Table 2.
Genomic variants identified to be associated with esophageal squamous cell carcinoma
| Loci associated with ESCC | Method/design | Case sample size | Control sample size | Ref. |
| PLCE1 (10q23 rs227422) and C20orf54 (20p13) | GWAS | 1077 | 1733 | Wang et al[22] |
| ALDH2 (4q21-23, rs671) and ADH1B (12q24, rs1229984) | GWAS | 1070 | 2836 | Cui et al[23] |
| PLCE1 (10q23 rs2274223) | GWAS | 2115 | 3302 | Abnet et al[24] |
| ALDH2 (4q23, rs671) and ADH1B (12q24.11–13, rs1229984) | GWAS | 1071 | 2762 | Tanaka et al[25] |
| 5q11 (rs10052657) 21q22 (rs2014300), 6p21 (rs10484761), 10q23 (rs2274223), and 12q24 (rs2074356, rs11066280) CYP1A1 A2455G polymorphism(Ile/Val, rs1048943) | GWAS | 2031 1881 | 2044 3786 | Wu et al[26] Shen et al[27] |
| Meta-analysis | ||||
| (13 case-control studies) | ||||
| CYP1A1/CYP2E1 (MTHFR) C677T and A1298C polymorphisms with ESCC | Case-control study | 565 /482 3213 | 468/466 4354 | Wang et al[28] Fang et al[29] |
| Meta-analysis | ||||
| (15 case-control studies) | ||||
| rs1014867 polymorphisms in FAT4 gene | Case-control study | 2139 | 2273 | Du et al[30] |
| Interleukin 1B rs16944 | Case-control study | 380 | 380 | Zheng et al[31] |
| CHRNA5-A3-B4 rs667282 TT/TG | Case-control study | 866 | 952 | Wang et al[32] |
| rs1494961, rs1229984 and rs1789924, and rs671 | Case-control study | 2139 | 2273 | Gao et al[33] |
| Genetic variants in DNA repair pathway genes/(EGFR) signaling pathway | Case-control study | 1942 | 2111 | Li et al[34], Li et al[35] |
| Sex hormone metabolic genes | Case-control study | 1026 | 1452 | Hyland et al[36] |
| Chromosome 1 open reading frame 10 (C1orf10) | Case-control study | 991 | 984 | Zhang et al[37] |
ESCC: Esophageal squamous cell carcinoma; GWAS: Genome wide association studies; PLCE1: Phospholipase C epsilon 1; C20orf54: Chromosome 20 open reading frame 54; ADH1B: Alcohol dehydrogenase; ALDH2: Acetaldehyde dehydrogenase.