Adverse outcome pathway (AOP): α2u-globulin nephropathy and kidney tumors in male rats

• Published in: Critical reviews in toxicology Vol. 52; no. 5; pp. 345 - 357
• Main Authors: Goyak, Katy O., Sarang, Satinder S., Franzen, A., Borghoff, Susan J., Ryman-Rasmussen, Jessica P.
• Format: Journal Article
• Language: English
• Published: England Taylor & Francis 28-05-2022
• Subjects: adverse outcome pathway; Adverse Outcome Pathways; Animals; Humans; key event; kidney; Kidney Neoplasms; Male; molecular initiating event; nephropathy; Rats; Risk Assessment; United States; α2u-Globulin; United States; kidney; nephropathy; adverse outcome pathway; key event; α2u-Globulin; molecular initiating event
• ISSN: 1040-8444; 1547-6898
• DOI: 10.1080/10408444.2022.2082269

The National Research Council's vision of using adverse outcome pathways (AOPs) as a framework to assist with toxicity assessment for regulatory requirements of chemical assessment has continued to gain traction since its release in 2007. The need to expand the AOP knowledge base has gained urgency, with the U.S. Environmental Protection Agency's directive to eliminate reliance on animal toxicity testing by 2035. To meet these needs, our goal was to elucidate the AOP for male-rat-specific kidney cancer. Male-rat-specific kidney tumors occur through the ability of structurally diverse substances to induce α2u-globulin nephropathy (α2u-N), a well-studied mode of action (MoA) not relevant in humans that results in kidney tumor formation in male rats. An accepted AOP may help facilitate the differentiation from other kidney tumors MoAs. Following identification and review of relevant in vitro and in vivo literature, both the MIE and subsequent KEs were identified. Based on the weight of evidence from the various resources, the confidence in this AOP is high. Uses of this AOP include hazard identification, development of in vitro assays to determine if the MoA is through α2u-N and not relevant to humans resulting in decreased use of animals, and regulatory applications.