| First Author | Wang JP | Year | 2002 |
| Journal | Toxicol Lett | Volume | 133 |
| Issue | 1 | Pages | 17-31 |
| PubMed ID | 12076507 | Mgi Jnum | J:77147 |
| Mgi Id | MGI:2181105 | Doi | 10.1016/s0378-4274(02)00086-3 |
| Citation | Wang JP, et al. (2002) A review of animal models for the study of arsenic carcinogenesis. Toxicol Lett 133(1):17-31 |
| abstractText | As inorganic arsenic is a proven human carcinogen, significant effort has been made in recent decades in an attempt to understand arsenic carcinogenesis using animal models, including rodents (rats and mice) and larger mammals such as beagles and monkeys. Transgenic animals were also used to test the carcinogenic effect of arsenicals, but until recently all models had failed to mimic satisfactorily the actual mechanism of arsenic carcinogenicity. However, within the past decade successful animal models have been developed using the most common strains of mice or rats. Thus dimethylarsinic acid (DMA), an organic arsenic compound which is the major metabolite of inorganic arsenicals in mammals, has been proven to be tumorigenic in such animals. Reports of successful cancer induction in animals by inorganic arsenic (arsenite and arsenate) have been rare, and most carcinogenetic studies have used organic arsenicals such as DMA combined with other tumor initiators. Although such experiments used high concentrations of arsenicals for the promotion of tumors, animal models using doses of arsenicals species closed to the exposure level of humans in endemic areas are obviously the most significant. Almost all researchers have used drinking water or food as the pathway for the development of animal model test systems in order to mimic chronic arsenic poisoning in humans; such pathways seem more likely to achieve desirable results. |
