科研之友
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摘要
To derive a more precise estimation of the relationship between the excision repair cross-complementing rodent repair deficiency, group 2 (ERCC2) Lys751Gln polymorphism and lung cancer risk, a meta-analysis was performed. A total of 23 studies including 8137 cases and 9824 controls were involved in this meta-analysis. Overall, significantly elevated lung cancer risk was associated with ERCC2 Gln allele when all studies were pooled into the meta-analysis (Lys/Gln versus Lys/Lys: odds ratio (OR) = 1.10, 95% confidence interval (CI) = 1.03-1.19; Gln/Gln versus Lys/Lys: OR = 1.20, 95% CI = 1.06-1.35; dominant model: OR = 1.13, 95% Cl = 1.05-1.20; and recessive model: OR = 1.15, 95% Cl = 1.03-1.29). In the subgroup analysis by ethnicity, significantly increased risk was only found for Caucasians (Gln/Gln versus Lys/Lys: OR = 1.25, 95% CI = 1.08-1.45; dominant model: OR = 1.10, 95% CI = 1.00-1.22; and recessive model: OR = 1.22, 95% CI = 1.06-1.40). When stratified by study design, statistically significantly elevated risks were found in hospital-based studies (Lys/Gln versus Lys/Lys: OR = 1.12, 95% CI = 1.03-1.22; Gln/Gln versus Lys/Lys: OR = 1.24, 95% CI = 1.06-1.44; dominant model: OR = 1.15, 95% CI = 1.06-1.24; and recessive model: OR = 1.19, 95% CI = 1.03-1.37) and population-based studies (Gln/Gln versus Lys/Lys: OR = 1.57, 95% CI = 1.12-2.20 and recessive model: OR = 1.50, 95% CI = 1.08-2.07). In the subgroup analysis whether or not the studies were matched on smoking, significantly increased risk was found not in those matched studies but in the unmatched studies (Lys/Gln versus Lys/Lys: OR = 1.11, 95% CI = 1.03-1.19; Gln/Gln versus Lys/Lys: OR = 1.22, 95% CI = 1.07-1.40; dominant model: OR = 1.13, 95% CI = 1.05-1.22; and recessive model: OR = 1.18, 95% CI = 1.04-1.33). In conclusion, this meta-analysis suggests that the ERCC2 Lys751Gln polymorphism may contribute to lung cancer susceptibility among Caucasians.
- 出版日期2010-9
- 单位复旦大学
