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NUDT15 polymorphisms alter thiopurine metabolism and hematopoietic toxicity

Open access
Moriyama, Takaya, Nishii, Rina, Perez-Andreu, Virginia, Yang, Wenjian, Klussmann, Federico Antillon, Zhao, Xujie, Lin, Ting-Nien, Hoshitsuki, Keito, Nersting, Jacob, Kihira, Kentaro, Hofmann, Ute, Komada, Yoshihiro, Kato, Motohiro, McCorkle, Robert, Li, Lie, Koh, Katsuyoshi, Najera, Cesar Rolando, Kham, Shirley Kow-Yin, Isobe, Tomoya, Chen, Zhiwei, Chiew, Edwynn Kean-Hui, Bhojwani, Deepa, Jeffries, Cynthia, Lu, Yan, Schwab, Matthias, Inaba, Hiroto, Pui, Ching-Hon, Relling, Mary V, Manabe, Atsushi, Hori, Hiroki, Schmiegelow, Kjeld, Yeoh, Allen E J, Evans, William E, Yang, Jun J·2016·Nature Genetics

Abstract

Widely used as anticancer and immunosuppressive agents, thiopurines have narrow therapeutic indices owing to frequent toxicities, partly explained by TPMT genetic polymorphisms. Recent studies identified germline NUDT15 variation as another critical determinant of thiopurine intolerance, but the underlying molecular mechanisms and the clinical implications of this pharmacogenetic association remain unknown. In 270 children enrolled in clinical trials for acute lymphoblastic leukemia in Guatemala, Singapore and Japan, we identified four NUDT15 coding variants (p.Arg139Cys, p.Arg139His, p.Val18Ile and p.Val18_Val19insGlyVal) that resulted in 74.4–100% loss of nucleotide diphosphatase activity. Loss-of-function NUDT15 diplotypes were consistently associated with thiopurine intolerance across the three cohorts (P = 0.021, 2.1 × 10−5 and 0.0054, respectively; meta-analysis P = 4.45 × 10−8, allelic effect size = −11.5). Mechanistically, NUDT15 inactivated thiopurine metabolites and decreased thiopurine cytotoxicity in vitro, and patients with defective NUDT15 alleles showed excessive levels of thiopurine active metabolites and toxicity. Taken together, these results indicate that a comprehensive pharmacogenetic model integrating NUDT15 variants may inform personalized thiopurine therapy.

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Metadata

Authors
Moriyama, T., Nishii, R., Perez-Andreu, V., Yang, W., Klussmann, F. A., Zhao, X., Lin, T.-N., Hoshitsuki, K., Nersting, J., Kihira, K., Hofmann, U., Komada, Y., Kato, M., McCorkle, R., Li, L., Koh, K., Najera, C. R., Kham, S. K.-Y., Isobe, T., Chen, Z., Chiew, E. K.-H., Bhojwani, D., Jeffries, C., Lu, Y., Schwab, M., Inaba, H., Pui, C.-H., Relling, M. V., Manabe, A., Hori, H., Schmiegelow, K., Yeoh, A. E. J., Evans, W. E., & Yang, J. J.
Venue
Nature Genetics
Published
2016-02-15
Volume
48
Issue
4
Pages
367-373
ISSN
  • 1061-4036 (ISSN-L)
  • 1546-1718
OpenAlex
W2275947820
Cited by
477
References
54
FWCI
58.87
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: NUDT15 polymorphisms alter thiopurine metabolism and hematopoietic toxicity. https://app.cochat.ai/papers/10.1038/ng.3508
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Moriyama, T., Nishii, R., Perez-Andreu, V., Yang, W., Klussmann, F. A., Zhao, X., Lin, T.-N., Hoshitsuki, K., Nersting, J., Kihira, K., Hofmann, U., Komada, Y., Kato, M., McCorkle, R., Li, L., Koh, K., Najera, C. R., Kham, S. K.-Y., Isobe, T., . . . Yang, J. J. (2016). NUDT15 polymorphisms alter thiopurine metabolism and hematopoietic toxicity. Nature Genetics. https://doi.org/10.1038/ng.3508

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