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Design and implementation of a novel pharmacogenetic assay for the identification of the CYP2D6*10 genetic variant
OBJECTIVES: Tamoxifen is considered to be the most widely used adjuvant therapy for hormone receptor positive breast cancer in premenopausal women. However, it is reported that nearly 30% of patients receiving tamoxifen therapy have shown reduced or no benefits. This may be due to the high inter-ind...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8925205/ https://www.ncbi.nlm.nih.gov/pubmed/35296326 http://dx.doi.org/10.1186/s13104-022-05993-6 |
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author | Ranadeva, Nadeeka Dimuthu Kumari Sirisena, Nirmala Dushyanthi Wetthasinghe, Tithila Kalum Noordeen, Nafeesa Dissanayake, Vajira Harshadeva Weerabaddana |
author_facet | Ranadeva, Nadeeka Dimuthu Kumari Sirisena, Nirmala Dushyanthi Wetthasinghe, Tithila Kalum Noordeen, Nafeesa Dissanayake, Vajira Harshadeva Weerabaddana |
author_sort | Ranadeva, Nadeeka Dimuthu Kumari |
collection | PubMed |
description | OBJECTIVES: Tamoxifen is considered to be the most widely used adjuvant therapy for hormone receptor positive breast cancer in premenopausal women. However, it is reported that nearly 30% of patients receiving tamoxifen therapy have shown reduced or no benefits. This may be due to the high inter-individual variations in the CYP2D6 gene that is involved in tamoxifen metabolism. The CYP2D6*10 gene variant (rs1065852C>T) is reported to be commonly found in Asian and South Asian populations. The present study was undertaken to design a novel pharmacogenetic assay (Single step-Tetra Arms Polymerase Chain Reaction) for the identification of the CYP2D6*10 variant and implement the designed assay by genotyping a cohort of breast cancer patients. RESULTS: The novel assay was successfully designed, optimized and validated using Sanger sequencing. Blood samples from 70 patients were genotyped. The following bands were observed in the gel image: Control band at 454 bp; band for C allele at 195 bp; band for T allele at 300 bp. The genotype frequencies for the CYP2D6*10 (rs1065852C>T) variant were: CC-24.28% (17/70), CT-75.71% (53/70), TT-0% (0/70). The allele frequencies were: T-allele-37.86% and C-allele-62.14%. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13104-022-05993-6. |
format | Online Article Text |
id | pubmed-8925205 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-89252052022-03-23 Design and implementation of a novel pharmacogenetic assay for the identification of the CYP2D6*10 genetic variant Ranadeva, Nadeeka Dimuthu Kumari Sirisena, Nirmala Dushyanthi Wetthasinghe, Tithila Kalum Noordeen, Nafeesa Dissanayake, Vajira Harshadeva Weerabaddana BMC Res Notes Research Note OBJECTIVES: Tamoxifen is considered to be the most widely used adjuvant therapy for hormone receptor positive breast cancer in premenopausal women. However, it is reported that nearly 30% of patients receiving tamoxifen therapy have shown reduced or no benefits. This may be due to the high inter-individual variations in the CYP2D6 gene that is involved in tamoxifen metabolism. The CYP2D6*10 gene variant (rs1065852C>T) is reported to be commonly found in Asian and South Asian populations. The present study was undertaken to design a novel pharmacogenetic assay (Single step-Tetra Arms Polymerase Chain Reaction) for the identification of the CYP2D6*10 variant and implement the designed assay by genotyping a cohort of breast cancer patients. RESULTS: The novel assay was successfully designed, optimized and validated using Sanger sequencing. Blood samples from 70 patients were genotyped. The following bands were observed in the gel image: Control band at 454 bp; band for C allele at 195 bp; band for T allele at 300 bp. The genotype frequencies for the CYP2D6*10 (rs1065852C>T) variant were: CC-24.28% (17/70), CT-75.71% (53/70), TT-0% (0/70). The allele frequencies were: T-allele-37.86% and C-allele-62.14%. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13104-022-05993-6. BioMed Central 2022-03-16 /pmc/articles/PMC8925205/ /pubmed/35296326 http://dx.doi.org/10.1186/s13104-022-05993-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Note Ranadeva, Nadeeka Dimuthu Kumari Sirisena, Nirmala Dushyanthi Wetthasinghe, Tithila Kalum Noordeen, Nafeesa Dissanayake, Vajira Harshadeva Weerabaddana Design and implementation of a novel pharmacogenetic assay for the identification of the CYP2D6*10 genetic variant |
title | Design and implementation of a novel pharmacogenetic assay for the identification of the CYP2D6*10 genetic variant |
title_full | Design and implementation of a novel pharmacogenetic assay for the identification of the CYP2D6*10 genetic variant |
title_fullStr | Design and implementation of a novel pharmacogenetic assay for the identification of the CYP2D6*10 genetic variant |
title_full_unstemmed | Design and implementation of a novel pharmacogenetic assay for the identification of the CYP2D6*10 genetic variant |
title_short | Design and implementation of a novel pharmacogenetic assay for the identification of the CYP2D6*10 genetic variant |
title_sort | design and implementation of a novel pharmacogenetic assay for the identification of the cyp2d6*10 genetic variant |
topic | Research Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8925205/ https://www.ncbi.nlm.nih.gov/pubmed/35296326 http://dx.doi.org/10.1186/s13104-022-05993-6 |
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