Mutations of the K-ras and p53 genes in gastric adenocarcinomas from a high-incidence region around Florence, Italy

Cancer Res. 1995 Jun 15;55(12):2665-72.

Abstract

K-ras and p53 gene mutations in intestinal-type gastric carcinomas from a high-incidence area around Florence, Italy, were studied by single strand conformation polymorphism and DNA sequencing analysis. Single-strand conformation polymorphism analysis of K-ras indicated aberrant bands in 13 of 34 cases. Sequencing revealed point mutations in 7 (including two at a previously unreported site in codon 11), a significantly higher frequency than reported in countries other than Japan. No K-ras mutations were identified in stage III tumors. Single-strand conformation polymorphisms in p53 exons 5-8 occurred in 30 of 34 cases, with mutations identifiable by direct sequencing in 65% of the cases. Of these, 91% were base substitutions, a value similar to that usually reported, but the percentage of G:C to A:T transitions (90% in this study, 89% in all published European cases combined) differed significantly from that in Oriental cases (48%). The percentage of A:T to G:C transitions was greater in Oriental (22%) than European cases (2%), as was also true for transversions (30% in Oriental tumors, 9% in European tumors). The frequency of mutations at CpG sites (14%) varied significantly from the 67% in cases from a neighboring region in Italy. Helicobacter pylori infection was established in 19 cases and was somewhat more common in cases lacking a p53 mutation.

Publication types

  • Comparative Study

MeSH terms

  • Adenocarcinoma / epidemiology*
  • Adenocarcinoma / genetics*
  • Adenocarcinoma / pathology
  • Alleles
  • Base Sequence
  • DNA Primers
  • DNA, Neoplasm / analysis
  • Europa
  • Exons
  • Genes, p53*
  • Genes, ras*
  • Geography
  • Helicobacter Infections / diagnosis
  • Helicobacter Infections / epidemiology
  • Helicobacter pylori / isolation & purification
  • Humans
  • Immunohistochemistry
  • Incidence
  • Italy / epidemiology
  • Japan / epidemiology
  • Molecular Sequence Data
  • Mutation*
  • Neoplasm Staging
  • Point Mutation
  • Polymerase Chain Reaction
  • Polymorphism, Genetic
  • Stomach Neoplasms / epidemiology*
  • Stomach Neoplasms / genetics*
  • Stomach Neoplasms / pathology
  • Tumor Suppressor Protein p53 / analysis
  • Tumor Suppressor Protein p53 / biosynthesis

Substances

  • DNA Primers
  • DNA, Neoplasm
  • Tumor Suppressor Protein p53