Table 1.
Gene Name | Genetic Aberration | Comments | References |
---|---|---|---|
NFKB1 | SNP_rs230521 | observed in GC patients | [32] |
SNP_rs28362491 (−94 ins/del ATTG) |
associated with diffuse GC, accelerate severe gastric inflammation | [33,34] | |
SNP_rs4648068 | increased risk of GC | [36,37] | |
homozygous deletion | invasive GC, gastric atrophy in mice | [38,39] | |
NFKB2 | homozygous deletion | gastric hyperplasia, early postnatal death | [40] |
suppressed in gastric mucosal lesions | [39] | ||
NFKBIA | SNP_rs2233408 T/C homozygote | GC susceptibility | [41] |
SNP_rs2233408 T heterozygote | reduced GC risk in intestinal-type non-cardiac GC | ||
SNP_rs17103265 | risk factor for gastric carcinogenesis | [42] | |
SNP_rs696 | cardia GC susceptibility | [43] | |
SNP_rs2233406 | non-cardia GC susceptibility | ||
I ΚBKB | SNP_rs2272736 A homozygote | prolonged overall survival time | [44] |
TNIP1 | SNP_rs7708392 | associated with GC risk | [45] |
SNP_rs10036748 | |||
MYD88 | deletion, mutation | gastric mucosal damage, carcinogenesis | [46] |
L265P mutant | observed in gastric mucosa-associated lymphoid tissue (MALT) lymphomas | [47] | |
RIPK2 | SNP_rs16900627 | increased risk of intestinal GC | [48] |
TLR9 | SNP_rs5743836 (−1237 T/C) |
associated with H. pylori-induced GC | [49] |