A non-random deletion in the p53 gene in oral squamous cell carcinoma

Br J Cancer. 1996 Jun;73(11):1381-6. doi: 10.1038/bjc.1996.262.

Abstract

In a retrospective study of the mutational spectrum of the p53 gene in oral squamous cell carcinoma, 80 primary tumours diagnosed in 1980-90 were included. Using polymerase chain reaction/single strand conformation polymorphism (PCR/SSCP) analysis 47 mutations were found distributed in 39 of the tumours (49%). Unexpectedly, the majority of the mutations (29/47; 62%) were found in exon 8, and at sequencing 17 of them showed a 14 bp deletion in codons 287-292, causing formation of a stop codon and accordingly a truncated protein lacking the C-terminal. The majority of the patients with the 14 bp deletion were women (13/17), and it seemed as though certain potential risk factors for carcinoma of the head and neck were less common in this group.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Age Factors
  • Aged
  • Base Sequence
  • Carcinogens
  • Carcinoma, Squamous Cell / epidemiology
  • Carcinoma, Squamous Cell / genetics*
  • Carcinoma, Squamous Cell / pathology
  • Codon
  • DNA Primers
  • Environmental Exposure
  • Exons
  • Female
  • Genes, p53*
  • Humans
  • Male
  • Molecular Sequence Data
  • Mouth Neoplasms / classification
  • Mouth Neoplasms / epidemiology
  • Mouth Neoplasms / genetics*
  • Mouth Neoplasms / pathology
  • Point Mutation
  • Polymerase Chain Reaction
  • Polymorphism, Single-Stranded Conformational
  • Retrospective Studies
  • Risk Factors
  • Sequence Deletion*
  • Sex Characteristics
  • Smoking

Substances

  • Carcinogens
  • Codon
  • DNA Primers