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Genetic predisposition to lung adenocarcinoma among never-smoking Chinese with different epidermal growth factor receptor mutation status.

Publication ,  Journal Article
Han, L; Lee, C-K; Pang, H; Chan, H-T; Lo, I-L; Lam, S-K; Cheong, T-H; Ho, JC-M
Published in: Lung Cancer
December 2017

OBJECTIVES: The inconsistent findings from genetic association studies may be related to the heterogeneity in different molecular subtypes of lung cancer. This study evaluated the predisposing single-nucleotide polymorphisms (SNPs) in epidermal growth factor receptor (EGFR) mutant and EGFR wild-type lung adenocarcinoma separately among never-smokers. MATERIALS AND METHODS: This was a two-stage case-control study. Never-smokers with pathologically confirmed lung adenocarcinoma and healthy controls were recruited in Hong Kong and Macau. Genomic DNA was extracted and genotyped by MassARRAY. In the discovery stage, 51 SNPs were investigated at the SNP, gene and pathway level among 103 EGFR mutant and 78 EGFR wild-type lung adenocarcinoma cases compared with matched controls. In the validation stage, SNPs that were identified with significant lung cancer risk were replicated in a separate cohort of 84 lung adenocarcinoma cases and compared with 103 Chinese Han, Beijing and 105 Chinese Han, Southern public controls from the 1000 genome database. RESULTS AND CONCLUSION: The genetic association of IL-6 rs2069840 with EGFR mutant lung adenocarcinoma was ascertained. In the discovery stage, haplotype GGG in three SNPs (rs2069840, rs2069852, rs2066992) of IL-6, synergetic effects of IL-6 rs2069840 and environmental tobacco smoke in the workplace were found to be related to EGFR mutant lung adenocarcinoma. ERCC2 rs238406 showed a marginally significant association with EGFR mutant lung adenocarcinoma in the validation stage (P=0.096). ERCC2 rs50871 and ATM rs611646 showed significant association with EGFR wild-type lung adenocarcinoma in the discovery stage. In conclusion, IL-6 rs2069840 conferred susceptibility to EGFR mutant lung adenocarcinoma in a Hong Kong and Macau never-smoking Chinese population.

Duke Scholars

Published In

Lung Cancer

DOI

EISSN

1872-8332

Publication Date

December 2017

Volume

114

Start / End Page

79 / 89

Location

Ireland

Related Subject Headings

  • Smoking
  • Risk Factors
  • Polymorphism, Single Nucleotide
  • Oncology & Carcinogenesis
  • Mutation
  • Middle Aged
  • Male
  • Lung Neoplasms
  • Interleukin-6
  • Humans
 

Citation

APA
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ICMJE
MLA
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Han, L., Lee, C.-K., Pang, H., Chan, H.-T., Lo, I.-L., Lam, S.-K., … Ho, J.-M. (2017). Genetic predisposition to lung adenocarcinoma among never-smoking Chinese with different epidermal growth factor receptor mutation status. Lung Cancer, 114, 79–89. https://doi.org/10.1016/j.lungcan.2017.10.012
Han, Li, Cheuk-Kwong Lee, Herbert Pang, Hong-Tou Chan, Iek-Long Lo, Sze-Kwan Lam, Tak-Hong Cheong, and James Chung-Man Ho. “Genetic predisposition to lung adenocarcinoma among never-smoking Chinese with different epidermal growth factor receptor mutation status.Lung Cancer 114 (December 2017): 79–89. https://doi.org/10.1016/j.lungcan.2017.10.012.
Han L, Lee C-K, Pang H, Chan H-T, Lo I-L, Lam S-K, et al. Genetic predisposition to lung adenocarcinoma among never-smoking Chinese with different epidermal growth factor receptor mutation status. Lung Cancer. 2017 Dec;114:79–89.
Han, Li, et al. “Genetic predisposition to lung adenocarcinoma among never-smoking Chinese with different epidermal growth factor receptor mutation status.Lung Cancer, vol. 114, Dec. 2017, pp. 79–89. Pubmed, doi:10.1016/j.lungcan.2017.10.012.
Han L, Lee C-K, Pang H, Chan H-T, Lo I-L, Lam S-K, Cheong T-H, Ho JC-M. Genetic predisposition to lung adenocarcinoma among never-smoking Chinese with different epidermal growth factor receptor mutation status. Lung Cancer. 2017 Dec;114:79–89.
Journal cover image

Published In

Lung Cancer

DOI

EISSN

1872-8332

Publication Date

December 2017

Volume

114

Start / End Page

79 / 89

Location

Ireland

Related Subject Headings

  • Smoking
  • Risk Factors
  • Polymorphism, Single Nucleotide
  • Oncology & Carcinogenesis
  • Mutation
  • Middle Aged
  • Male
  • Lung Neoplasms
  • Interleukin-6
  • Humans