| Literature DB >> 31155393 |
Miaki Uzu1, Miki Nonaka1, Kanako Miyano1, Hiromi Sato2, Nagomi Kurebayashi3, Kazuyoshi Yanagihara4, Takashi Sakurai3, Akihiro Hisaka2, Yasuhito Uezono5.
Abstract
Cancer cachexia is a systemic wasting syndrome characterized by anorexia and loss of body weight. The xanthine oxidase (XO) inhibitor febuxostat is one of the promising candidates for cancer cachexia treatment. However, cachexic symptoms were not alleviated by oral administration of febuxostat in our cancer cachexia model. Metabolomic analysis with brains of our cachexic model showed that purine metabolism was activated and XO activity was increased, and thus suggested that febuxostat would not reach the brain. Accordingly, targeting XO in the brain, which controls appetite, may be an effective strategy for treatment of cancer cachexia.Entities:
Keywords: Cancer cachexia; Metabolome; Xanthine oxidase
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Year: 2019 PMID: 31155393 DOI: 10.1016/j.jphs.2019.04.005
Source DB: PubMed Journal: J Pharmacol Sci ISSN: 1347-8613 Impact factor: 3.337