Distinct 3p21.3 deletions in lung cancer and identification of a new human semaphorin

Oncogene. 1996 Mar 21;12(6):1289-97.

Abstract

Loss of chromosome 3p is a critical event in the pathogenesis of lung cancer. Overlapping homozygous 3p21.3 deletions in lung cancer cell lines involving GNAI2 were characterized and found to involve a region of genomic instability. A new widely expressed Semaphorin, H.SemaIV, was isolated from the GNAI2 deletion region. Reduced H.SemaIV expression allowed identification of additional cell lines with submicroscopic or larger deletions of the locus which occurred in a heterogeneous manner. We also demonstrate the presence of a distinct 3p21.3 homozygous deletion region, adjacent to the DNA mismatch repair gene, hMLH1, and identified deletions in direct tumors. This appears to represent one of the first demonstrations of homozygous deletions affecting 3p in direct lung tumors.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Base Sequence
  • Blotting, Northern
  • Carcinoma, Small Cell / genetics*
  • Chromosome Mapping
  • Chromosomes, Artificial, Yeast
  • Chromosomes, Human, Pair 3*
  • DNA Probes
  • DNA, Neoplasm / genetics
  • Gene Deletion*
  • Homozygote
  • Humans
  • Lung Neoplasms / genetics*
  • Molecular Sequence Data
  • Nerve Growth Factors / genetics*
  • Polymerase Chain Reaction
  • Sequence Homology, Amino Acid
  • Tumor Cells, Cultured

Substances

  • DNA Probes
  • DNA, Neoplasm
  • Nerve Growth Factors
  • semaphorin IV

Associated data

  • GENBANK/U33920
  • GENBANK/U33921