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Association between ITGA2 C807T polymorphism and gastric cancer risk.


ABSTRACT:

Aim

To evaluate the impact of the ITGA2 gene polymorphism on gastric cancer risk.

Methods

A hospital-based case-control study was conducted, including 307 gastric cancer patients and 307 age- and gender-matched control subjects. The genotypes were identified by polymerase chain reaction-restriction fragment length polymorphism assay.

Results

The frequencies of the wild and variant genotypes in cases were significantly different from those of controls (P = 0.019). Compared with individuals with the wild genotype CC, subjects with the variant genotypes (CT + TT) had a significantly higher risk of gastric cancer (adjusted odds ratio = 1.57, 95% CI = 1.13-2.17, P = 0.007). In stratified analyses, the elevated gastric cancer risk was especially evident in older individuals aged > 58 years, nonsmokers and rural subjects. Further analyses revealed that the variant genotypes were associated with poor tumor differentiation and adjacent organ invasion in the sub-analysis of gastric cancer patients.

Conclusion

The ITGA2 gene C807T polymorphism may be associated with an increased risk of gastric cancer, differentiation and invasion of gastric cancer.

SUBMITTER: Chen J 

PROVIDER: S-EPMC3120947 | biostudies-literature | 2011 Jun

REPOSITORIES: biostudies-literature

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Publications

Association between ITGA2 C807T polymorphism and gastric cancer risk.

Chen Jie J   Liu Nan-Nan NN   Li Jia-Qi JQ   Yang Li L   Zeng Ying Y   Zhao Xiao-Mei XM   Xu Lin-Lin LL   Luo Xuan X   Wang Bin B   Wang Xue-Rong XR  

World journal of gastroenterology 20110601 23


<h4>Aim</h4>To evaluate the impact of the ITGA2 gene polymorphism on gastric cancer risk.<h4>Methods</h4>A hospital-based case-control study was conducted, including 307 gastric cancer patients and 307 age- and gender-matched control subjects. The genotypes were identified by polymerase chain reaction-restriction fragment length polymorphism assay.<h4>Results</h4>The frequencies of the wild and variant genotypes in cases were significantly different from those of controls (P = 0.019). Compared w  ...[more]

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