EGFR exon 19 in-frame deletion and polymorphisms of DNA repair genes in never-smoking female lung adenocarcinoma patients
Journal
International Journal of Cancer
Journal Volume
132
Journal Issue
2
Pages
449-458
Date Issued
2013
Author(s)
Yang S.-Y.
Yang T.-Y.
Li Y.-J.
Chen K.-C.
Liao K.-M.
Hsu K.-H.
Tsai C.-R.
Chen C.-Y.
Hsu C.-P.
Hsia J.-Y.
Chuang C.-Y.
Tsai Y.-H.
Huang M.-S.
Su W.-C.
Chen Y.-M.
Hsiung C.A.
Shen C.-Y.
Chang G.-C.
Chen C.-J.
Abstract
We explored potential associations between genetic polymorphisms in genes related to DNA repair and detoxification metabolism and epidermal growth factor receptor (EGFR) mutations in a cohort of 410 never-smoking patients with lung adenocarcinoma. Multivariate-adjusted odds ratios (aORs) and corresponding 95% confidence intervals (CI) of EGFR mutation status in association with the genotypes of DNA repair and detoxification metabolism genes were evaluated using logistic regression analysis. We found an association between in-frame deletion in EGFR exon 19 and a single nucleotide polymorphism (SNP) rs1800566C/T located in NQO1 (aOR, 2.2 with 95% CI, 1.0-4.8) in female never-smokers. The SNP rs744154C/G in ERCC4 was also associated with the EGFR exon 19 in-frame deletion both in never-smokers (aOR, 1.7 with 95% CI, 1.0-3.0) and female never-smokers (aOR, 1.9 with 95% CI, 1.0-3.6). Although the association was marginally significant in multivariate logistic regression analysis, the A/A genotype of rs1047840 in EXO1 was associated with a 7.6-fold increase in the occurrence of the EGFR exon 19 in-frame deletion in female never-smokers. Moreover, risk alleles in NQO1, ERCC4 and EXO1 were associated with an increasing aOR of the EGFR exon 19 in-frame deletion both in never-smokers (p = 0.007 for trend) and female never-smokers (p = 0.002 for trend). Our findings suggest that the in-frame deletion in EGFR exon 19 is associated with polymorphisms in DNA repair and detoxification metabolism genes in never-smoking lung adenocarcinoma patients, especially in females. Copyright ? 2012 UICC.
SDGs
Other Subjects
8 oxoguanine DNA n glycosylase 1; cytochrome P450 1A1; epidermal growth factor receptor; excision repair cross complementing protein 4; exonuclease 1; protein; protein MSH2; reduced nicotinamide adenine dinucleotide (phosphate) dehydrogenase (quinone); unclassified drug; XRCC1 protein; adult; aged; allele; article; cancer patient; cohort analysis; confidence interval; detoxification; DNA repair; exon; female; gene deletion; genotype; human; logistic regression analysis; lung adenocarcinoma; major clinical study; male; multivariate analysis; multivariate logistic regression analysis; priority journal; risk assessment; single nucleotide polymorphism; smoking; Adenocarcinoma; Adult; Aged; Aged, 80 and over; Alleles; DNA Mutational Analysis; DNA Repair; DNA Repair Enzymes; DNA-Binding Proteins; Exodeoxyribonucleases; Exons; Female; Genetic Association Studies; Humans; Logistic Models; Lung Neoplasms; Male; Middle Aged; MutS Homolog 2 Protein; NAD(P)H Dehydrogenase (Quinone); Polymorphism, Genetic; Polymorphism, Single Nucleotide; Receptor, Epidermal Growth Factor; Sequence Deletion; Sex Factors; Smoking
Type
journal article