Role of FHIT in human cancer

J Clin Oncol. 1999 May;17(5):1618-24. doi: 10.1200/JCO.1999.17.5.1618.

Abstract

Through investigation of hemizygous and homozygous deletions in common human cancers, including lung cancer, we have cloned and characterized a gene at chromosome region 3p14.2, FHIT, that is inactivated in epithelial tumors, particularly in tumors resulting from exposure to environmental carcinogens. In some tumors, particularly those associated with environmental carcinogens, alterations in the FHIT gene occur quite early in the development of cancer. In other cancers, Fhit inactivation seems to be a later event, possibly associated with progression to more aggressive neoplasias. Thus, detection of Fhit expression by immunohistochemistry in premalignant and malignant tissues may provide important diagnostic and prognostic information.

MeSH terms

  • Acid Anhydride Hydrolases*
  • Animals
  • Carcinoma, Non-Small-Cell Lung / genetics
  • Chromosome Fragility
  • Chromosome Mapping
  • Chromosomes, Human, Pair 1 / genetics
  • Chromosomes, Human, Pair 3 / genetics*
  • Drosophila melanogaster / genetics
  • Genes, Tumor Suppressor
  • Humans
  • Loss of Heterozygosity*
  • Lung Neoplasms / genetics
  • Neoplasm Proteins / genetics*
  • Neoplasm Proteins / metabolism
  • Precancerous Conditions / genetics*
  • Proteins / genetics*
  • Proteins / metabolism
  • Recombinant Fusion Proteins / genetics

Substances

  • Neoplasm Proteins
  • Proteins
  • Recombinant Fusion Proteins
  • fragile histidine triad protein
  • Acid Anhydride Hydrolases