Please use this identifier to cite or link to this item: http://scholarbank.nus.edu.sg/handle/10635/106624
Title: Clinical pharmacogenomics of thiopurine S-methyltransferase.
Authors: Zhou, S. 
Issue Date: Jan-2006
Citation: Zhou, S. (2006-01). Clinical pharmacogenomics of thiopurine S-methyltransferase.. Current clinical pharmacology 1 (1) : 119-128. ScholarBank@NUS Repository.
Abstract: Thiopurine methyltransferase (TPMT) catalyzes the S-methylation of thiopurine drugs such as 6-mercaptopurine (6-MP), thioguanine and azathioprine (AZA). These drugs are used to treat conditions such as acute lymphoblastic leukemia, inflammatory bowel disease, rheumatoid arthritis, and organ transplant rejection. This review highlights the polymorphisms of TPMT gene and their clinical impact on the use of thiopurine drugs. To date, there are 18 known mutational TPMT alleles. The three main TPMT alleles, namely TPMT *2, *3A and *3C, account for 80 - 95% of the intermediate and low enzyme activity. The TPMT gene exhibits significant genetic polymorphisms among all ethnic groups studied. Patients who inherited very low levels of TPMT activity are at greatly increased risk for thiopurine-induced toxicity such as myelosuppression, when treated with standard doses of these drugs, while subjects with very high activity may be undertreated. Moreover, clinical drug interactions may occur due to TMPT induction or inhibition. Identification of the TPMT mutant alleles allows physicians to tailor the dosage of the thiopurine drugs to the genotype of the patient or to use alternatives, improving therapeutic outcome.
Source Title: Current clinical pharmacology
URI: http://scholarbank.nus.edu.sg/handle/10635/106624
ISSN: 15748847
Appears in Collections:Staff Publications

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