Nudt15-mediated inflammatory signaling contributes to divergent outcomes in leukemogenesis and hematopoiesis
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Publisher
Springer Science and Business Media LLC
Link
https://www.nature.com/articles/s41375-024-02352-1.pdf
Reference35 articles.
1. Takagi Y, Setoyama D, Ito R, Kamiya H, Yamagata Y, Sekiguchi M. Human MTH3 (NUDT18) protein hydrolyzes oxidized forms of guanosine and deoxyguanosine diphosphates: comparison with MTH1 and MTH2. J Biol Chem. 2012;287:21541–9.
2. Hori M, Satou K, Harashima H, Kamiya H. Suppression of mutagenesis by 8-hydroxy-2’-deoxyguanosine 5’-triphosphate (7,8-dihydro-8-oxo-2’-deoxyguanosine 5’-triphosphate) by human MTH1, MTH2, and NUDT5. Free Radic Biol Med. 2010;48:1197–201.
3. Moriyama T, Nishii R, Perez-Andreu V, Yang W, Klussmann FA, Zhao X, et al. NUDT15 polymorphisms alter thiopurine metabolism and hematopoietic toxicity. Nat Genet. 2016;48:367–73.
4. Kakuta Y, Kawai Y, Okamoto D, Takagawa T, Ikeya K, Sakuraba H, et al. NUDT15 codon 139 is the best pharmacogenetic marker for predicting thiopurine-induced severe adverse events in Japanese patients with inflammatory bowel disease: a multicenter study. J Gastroenterol. 2018;53:1065–78.
5. Nishii R, Moriyama T, Janke LJ, Yang W, Suiter CC, Lin TN, et al. Preclinical evaluation of NUDT15-guided thiopurine therapy and its effects on toxicity and antileukemic efficacy. Blood. 2018;131:2466–74.
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