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Establishment of CYP2D6 Reference Samples by Multiple Validated Genotyping Platforms
Cytochrome P450 2D6 (cytochrome P450, family 2, subfamily D, polypeptide 6, or CYP2D6), a highly polymorphic drug metabolizing enzyme, is involved in the metabolism of one quarter of the most commonly prescribed medications. Here, we have applied multiple genotyping methods and Sanger sequencing to...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4237721/ https://www.ncbi.nlm.nih.gov/pubmed/24980783 http://dx.doi.org/10.1038/tpj.2014.27 |
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author | Fang, Hua Liu, Xiao Ramírez, Jacqueline Choudhury, Noura Kubo, Michiaki Im, Hae Kyung Konkashbaev, Anuar Cox, Nancy J. Ratain, Mark J. Nakamura, Yusuke O’Donnell, Peter H. |
author_facet | Fang, Hua Liu, Xiao Ramírez, Jacqueline Choudhury, Noura Kubo, Michiaki Im, Hae Kyung Konkashbaev, Anuar Cox, Nancy J. Ratain, Mark J. Nakamura, Yusuke O’Donnell, Peter H. |
author_sort | Fang, Hua |
collection | PubMed |
description | Cytochrome P450 2D6 (cytochrome P450, family 2, subfamily D, polypeptide 6, or CYP2D6), a highly polymorphic drug metabolizing enzyme, is involved in the metabolism of one quarter of the most commonly prescribed medications. Here, we have applied multiple genotyping methods and Sanger sequencing to assign precise and reproducible CYP2D6 genotypes, including copy numbers, for 48 HapMap samples. Furthermore, by analyzing a set of 50 human liver microsomes using endoxifen formation from N-desmethyl-tamoxifen as the phenotype of interest, we observed a significant positive correlation between CYP2D6 genotype-assigned activity score and endoxifen formation rate (r(s) = 0.68 by Rank correlation test, P = 5.3 ×10(−8)), which corroborated the genotype-phenotype prediction derived from our genotyping methodologies. In the future, these 48 publicly available HapMap samples characterized by multiple substantiated CYP2D6 genotyping platforms could serve as a reference resource for assay development, validation, quality control, and proficiency testing for other CYP2D6 genotyping projects, and for programs pursuing clinical pharmacogenomic testing implementation. |
format | Online Article Text |
id | pubmed-4237721 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
record_format | MEDLINE/PubMed |
spelling | pubmed-42377212015-06-01 Establishment of CYP2D6 Reference Samples by Multiple Validated Genotyping Platforms Fang, Hua Liu, Xiao Ramírez, Jacqueline Choudhury, Noura Kubo, Michiaki Im, Hae Kyung Konkashbaev, Anuar Cox, Nancy J. Ratain, Mark J. Nakamura, Yusuke O’Donnell, Peter H. Pharmacogenomics J Article Cytochrome P450 2D6 (cytochrome P450, family 2, subfamily D, polypeptide 6, or CYP2D6), a highly polymorphic drug metabolizing enzyme, is involved in the metabolism of one quarter of the most commonly prescribed medications. Here, we have applied multiple genotyping methods and Sanger sequencing to assign precise and reproducible CYP2D6 genotypes, including copy numbers, for 48 HapMap samples. Furthermore, by analyzing a set of 50 human liver microsomes using endoxifen formation from N-desmethyl-tamoxifen as the phenotype of interest, we observed a significant positive correlation between CYP2D6 genotype-assigned activity score and endoxifen formation rate (r(s) = 0.68 by Rank correlation test, P = 5.3 ×10(−8)), which corroborated the genotype-phenotype prediction derived from our genotyping methodologies. In the future, these 48 publicly available HapMap samples characterized by multiple substantiated CYP2D6 genotyping platforms could serve as a reference resource for assay development, validation, quality control, and proficiency testing for other CYP2D6 genotyping projects, and for programs pursuing clinical pharmacogenomic testing implementation. 2014-07-01 2014-12 /pmc/articles/PMC4237721/ /pubmed/24980783 http://dx.doi.org/10.1038/tpj.2014.27 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Fang, Hua Liu, Xiao Ramírez, Jacqueline Choudhury, Noura Kubo, Michiaki Im, Hae Kyung Konkashbaev, Anuar Cox, Nancy J. Ratain, Mark J. Nakamura, Yusuke O’Donnell, Peter H. Establishment of CYP2D6 Reference Samples by Multiple Validated Genotyping Platforms |
title | Establishment of CYP2D6 Reference Samples by Multiple Validated Genotyping Platforms |
title_full | Establishment of CYP2D6 Reference Samples by Multiple Validated Genotyping Platforms |
title_fullStr | Establishment of CYP2D6 Reference Samples by Multiple Validated Genotyping Platforms |
title_full_unstemmed | Establishment of CYP2D6 Reference Samples by Multiple Validated Genotyping Platforms |
title_short | Establishment of CYP2D6 Reference Samples by Multiple Validated Genotyping Platforms |
title_sort | establishment of cyp2d6 reference samples by multiple validated genotyping platforms |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4237721/ https://www.ncbi.nlm.nih.gov/pubmed/24980783 http://dx.doi.org/10.1038/tpj.2014.27 |
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