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Meta‐analysis: tumour invasion‐related genetic polymorphisms and gastric cancer susceptibility
Author(s) -
GAO L.,
NIETERS A.,
BRENNER H.
Publication year - 2008
Publication title -
alimentary pharmacology and therapeutics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.308
H-Index - 177
eISSN - 1365-2036
pISSN - 0269-2813
DOI - 10.1111/j.1365-2036.2008.03760.x
Subject(s) - meta analysis , medicine , cdh1 , genetic association , genotype , cancer , genetic predisposition , oncology , genome wide association study , genetics , gene , biology , single nucleotide polymorphism , disease , cell , cadherin
Summary Background Host genetic susceptibility has been suggested as one of the most important possible explanations for interindividual difference in gastric cancer (GC) risk. Aim To evaluate the impact of tumour invasion‐related gene polymorphisms, which may be involved in a variety of processes during GC development, such as cell adhesion and angiogenesis, on the risk of GC. Methods We reviewed published studies on tumour invasion‐related gene polymorphisms and GC susceptibility until 31 March 2008, and then quantitatively summarized associations of the most widely‐studied polymorphism, CDH1 −160C>A, with GC using meta‐analysis. Results Twenty‐seven eligible studies were included in this review. Fourteen polymorphisms significantly related to GC in at least one study were identified. For several polymorphisms, heterogeneous results were observed and associations in opposite directions were seen among Asian and Caucasian populations. In meta‐analysis, CDH1 −160C>A showed an inverse association with GC among Asians (OR, 0.76; 95% CI, 0.55–1.05) and a positive association among Caucasians (OR, 1.40; 95% CI, 0.95–2.04). Conclusions This review suggests that genetic polymorphisms in tumour invasion could be candidate biomarkers of GC risk. However, differences between populations and stages of cancer need to be taken into account and may explain some of the inconsistencies found in previous studies.