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Meta-Analysis
. 2017 Mar 28;23(12):2234-2245.
doi: 10.3748/wjg.v23.i12.2234.

Association between COX-2 -1195G>A polymorphism and gastrointestinal cancer risk: A meta-analysis

Affiliations
Meta-Analysis

Association between COX-2 -1195G>A polymorphism and gastrointestinal cancer risk: A meta-analysis

Xiao-Wei Zhang et al. World J Gastroenterol. .

Abstract

Aim: To perform a meta-analysis to investigate the association between cyclooxygenase-2 (COX-2) -1195G>A gene polymorphism and gastrointestinal cancers.

Methods: Publications related to the COX-2 -1195G>A gene polymorphism and gastrointestinal cancers published before July 2016 were retrieved from PubMed, EMBASE, Web of Science, China Biological Medicine Database, China National Knowledge Infrastructure, and CQVIP Database. Meta-analysis was performed using Stata11.0 software. The strength of the association was evaluated by calculating the combined odds ratios (ORs) and the corresponding 95%CIs. The retrieved publications were excluded or included one by one for sensitivity analysis. In addition, the funnel plot, Begg's rank correlation test, and Egger's linear regression method were applied to analyse whether the included publications had publication bias.

Results: A total of 24 publications related to the COX-2 -1195G>A gene polymorphism were included, including 28 studies involving 11043 cases and 18008 controls. The meta-analysis results showed that the COX-2 -1195G>A gene polymorphism significantly correlated with an increased risk of gastrointestinal cancers, particularly gastric cancer (A vs G: OR = 1.35; AA/AG vs GG: OR = 1.54; AA vs GG/AG: OR = 1.43; AA vs GG: OR = 1.80; AG vs GG: OR = 1.35). Compared to the Caucasian population in America and Europe, the COX-2 -1195G>A gene polymorphism in the Asian population (A vs G: OR = 1.30; AA/AG vs GG: OR = 1.50; AA vs GG/AG: OR = 1.35; AA vs GG: OR = 1.71; AG vs GG: OR = 1.37) significantly increased gastrointestinal cancer risk. The sensitivity analysis (P < 0.05) and the false positive report probability (P < 0.2) confirmed the reliability of the results.

Conclusion: The results showed that the COX-2 -1195G>A gene polymorphism might be a potential risk factor for gastrointestinal cancers. Further validation by a large homogeneous study is warranted.

Keywords: -1195G>A; COX-2; Gastrointestinal cancer; Meta-analysis; Polymorphism.

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Conflict of interest statement

Conflict-of-interest statement: The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
Flow chart of literature inclusion and exclusion.
Figure 2
Figure 2
Forest plot of the stratified analysis of the COX-2 -1195G>A dominant model (AA/AG vs GG) and susceptibility to gastrointestinal cancers in different tumour types.
Figure 3
Figure 3
Forest plot of stratified analysis of the COX-2 -1195G>A dominant model (AA/AG vs GG) and gastrointestinal cancer susceptibility in different populations.
Figure 4
Figure 4
Analysis of the influence of a single study on the total combined OR in the dominant model (AA/AG vs GG).
Figure 5
Figure 5
Cumulative meta-analysis of the COX-2 -1195G>A polymorphism and gastrointestinal cancer susceptibility in the dominant model (AA/AG vs GG).
Figure 6
Figure 6
Begg’s funnel plot of the publication bias in the COX-2 -1195G>A dominant model (AA/AG vs GG).

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