AI Article Synopsis

  • * Some research reveals conflicting views on how activating a pathway (HIF) may influence tumor development, with some suggesting it helps tumors grow and others suggesting it may reduce tumor growth.
  • * In studies on transgenic mice and rats receiving various doses of vadadustat over extended periods, the tumors found were deemed statistically unrelated to the treatment, suggesting that vadadustat does not have a carcinogenic effect in these animals.

Article Abstract

Vadadustat is an investigational oral hypoxia-inducible factor (HIF) prolyl-4-hydroxylase inhibitor to treat anemia due to chronic kidney disease (CKD). Some studies suggest that HIF activation promotes tumorigenesis by activating angiogenesis downstream of vascular endothelial growth factor, while other studies suggest that elevated HIF activity may produce an antitumor phenotype. To evaluate the potential carcinogenicity of vadadustat in mice and rats, we dosed CByB6F1/Tg.rasH2 hemizygous (transgenic) mice orally by gavage with 5 to 50 mg/kg/d of vadadustat for 6 months and dosed Sprague-Dawley rats orally by gavage with 2 to 20 mg/kg/d for approximately 85 weeks. Doses were selected based on the maximally tolerated dose established for each species in previous studies. The tumors that were identified in the studies were not considered to be treatment-related for statistical reasons or within the historical control range. There was no carcinogenic effect attributed to vadadustat in mice or rats.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10278385PMC
http://dx.doi.org/10.1177/01926233231168836DOI Listing

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