Novel thiopurine S-methyltransferase (<i>TPMT</i>) variant identified in Malay individuals-Reference-Cited by-同舟云学术

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Novel thiopurine S-methyltransferase (TPMT) variant identified in Malay individuals

Published:2024-04-26 Issue: Volume: Page:
ISSN:1434-6621
Container-title:Clinical Chemistry and Laboratory Medicine (CCLM)
language:en
Short-container-title:

Author:

Lee Chun Kiat¹^ORCID,Huan Pei Tee²,Chai Chean Nee¹,Ng Li Jie¹,Koay Evelyn Siew-Chuan³,Lee Ogestelli Fabia⁴,Tan Malcolm⁵,Loh Tze Ping¹

Affiliation:

1. Department of Laboratory Medicine , 150744 National University Health System , Singapore , Singapore

2. Department of Paediatrics, Yong Loo Lin School of Medicine , 37580 National University of Singapore , Singapore , Singapore

3. Department of Pathology, Yong Loo Lin School of Medicine , 37580 National University of Singapore , Singapore , Singapore

4. School of Life and Physical Sciences , 464889 PSB Academy , Singapore , Singapore

5. Department of Gastroenterology and Hepatology , 37581 Singapore General Hospital , Singapore , Singapore

Publisher

Walter de Gruyter GmbH

Link

https://www.degruyter.com/document/doi/10.1515/cclm-2024-0494/pdf

Reference8 articles.

1. Lennard, L, Van Loon, JA, Weinshilboum, RM. Pharmacogenetics of acute azathioprine toxicity: relationship to thiopurine methyltransferase genetic polymorphism. Clin Pharmacol Ther 1989;46:149–54. https://doi.org/10.1038/clpt.1989.119.

2. Abaji, R, Krajinovic, M. Thiopurine S-methyltransferase polymorphisms in acute lymphoblastic leukemia, inflammatory bowel disease and autoimmune disorders: influence on treatment response. Pharmgenomics Pers Med 2017;10:143–56. https://doi.org/10.2147/pgpm.s108123.

3. Lee, CK, Loh, TP, Wong, ST, Lee, HK, Huan, PT, Chiu, LL, et al.. Detection of a novel single nucleotide polymorphism of the human thiopurine s-methyltransferase gene in a Chinese individual. Drug Metabol Pharmacokinet 2012;27:559–61. https://doi.org/10.2133/dmpk.dmpk-12-sc-008.

4. Lee, CK, Lee, HK, Huan, PT, Chiu, LL, Loh, TP, Koay, ESC. A point mutation in the thiopurine S-methyltransferase gene that led to exon 5 deletion in the transcribed mRNA. Clin Chem Lab Med 2016;54:e301–3. https://doi.org/10.1515/cclm-2015-1170.

5. Otterness, DM, Szumlanski, CL, Wood, TC, Weinshilboum, RM. Human thiopurine methyltransferase pharmacogenetics. Kindred with a terminal exon splice junction mutation that results in loss of activity. J Clin Invest 1998;101:1036–44. https://doi.org/10.1172/jci1004.

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