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Urinary Elimination of Coproporphyrins Is Dependent on ABCC2 Polymorphisms and Represents a Potential Biomarker of MRP2 Activity in Humans
MRP2 encoded by ABCC2 gene is involved in the secretion of numerous drugs and endogenous substrates. Patients with Dubin-Johnson syndrome due to mutation in ABCC2 gene have elevated urinary coproporphyrin ratio (UCP I/(I + III)). Here we investigated whether this ratio could serve as a biomarker of...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3085472/ https://www.ncbi.nlm.nih.gov/pubmed/21541183 http://dx.doi.org/10.1155/2011/498757 |
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author | Benz-de Bretagne, Isabelle Respaud, Renaud Vourc'h, Patrick Halimi, Jean-Michel Caille, Agnès Hulot, Jean-Sébastien Andres, Christian R. Le Guellec, Chantal |
author_facet | Benz-de Bretagne, Isabelle Respaud, Renaud Vourc'h, Patrick Halimi, Jean-Michel Caille, Agnès Hulot, Jean-Sébastien Andres, Christian R. Le Guellec, Chantal |
author_sort | Benz-de Bretagne, Isabelle |
collection | PubMed |
description | MRP2 encoded by ABCC2 gene is involved in the secretion of numerous drugs and endogenous substrates. Patients with Dubin-Johnson syndrome due to mutation in ABCC2 gene have elevated urinary coproporphyrin ratio (UCP I/(I + III)). Here we investigated whether this ratio could serve as a biomarker of MRP2 function. Phenotype-genotype relationships were studied in 74 healthy subjects by measuring individual UCP I/(I + III) ratio obtained on 24-hour urine and by analyzing five common SNPs in ABCC2 gene. The UCP I/(I + III) ratio varied from 14.7% to 46.0% in our population. Subjects with 3972TT genotype had a higher ratio (P = .04) than those carrying the C allele. This higher UCP I/(I + III) ratio was correlated with a higher level of isomer I excretion. This study provides a proof of concept that UCP I/(I + III) ratio can be used as a biomarker of MRP2 function in clinical studies as it provides quantitative information about the in vivo activity of MRP2 in a given patient. |
format | Text |
id | pubmed-3085472 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-30854722011-05-03 Urinary Elimination of Coproporphyrins Is Dependent on ABCC2 Polymorphisms and Represents a Potential Biomarker of MRP2 Activity in Humans Benz-de Bretagne, Isabelle Respaud, Renaud Vourc'h, Patrick Halimi, Jean-Michel Caille, Agnès Hulot, Jean-Sébastien Andres, Christian R. Le Guellec, Chantal J Biomed Biotechnol Research Article MRP2 encoded by ABCC2 gene is involved in the secretion of numerous drugs and endogenous substrates. Patients with Dubin-Johnson syndrome due to mutation in ABCC2 gene have elevated urinary coproporphyrin ratio (UCP I/(I + III)). Here we investigated whether this ratio could serve as a biomarker of MRP2 function. Phenotype-genotype relationships were studied in 74 healthy subjects by measuring individual UCP I/(I + III) ratio obtained on 24-hour urine and by analyzing five common SNPs in ABCC2 gene. The UCP I/(I + III) ratio varied from 14.7% to 46.0% in our population. Subjects with 3972TT genotype had a higher ratio (P = .04) than those carrying the C allele. This higher UCP I/(I + III) ratio was correlated with a higher level of isomer I excretion. This study provides a proof of concept that UCP I/(I + III) ratio can be used as a biomarker of MRP2 function in clinical studies as it provides quantitative information about the in vivo activity of MRP2 in a given patient. Hindawi Publishing Corporation 2011 2011-03-14 /pmc/articles/PMC3085472/ /pubmed/21541183 http://dx.doi.org/10.1155/2011/498757 Text en Copyright © 2011 Isabelle Benz-de Bretagne et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Benz-de Bretagne, Isabelle Respaud, Renaud Vourc'h, Patrick Halimi, Jean-Michel Caille, Agnès Hulot, Jean-Sébastien Andres, Christian R. Le Guellec, Chantal Urinary Elimination of Coproporphyrins Is Dependent on ABCC2 Polymorphisms and Represents a Potential Biomarker of MRP2 Activity in Humans |
title | Urinary Elimination of Coproporphyrins Is Dependent on ABCC2 Polymorphisms and Represents a Potential Biomarker of MRP2 Activity in Humans |
title_full | Urinary Elimination of Coproporphyrins Is Dependent on ABCC2 Polymorphisms and Represents a Potential Biomarker of MRP2 Activity in Humans |
title_fullStr | Urinary Elimination of Coproporphyrins Is Dependent on ABCC2 Polymorphisms and Represents a Potential Biomarker of MRP2 Activity in Humans |
title_full_unstemmed | Urinary Elimination of Coproporphyrins Is Dependent on ABCC2 Polymorphisms and Represents a Potential Biomarker of MRP2 Activity in Humans |
title_short | Urinary Elimination of Coproporphyrins Is Dependent on ABCC2 Polymorphisms and Represents a Potential Biomarker of MRP2 Activity in Humans |
title_sort | urinary elimination of coproporphyrins is dependent on abcc2 polymorphisms and represents a potential biomarker of mrp2 activity in humans |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3085472/ https://www.ncbi.nlm.nih.gov/pubmed/21541183 http://dx.doi.org/10.1155/2011/498757 |
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