Journal
ACTA PHARMACOLOGICA SINICA
Volume 43, Issue 7, Pages 1623-1632Publisher
NATURE PUBL GROUP
DOI: 10.1038/s41401-021-00800-7
Keywords
xanthine oxidoreductase (XOR); ROS; uric acid; cancer therapy
Funding
- National Natural Science Foundation of China [81773760, 81973345]
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XOR plays a critical role in gout, hyperuricemia, and cancer by controlling purine metabolism and influencing oxidative stress and inflammatory responses. Its dual roles in promoting and inhibiting tumor growth make it a significant target for cancer therapy.
Xanthine oxidoreductase (XOR) is a critical, rate-limiting enzyme that controls the last two steps of purine catabolism by converting hypoxanthine to xanthine and xanthine to uric acid. It also produces reactive oxygen species (ROS) during the catalytic process. The enzyme is generally recognized as a drug target for the therapy of gout and hyperuricemia. The catalytic products uric acid and ROS act as antioxidants or oxidants, respectively, and are involved in pro/anti-inflammatory actions, which are associated with various disease manifestations, including metabolic syndrome, ischemia reperfusion injury, cardiovascular disorders, and cancer. Recently, extensive efforts have been devoted to understanding the paradoxical roles of XOR in tumor promotion. Here, we summarize the expression of XOR in different types of cancer and decipher the dual roles of XOR in cancer by its enzymatic or nonenzymatic activity to provide an updated understanding of the mechanistic function of XOR in cancer. We also discuss the potential to modulate XOR in cancer therapy.
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