Alterations of Fas (Apo-1/CD95) gene in non-small cell lung cancer

Oncogene. 1999 Jun 24;18(25):3754-60. doi: 10.1038/sj.onc.1202769.


Fas (Apo-1/CD95) is a cell-surface receptor involved in cell death signaling. The key role of the Fas system in negative growth regulation has been studied mostly within the immune system, and somatic mutations of Fas gene in cancer patients have been described solely in lymphoid-lineage malignancies. However, many non-lymphoid tumor cells have been found to be resistant to Fas-mediated apoptosis, which suggests that Fas mutations, one of the possible mechanisms for Fas-resistance, may be involved in the pathogenesis of non-lymphoid malignancies as well. In this study, we have analysed the entire coding region and all splice sites of the Fas gene for the detection of the gene mutations in 65 human non-small cell lung cancers by polymerase chain reaction, single strand conformation polymorphism and DNA sequencing. Overall, five tumors (7.7%) were found to have the Fas mutations, which were all missense mutations. Four of the five mutations identified were located in the cytoplasmic region (death domain) known to be involved in the transduction of an apoptotic signal and one mutation was located in the transmembrane domain. This is the first report on the Fas gene mutations in non-lymphoid malignancies, and the data presented here suggests that alterations of the Fas gene might lead to the loss of its apoptotic function and contribute to the pathogenesis of some human lung cancers.

Publication types

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

MeSH terms

  • Adenocarcinoma / genetics
  • Apoptosis / genetics
  • Carcinoma, Non-Small-Cell Lung / genetics*
  • Carcinoma, Squamous Cell / genetics
  • DNA Mutational Analysis
  • DNA, Neoplasm / genetics
  • Fas Ligand Protein
  • Gene Deletion
  • Humans
  • Lung Neoplasms / genetics*
  • Membrane Glycoproteins / biosynthesis
  • Membrane Glycoproteins / genetics
  • Mutation
  • Neoplasm Proteins / biosynthesis
  • Neoplasm Proteins / genetics*
  • Polymerase Chain Reaction
  • Polymorphism, Single-Stranded Conformational
  • RNA Splicing
  • fas Receptor / biosynthesis
  • fas Receptor / genetics*


  • DNA, Neoplasm
  • FASLG protein, human
  • Fas Ligand Protein
  • Membrane Glycoproteins
  • Neoplasm Proteins
  • fas Receptor