Frequent mutations in NOTCH1 ligand-binding regions in Japanese oral squamous cell carcinoma

Biochem Biophys Res Commun. 2014 Oct 3;452(4):980-5. doi: 10.1016/j.bbrc.2014.09.021. Epub 2014 Sep 16.

Abstract

Recent studies showed that head and neck squamous cell carcinoma (HNSCC) including oral squamous cell carcinoma (OSCC) of Caucasian, Chinese and Indian patients frequently have NOTCH1 mutations. We found eight of 84 OSCC in Japanese patients have point mutations (9.5%) correspond to the ligand binding region of NOTCH1 protein. Two set of them are the same mutations and all mutations are non-synonymous G>A transitions. In addition, median disease-free survival is significantly longer in patients with NOTCH1-mutated tumors as compared to those without the mutation (P<0.05). The protein structure simulation based on X-ray crystallography indicated that new p.A465T mutation leads to a conformational change of NOTCH1 ligand binding domain as well as the p.G481S mutant NOTCH1 with a loss of flexibility around this residue. These results suggest that NOTCH1 mutation occurs frequently in Japanese OSCC in the vicinity of the ligand binding region and, these mutations cause downregulation of the NOTCH1 function.

Keywords: Japanese oral squamous cell carcinoma; Ligand binding region; NOTCH1; Point mutation; Protein structure simulation.

MeSH terms

  • Aged
  • Amino Acid Substitution / genetics
  • Binding Sites / genetics
  • Carcinoma, Squamous Cell / diagnosis
  • Carcinoma, Squamous Cell / epidemiology*
  • Carcinoma, Squamous Cell / genetics*
  • Female
  • Genetic Markers / genetics
  • Genetic Predisposition to Disease / epidemiology
  • Genetic Predisposition to Disease / genetics
  • Humans
  • Japan / epidemiology
  • Male
  • Models, Molecular*
  • Mouth Neoplasms / diagnosis
  • Mouth Neoplasms / epidemiology*
  • Mouth Neoplasms / genetics*
  • Mutation / genetics
  • Polymorphism, Single Nucleotide / genetics
  • Prevalence
  • Protein Conformation
  • Receptor, Notch1 / genetics*
  • Receptor, Notch1 / ultrastructure*
  • Reproducibility of Results
  • Risk Factors
  • Sensitivity and Specificity

Substances

  • Genetic Markers
  • NOTCH1 protein, human
  • Receptor, Notch1