The genetic polymorphisms of HER-2 and the risk of lung cancer in a Korean population

BMC Cancer. 2008 Dec 4:8:359. doi: 10.1186/1471-2407-8-359.

Abstract

Background: Human Epidermal Growth Factor Receptor 2 (HER-2; also known as erbB-2 or neu), a proto-oncogene of the receptor tyrosine kinase superfamily, has been associated with carcinogenesis and prognosis of human cancers, acting as a binding partner of other epidermal growth factor receptor (EGFR) family in the activation of EGFR signaling. Amplification of the HER-2 gene has been reported in lung cancer, where it has been associated with poor prognosis. In this study, we investigated whether the four polymorphisms (-3444C>T, -1985 G>T, I655A A>G and P1170A C>G) of the HER-2 gene are associated with the risk of lung cancer in Korean populations.

Methods: The frequencies of 4 polymorphisms of the HER-2 gene were examined by the polymerase chain reaction-restriction fragment length polymorphism or the single-nucleotide polymorphism-identification technology assay in the 407 lung cancer patients and 407 healthy controls.

Results: The frequencies of the 4 polymorphisms were not significantly different between patient and control groups in overall subjects. However, in the subgroup analysis, the 3 single nucleotide polymorphisms (-3444C>T, -1985G>T and P1170A C>G) showed statistically significant differences in the subgroups of females, non-smokers, and non-drinkers (p < 0.05). Additionally, we found the association between the risk of lung cancer and the polymorphisms of HER-2 gene in non-smoker subgroups with adenocarcinoma (p < 0.05).

Conclusion: Our results suggest that the polymorphisms of the HER-2 gene are associated with an increased susceptibility to lung cancer in females, non-smokers and non-drinkers subgroups in the Korean population.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alcohol Drinking / epidemiology
  • Female
  • Genotype
  • Humans
  • Korea / epidemiology
  • Lung Neoplasms / epidemiology*
  • Lung Neoplasms / genetics*
  • Male
  • Polymorphism, Genetic / genetics*
  • Proto-Oncogene Mas
  • Receptor, ErbB-2 / genetics*
  • Risk Factors
  • Smoking / epidemiology

Substances

  • MAS1 protein, human
  • Proto-Oncogene Mas
  • ERBB2 protein, human
  • Receptor, ErbB-2