Filaggrin gene polymorphism associated with Epstein-Barr virus-associated tumors in China

Virus Genes. 2017 Aug;53(4):532-537. doi: 10.1007/s11262-017-1463-x. Epub 2017 Apr 28.

Abstract

Mutations of filaggrin gene (FLG) have been identified as the cause of ichthyosis vulgaris, while recently FLG mutations were found to be associated with gastric cancer. This study aimed to investigate the association of filaggrin polymorphism with Epstein-Barr virus-associated tumors in China. A total of 200 patients with three types of tumors and 117 normal control samples were genotyped at three common FLG mutation loci (rs3126085, K4671X, R501X) by using Sequenom MassARRAY technique. The χ 2 test was used to evaluate the relationship between the mutation and the three kinds of tumors. A two-sided P value of <0.05 was considered statistically significant. The results showed that two single-nucleotide polymorphism (SNP) loci (rs3126085, K4671X) were significantly associated with nasopharyngeal carcinoma in genetic model. In addition, the two SNPs K4671X and rs3126085 were related to Epstein-Barr virus (EBV)-associated gastric carcinoma (EBVaGC) and EBV-negative gastric carcinoma (EBVnGC), respectively. Furthermore, allele distributions in EBVaGC and EBVnGC were verified to be different in both SNP loci.

Keywords: Epstein–Barr virus; Filaggrin; Gastric carcinoma; Nasopharyngeal carcinoma; SNP.

MeSH terms

  • Adult
  • Aged
  • China
  • Epstein-Barr Virus Infections / genetics*
  • Epstein-Barr Virus Infections / metabolism
  • Epstein-Barr Virus Infections / virology
  • Female
  • Filaggrin Proteins
  • Genotype
  • Herpesvirus 4, Human / genetics
  • Herpesvirus 4, Human / physiology*
  • Humans
  • Intermediate Filament Proteins / genetics*
  • Intermediate Filament Proteins / metabolism
  • Male
  • Middle Aged
  • Mutation
  • Polymorphism, Single Nucleotide*
  • Stomach Neoplasms / genetics*
  • Stomach Neoplasms / metabolism
  • Stomach Neoplasms / virology

Substances

  • FLG protein, human
  • Filaggrin Proteins
  • Intermediate Filament Proteins