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OCT3 promoter haplotype is associated with metformin pharmacokinetics in Koreans
Organic cation transporter 3 (OCT3) is expressed in various organs in humans and plays an important role in the transport of organic cations and drugs including metformin. In this study, we identified genetic variations of the OCT3 promoter and functionally characterized each variant by in vitro ass...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6240047/ https://www.ncbi.nlm.nih.gov/pubmed/30446679 http://dx.doi.org/10.1038/s41598-018-35322-6 |
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author | Kwon, Eun Young Chung, Jae-Yong Park, Hyo Jin Kim, Bo Min Kim, Minsuk Choi, Ji Ha |
author_facet | Kwon, Eun Young Chung, Jae-Yong Park, Hyo Jin Kim, Bo Min Kim, Minsuk Choi, Ji Ha |
author_sort | Kwon, Eun Young |
collection | PubMed |
description | Organic cation transporter 3 (OCT3) is expressed in various organs in humans and plays an important role in the transport of organic cations and drugs including metformin. In this study, we identified genetic variations of the OCT3 promoter and functionally characterized each variant by in vitro assays. Next, the association between the functional haplotype of the OCT3 promoter and pharmacokinetics of metformin was evaluated. In our study population, 7 variations and 2 major haplotypes were identified, of which H2 haplotype yielded a significantly higher luciferase activity than did the wild type. Two variants of H2, c.-1603G > A and c.-1547T > G, yielded significantly lower luciferase activities, whereas the luciferase activity of another variant, c.-29G > A, was significantly higher. Two transcription factors, Sp1 and USF1, were involved in the regulation of OCT3 transcription. Analysis of clinical data revealed that 25 subjects, either homozygous or heterozygous for H2, showed increased AUC(inf) and C(max) by 17.2% and 15.9%, respectively [P = 0.016 and 0.031, GMR (90% CI) = 1.17 (1.06–1.29) and 1.17 (1.04–1.31), respectively], compared to the 20 subjects in the control group. Our study suggests that an OCT3 promoter haplotype affects the pharmacokinetics of metformin in Koreans as well as the OCT3 transcription rate. |
format | Online Article Text |
id | pubmed-6240047 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62400472018-11-23 OCT3 promoter haplotype is associated with metformin pharmacokinetics in Koreans Kwon, Eun Young Chung, Jae-Yong Park, Hyo Jin Kim, Bo Min Kim, Minsuk Choi, Ji Ha Sci Rep Article Organic cation transporter 3 (OCT3) is expressed in various organs in humans and plays an important role in the transport of organic cations and drugs including metformin. In this study, we identified genetic variations of the OCT3 promoter and functionally characterized each variant by in vitro assays. Next, the association between the functional haplotype of the OCT3 promoter and pharmacokinetics of metformin was evaluated. In our study population, 7 variations and 2 major haplotypes were identified, of which H2 haplotype yielded a significantly higher luciferase activity than did the wild type. Two variants of H2, c.-1603G > A and c.-1547T > G, yielded significantly lower luciferase activities, whereas the luciferase activity of another variant, c.-29G > A, was significantly higher. Two transcription factors, Sp1 and USF1, were involved in the regulation of OCT3 transcription. Analysis of clinical data revealed that 25 subjects, either homozygous or heterozygous for H2, showed increased AUC(inf) and C(max) by 17.2% and 15.9%, respectively [P = 0.016 and 0.031, GMR (90% CI) = 1.17 (1.06–1.29) and 1.17 (1.04–1.31), respectively], compared to the 20 subjects in the control group. Our study suggests that an OCT3 promoter haplotype affects the pharmacokinetics of metformin in Koreans as well as the OCT3 transcription rate. Nature Publishing Group UK 2018-11-16 /pmc/articles/PMC6240047/ /pubmed/30446679 http://dx.doi.org/10.1038/s41598-018-35322-6 Text en © The Author(s) 2018 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Kwon, Eun Young Chung, Jae-Yong Park, Hyo Jin Kim, Bo Min Kim, Minsuk Choi, Ji Ha OCT3 promoter haplotype is associated with metformin pharmacokinetics in Koreans |
title | OCT3 promoter haplotype is associated with metformin pharmacokinetics in Koreans |
title_full | OCT3 promoter haplotype is associated with metformin pharmacokinetics in Koreans |
title_fullStr | OCT3 promoter haplotype is associated with metformin pharmacokinetics in Koreans |
title_full_unstemmed | OCT3 promoter haplotype is associated with metformin pharmacokinetics in Koreans |
title_short | OCT3 promoter haplotype is associated with metformin pharmacokinetics in Koreans |
title_sort | oct3 promoter haplotype is associated with metformin pharmacokinetics in koreans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6240047/ https://www.ncbi.nlm.nih.gov/pubmed/30446679 http://dx.doi.org/10.1038/s41598-018-35322-6 |
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