Animal carcinogenicity and IARC Group 2B classification
In rat studies, potassium bromate caused renal tubular adenomas and carcinomas, thyroid follicular tumours, and peritoneal mesotheliomas in males. Mice showed a low incidence of kidney tumours in males, and hamsters showed a marginally increased incidence of renal tubular tumours. IARC reviewed this evidence in 1999 and classified potassium bromate as Group 2B, possibly carcinogenic to humans, based on sufficient evidence in animals but inadequate evidence in humans (no human epidemiological data were available).
Rats given potassium bromate in drinking water developed renal tubular adenomas and carcinomas, thyroid follicular tumours, and peritoneal mesotheliomas in males; the evidence in experimental animals was judged sufficient for carcinogenicity.
1999AnimalIARC Monographs on the Evaluation of Carcinogenic Risks to Humans, Volume 73
IARC classified potassium bromate as Group 2B, possibly carcinogenic to humans, noting inadequate evidence in humans but sufficient evidence in experimental animals.
1999Regulatory reviewIARC Monographs, Volume 73
Genotoxicity and oxidative DNA damage
Potassium bromate is genotoxic in multiple laboratory assays. It is clastogenic in hamster and rat cells in vitro, triggers micronucleus formation in rodents in vivo, and is genotoxic in experimental systems in vivo. Results in bacterial mutagenicity assays were equivocal. The primary mechanism appears to be oxidative: bromate generates reactive oxygen species in kidney tissue, producing oxidative DNA lesions including 8-hydroxydeoxyguanosine. This direct DNA damage mechanism is why regulators treat residues in food as unacceptable regardless of dose.
Potassium bromate was clastogenic in Chinese hamster and rat cells in vitro and induced micronucleus formation in mice in vivo; bacterial mutagenicity results were equivocal, with no firm conclusion drawn for mutagenicity in bacteria.
1999Lab + animalIARC Monographs, Volume 73
Potassium bromate produces lipid peroxidation and oxidative DNA damage in rat kidney, including induction of 8-hydroxydeoxyguanosine, indicating the carcinogenic mechanism involves oxidative DNA injury.
1999Lab + animalIARC Monographs, Volume 73
Residues in finished bread
The food industry argument for bromate was that it converts completely to bromide during baking and leaves no residue. Studies have shown this is not reliably the case. Measurable potassium bromate residues have been detected in commercially baked bread, particularly when oven temperatures are lower than ideal or loaves are denser. This unpredictability of residue elimination underpinned the UK and EU decisions to ban it.
Potassium bromate residues have been detected in finished baked bread products, demonstrating that complete conversion to bromide during baking cannot be guaranteed under real commercial conditions.
RegulatoryUK Ministry of Agriculture, Fisheries and Food (MAFF) review, cited in EU ban rationale