Table 1.
First author | Year of publication | Quality assessment scores | Genotyping method | Total sample size | Number of controls | Number of cases | Study location | Ethnic group | P values for HWE | Controls, genotypes(n) | All Cases, genotypes(n) | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CC | CT | TT | CC | CT | TT | ||||||||||
Wu MS | 2003 | 7 | Direct sequencing | 450 | 230 | 220 | China | Asians | 0.231397685 | 20 | 83 | 127 | 27 | 105 | 88 |
Savage SA# | 2004 | 5 | ABI Genetic Analyzer | 466 | 382 | 84 | China | Asians | 0.314869012 | 49 | 163 | 170 | 9 | 38 | 37 |
Alpízar-Alpízar W | 2005 | 6 | Pyrosequencing | 90 | 45 | 45 | Costa Rica | Latinos | 0.08326454 | 18 | 24 | 3 | 25 | 16 | 4 |
Zambon CF^ | 2005 | 5 | TaqMan | 773 | 644 | 129 | Italy | Caucasians | 0.696436614 | 353 | 245 | 46 | 70 | 42 | 17 |
Kamangar F#^¶ | 2006 | 8 | TaqMan | 250 | 152 | 98 | Finland | Caucasians | 0.66272429 | 80 | 62 | 10 | 58 | 35 | 5 |
Sugimoto M#^*¶+ | 2007 | 6.5 | ASP | 273 | 168 | 105 | Japan | Asians | 0.194224595 | 9 | 73 | 86 | 6 | 57 | 42 |
Crusius JB#^ | 2008 | 8.5 | ABI real-time PCR | 1323 | 1094 | 229 | European | Caucasians | 0.02386503 | 636 | 378 | 80 | 145 | 72 | 12 |
Xiao H | 2009 | 6 | RFLP | 844 | 624 | 220 | China | Asians | 0.718880427 | 69 | 283 | 272 | 20 | 100 | 100 |
Ko KP | 2009 | 7 | SNaPshot | 409 | 326 | 83 | Korea | Asians | 0.038333741 | 37 | 121 | 168 | 11 | 33 | 39 |
Su SP | 2010 | 6.5 | RFLP | 143 | 100 | 43 | China | Asians | 0.433216715 | 6 | 43 | 51 | 4 | 21 | 18 |
Liu J+ | 2011 | 6.5 | RFLP | 477 | 243 | 234 | China | Asians | 0.772829993 | 28 | 106 | 109 | 39 | 96 | 99 |
#Data of cardia-subtype gastric cancer were accessible; ^ Data of noncardia-subtype gastric cancer were accessible; * Data of sporadic diffuse-subtype gastric cancer were accessible; ¶ Data of intestinal-subtype gastric cancer were accessible. +Data of the status of Helicobacter pylori of gastric cancer were accessible. RFLP: Restriction fragment length polymorphisms; TaqMan: 5'nuclease polymerase chain reaction assays; Pyrosequencing: a method of DNA sequencing (determining the order of nucleotides in DNA) based on the "sequencing by synthesis" principle. It differs from Sanger sequencing, in that it relies on the detection of pyrophosphate release on nucleotide incorporation, rather than chain termination with dideoxynucleotides; Direct sequencing: method of methylation analysis using bisulfite-treated DNA utilized PCR and standard dideoxynucleotide DNA sequencing to directly determine the nucleotides resistant to bisulfite conversion; ASP: the allele specific primer-polymerase chain reaction (ASP-PCR) method; SNaPshot: the SNaPshot assay which provides detection of certain SNPs