Early detection of urinary bladder carcinogens in rats by immunohistochemistry for γ-H2AX: a review from analyses of 100 chemicals

• Published in: Journal of Toxicologic Pathology 2022, Vol.35(4), pp.283-298
• Main Authors: Toyoda, Takeshi, Ogawa, Kumiko
• Format: Article
• Language: English
• Subjects: Aldehyde dehydrogenase; Aldehydes; alternative method; Biomarkers; Bladder; Carcinogenesis; Carcinogenicity; Carcinogens; Damage detection; Deoxyribonucleic acid; DNA; DNA damage; early detection; Evaluation; Genotoxicity; Immunohistochemistry; Low level; Paraffin; Paraffins; Rats; Review; Safety; stem cell marker; Stem cells; Toxicity; Tumors; Urinary bladder; Urothelium; γ-H2AX
• ISSN: 0914-9198; 1881-915X; 1347-7404
• DOI: 10.1293/tox.2022-0061

In safety evaluations of chemicals, there is an urgent need to develop short-term methods to replace long-term carcinogenicity tests. We have reported that immunohistochemistry for γ-H2AX, a well-established biomarker of DNA damage, can detect bladder carcinogens at an early stage using histopathological specimens from 28-day repeated-dose oral toxicity studies in rats. Given the markedly low level of γ-H2AX formation in the bladder urothelium of untreated rats, an increase in γ-H2AX-positive cells following chemical exposure can be relatively easy to identify. Among the 100 compounds examined to date, bladder carcinogens can be detected with high sensitivity (33/39; 84.6%) and specificity (58/61; 95.1%). As expected, γ-H2AX formation levels tended to be high following exposure to genotoxic bladder carcinogens, whereas nongenotoxic bladder carcinogens also increased the number of γ-H2AX-positive cells, probably through secondary DNA damage associated with sustained proliferative stimulation. γ-H2AX formation in the bladder urothelium reflects species differences in susceptibility to bladder carcinogenesis between rats and mice and shows a clear dose-dependency associated with the intensity of tumor development as well as high reproducibility. Some of the bladder carcinogens that showed false-negative results in the evaluation of γ-H2AX alone could be detected by combined evaluation with immunostaining for bladder stem cell markers, including aldehyde dehydrogenase 1A1. This method may be useful for the early detection of bladder carcinogens, as it can be performed by simple addition of conventional immunostaining using formalin-fixed paraffin-embedded tissues from 28-day repeated-dose toxicity studies in rodents, which are commonly used in safety evaluations of chemical substances.