Search for mutations and examination of allelic expression imbalance of the p73 gene at 1p36.33 in human lung cancers

Cancer Res. 1998 Apr 1;58(7):1380-3.

Abstract

We examined 61 lung cancer cases to determine whether alterations of p73, a novel monoallelically expressed p53-like molecule, may be involved in the pathogenesis of lung cancer. Allelic loss at the p73 locus at 1p36.33 was observed in 42% (11 of 26 informative cases), and squamous cell carcinoma tended to carry this lesion most frequently. Somatic mutations in the p73 gene itself, however, were not detected, despite our extensive search. We found interindividual difference in the allelic expression of p73 in normal lung, as well as intertissue variance, even within the same individual, but preferential loss of the expressed allele appeared to be an unlikely mechanism for p73 inactivation. This study, consequently, suggests the presence of an as yet unidentified tumor suppressor gene or genes within the subtelomeric region of 1p, warranting further studies aimed at its isolation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles*
  • Carcinoma, Non-Small-Cell Lung / genetics
  • Carcinoma, Squamous Cell / genetics
  • Chromosomes, Human, Pair 1*
  • DNA-Binding Proteins / genetics*
  • Gene Deletion*
  • Genes, Tumor Suppressor*
  • Humans
  • Lung Neoplasms / genetics*
  • Mutation*
  • Nuclear Proteins / genetics*
  • Polymerase Chain Reaction
  • Polymorphism, Single-Stranded Conformational
  • Tumor Protein p73
  • Tumor Suppressor Proteins

Substances

  • DNA-Binding Proteins
  • Nuclear Proteins
  • TP73 protein, human
  • Tumor Protein p73
  • Tumor Suppressor Proteins