Smoking and COX-2 Functional Polymorphisms Interact to Increase the Risk of Gastric Cardia Adenocarcinoma in Chinese Population
2011

Smoking and COX-2 Polymorphisms Increase Gastric Cancer Risk

Sample size: 1342 publication 10 minutes Evidence: moderate

Author Information

Author(s): Zhang Xue-Mei, Zhong Rong, Liu Li, Wang Ying, Yuan Ju-Xiang, Wang Peng, Sun Chuang, Zhang Zhi, Song Wen-Guang, Miao Xiao-Ping

Primary Institution: Ministry of Education Key Lab of Environment and Health, Tongji Medical College, Huazhong University of Science and Technology

Hypothesis

The study aimed to explore the interaction between smoking and functional polymorphisms of COX-2 in modulation of gastric cardia adenocarcinoma (GCA) risk.

Conclusion

The functional polymorphisms of COX-2, in interaction with smoking, may play a substantial role in the development of gastric cardia adenocarcinoma.

Supporting Evidence

  • Smokers had a 1.8 fold increased risk of GCA compared to non-smokers.
  • The –1195AA genotype was associated with a 1.50 increased risk of GCA.
  • The –765GC genotype conferred a 2.06 fold increased risk of GCA.
  • The 587Gly/Arg genotype was associated with a 1.67 fold increased risk of GCA.

Takeaway

This study found that certain genetic variations in a cancer-related gene, when combined with smoking, can increase the risk of a specific type of stomach cancer.

Methodology

A case-control study was conducted with genotyping of three COX-2 polymorphisms in 357 GCA patients and 985 controls, followed by multivariate logistic regression analysis.

Potential Biases

Potential selection bias in the recruitment of controls and cases.

Limitations

The study was limited to a specific population (Han Chinese) and may not be generalizable to other ethnic groups.

Participant Demographics

Participants were unrelated Han Chinese individuals, including 357 GCA patients and 985 cancer-free controls, matched by sex and age.

Statistical Information

P-Value

0.006

Confidence Interval

95% CI 1.05–2.13

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1371/journal.pone.0021894

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