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Thiopurine methyltransferase (TPMT) genotyping to predict myelosuppression risk

Azathioprine (AZA), 6-mercaptopurine (6-MP), and thioguanine (TG) are thiopurine drugs. These agents are indicated for the treatment of various diseases including hematologic malignancies, inflammatory bowel disease (IBD), rheumatoid arthritis, and as immunosuppressants in solid organ transplants. T...

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Autores principales: Nguyen, Christine M., Mendes, Margaret A.S., Ma, Joseph D.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3094768/
https://www.ncbi.nlm.nih.gov/pubmed/21593964
http://dx.doi.org/10.1371/currents.RRN1236
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author Nguyen, Christine M.
Mendes, Margaret A.S.
Ma, Joseph D.
author_facet Nguyen, Christine M.
Mendes, Margaret A.S.
Ma, Joseph D.
author_sort Nguyen, Christine M.
collection PubMed
description Azathioprine (AZA), 6-mercaptopurine (6-MP), and thioguanine (TG) are thiopurine drugs. These agents are indicated for the treatment of various diseases including hematologic malignancies, inflammatory bowel disease (IBD), rheumatoid arthritis, and as immunosuppressants in solid organ transplants. Thiopurine drugs are metabolized, in part, by thiopurine methyltransferase (TPMT). TPMT displays genetic polymorphism resulting in null or decreased enzyme activity. At least 20 polymorphisms have been identified, of which, TPMT *2, *3A, *3B, *3C, and *4 are the most commonly studied. These polymorphisms have been associated with increased myelosuppression risk. TPMT genotyping may be useful to predict this risk.
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spelling pubmed-30947682011-05-17 Thiopurine methyltransferase (TPMT) genotyping to predict myelosuppression risk Nguyen, Christine M. Mendes, Margaret A.S. Ma, Joseph D. PLoS Curr Evidence on Genomic Tests Azathioprine (AZA), 6-mercaptopurine (6-MP), and thioguanine (TG) are thiopurine drugs. These agents are indicated for the treatment of various diseases including hematologic malignancies, inflammatory bowel disease (IBD), rheumatoid arthritis, and as immunosuppressants in solid organ transplants. Thiopurine drugs are metabolized, in part, by thiopurine methyltransferase (TPMT). TPMT displays genetic polymorphism resulting in null or decreased enzyme activity. At least 20 polymorphisms have been identified, of which, TPMT *2, *3A, *3B, *3C, and *4 are the most commonly studied. These polymorphisms have been associated with increased myelosuppression risk. TPMT genotyping may be useful to predict this risk. Public Library of Science 2011-05-15 /pmc/articles/PMC3094768/ /pubmed/21593964 http://dx.doi.org/10.1371/currents.RRN1236 Text en http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Evidence on Genomic Tests
Nguyen, Christine M.
Mendes, Margaret A.S.
Ma, Joseph D.
Thiopurine methyltransferase (TPMT) genotyping to predict myelosuppression risk
title Thiopurine methyltransferase (TPMT) genotyping to predict myelosuppression risk
title_full Thiopurine methyltransferase (TPMT) genotyping to predict myelosuppression risk
title_fullStr Thiopurine methyltransferase (TPMT) genotyping to predict myelosuppression risk
title_full_unstemmed Thiopurine methyltransferase (TPMT) genotyping to predict myelosuppression risk
title_short Thiopurine methyltransferase (TPMT) genotyping to predict myelosuppression risk
title_sort thiopurine methyltransferase (tpmt) genotyping to predict myelosuppression risk
topic Evidence on Genomic Tests
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3094768/
https://www.ncbi.nlm.nih.gov/pubmed/21593964
http://dx.doi.org/10.1371/currents.RRN1236
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