Table 2.
Main mechanism of gastric cancer induced by each kind of heavy metal.
| Heavy metals | Main mechanism | Reference |
|---|---|---|
| Cd | (1) Disrupt the stomach mucosal barrier | [19–21, 23, 24, 26–30] |
| (2) DNA damage via ROS | ||
| (3) Ineffective DNA repair | ||
| (4) Alter catalase activity | ||
| (5) Accelerate cancer development | ||
|
| ||
| As | (1) Cell damage | [23, 24, 30–33] |
| (2) Inhibit DNA repair | ||
| (3) Epigenome | ||
| (4) Enhanced cancer development by inducing overexpressing of miRNAs | ||
|
| ||
| Hg | (1) DNA damage | [24, 28, 34–36] |
| (2) Chromosomal aberration | ||
| (3) Induce immune dysfunction | ||
|
| ||
| Pb | (1) DNA damage via ROS | [22–24, 28, 30, 37–39] |
| (2) Ineffective DNA repair and inhibiting DNA repair with UItraviolet rays | ||
| (3) Promote tumorigenesis via Il-8 | ||
| (4) Change catalase activity | ||
| (5) Enhanced cancer development by inducing overexpressing of miRNAs | ||
|
| ||
| Cr | (1) DNA lesion | [23, 24, 32, 33, 40–42] |
| (2) Gene abnormalities | ||
| (3) Promote cancer cell migration and invasion | ||