Cloning, Molecular
  • Esophageal Neoplasms / genetics*
  • Esophageal Neoplasms / pathology
  • Frameshift Mutation
  • Genes, p53*
  • Humans
  • Mutation*
  • Point Mutation
  • Polymerase Chain Reaction
  • Sequence Deletion
  • Tumor Suppressor Protein p53 / chemistry
  • Tumor Suppressor Protein p53 / genetics*

Substances

  • Tumor Suppressor Protein p53