Alterations of p16/CDKN2, p53 and ras genes in oral squamous cell carcinomas and premalignant lesions

J Oral Pathol Med. 1996 May;25(5):232-8. doi: 10.1111/j.1600-0714.1996.tb01377.x.

Abstract

Exons 1-3 of the p16/CDKN2 gene, exons 4-9 of the p53 gene and exons 1 and 2 of H-, K- and N-ras genes were screened for mutations by a combination of immunohistochemistry and single-strand conformational polymorphism (SSCP) analyses of polymerase chain reaction products from human surgical samples of both frank oral squamous cell carcinomas and premalignant lesions. The samples included 20 squamous cell carcinomas, 10 epithelial dysplasias and 10 epithelial hyperplasias. No identifiable gene mutations were detected in any of the dysplasias or hyperplasias, while 2 (10%) deletions and 2 (10%) mutations of p16/CDKN2, along with 5 (25%) p53 mutations were found in the advanced carcinomas, yielding characteristic p16/ CDKN2 and p53 changes. A mutation in the K-ras gene was found in single carcinoma and dysplastic samples. From the data, it can be argued that p16/CDKN2 and p53 mutations are relatively late occurrences in human oral tumorigenesis and that genetic alterations of the ras genes may not play a significant role in squamous neoplasia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carcinoma, Squamous Cell / genetics*
  • Carcinoma, Squamous Cell / pathology
  • Carrier Proteins / genetics*
  • Cyclin-Dependent Kinase Inhibitor p16
  • DNA Primers
  • Enzyme Inhibitors*
  • Epithelium / pathology
  • Exons / genetics
  • Gene Deletion
  • Genes, Tumor Suppressor / genetics*
  • Genes, p53 / genetics*
  • Genes, ras / genetics*
  • Humans
  • Hyperplasia
  • Immunohistochemistry
  • Mouth Neoplasms / genetics*
  • Mouth Neoplasms / pathology
  • Mutation / genetics
  • Polymerase Chain Reaction
  • Polymorphism, Single-Stranded Conformational
  • Precancerous Conditions / genetics*
  • Precancerous Conditions / pathology
  • Protein Kinase Inhibitors*
  • Protein Kinases / genetics

Substances

  • Carrier Proteins
  • Cyclin-Dependent Kinase Inhibitor p16
  • DNA Primers
  • Enzyme Inhibitors
  • Protein Kinase Inhibitors
  • Protein Kinases