ABCG2 Single Nucleotide Polymorphism Affects Imatinib Pharmacokinetics in Lower Alpha-1-Acid Glycoprotein Levels in Humans
Imatinib is transported extracellularly by ABCB1 and ABCG2 efflux transporters and bound to alpha-1-acid glycoprotein (AGP) in the bloodstream. However, the clinical and pharmacokinetic effects of ABCB1 and ABCG2 on imatinib were inconsistent in the previous literature and have not been confirmed. T...
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Published in | Frontiers in pharmacology Vol. 12; p. 658039 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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29.04.2021
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ISSN | 1663-9812 1663-9812 |
DOI | 10.3389/fphar.2021.658039 |
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Abstract | Imatinib is transported extracellularly by ABCB1 and ABCG2 efflux transporters and bound to alpha-1-acid glycoprotein (AGP) in the bloodstream. However, the clinical and pharmacokinetic effects of ABCB1 and ABCG2 on imatinib were inconsistent in the previous literature and have not been confirmed. Therefore, in the present study, we explored the effects of the
ABCG2
and
ABCB1
genetic polymorphisms on imatinib pharmacokinetics in association with plasma AGP levels in healthy subjects. Twenty-seven healthy individuals were recruited, genotyped for
ABCG2
and
ABCB1
, and given a single oral dose of 400 mg imatinib. Plasma imatinib concentrations were measured and its pharmacokinetics was assessed with respect to
ABCG2
(c.421C>A and c.34G>A) and
ABCB1
(c.1236C>T, c.2677C>T/A, and c.3435C>T) genotypes, and plasma AGP levels. AGP levels showed a strong positive correlation with imatinib pharmacokinetics. ABCG2 c.421C>A single nucleotide polymorphism showed a statistically significant effect on imatinib pharmacokinetics in low plasma AGP levels groups (<80 mg/dl); subjects with high plasma AGP levels (n = 5, ≥80 mg/dl) were excluded. The results indicate that plasma AGP levels and
ABCG2
polymorphisms modulated imatinib pharmacokinetics; however, the effects of the ABCG2 transporter was masked at high plasma AGP levels. |
---|---|
AbstractList | Imatinib is transported extracellularly by ABCB1 and ABCG2 efflux transporters and bound to alpha-1-acid glycoprotein (AGP) in the bloodstream. However, the clinical and pharmacokinetic effects of ABCB1 and ABCG2 on imatinib were inconsistent in the previous literature and have not been confirmed. Therefore, in the present study, we explored the effects of the
ABCG2
and
ABCB1
genetic polymorphisms on imatinib pharmacokinetics in association with plasma AGP levels in healthy subjects. Twenty-seven healthy individuals were recruited, genotyped for
ABCG2
and
ABCB1
, and given a single oral dose of 400 mg imatinib. Plasma imatinib concentrations were measured and its pharmacokinetics was assessed with respect to
ABCG2
(c.421C>A and c.34G>A) and
ABCB1
(c.1236C>T, c.2677C>T/A, and c.3435C>T) genotypes, and plasma AGP levels. AGP levels showed a strong positive correlation with imatinib pharmacokinetics. ABCG2 c.421C>A single nucleotide polymorphism showed a statistically significant effect on imatinib pharmacokinetics in low plasma AGP levels groups (<80 mg/dl); subjects with high plasma AGP levels (n = 5, ≥80 mg/dl) were excluded. The results indicate that plasma AGP levels and
ABCG2
polymorphisms modulated imatinib pharmacokinetics; however, the effects of the ABCG2 transporter was masked at high plasma AGP levels. Imatinib is transported extracellularly by ABCB1 and ABCG2 efflux transporters and bound to alpha-1-acid glycoprotein (AGP) in the bloodstream. However, the clinical and pharmacokinetic effects of ABCB1 and ABCG2 on imatinib were inconsistent in the previous literature and have not been confirmed. Therefore, in the present study, we explored the effects of the ABCG2 and ABCB1 genetic polymorphisms on imatinib pharmacokinetics in association with plasma AGP levels in healthy subjects. Twenty-seven healthy individuals were recruited, genotyped for ABCG2 and ABCB1, and given a single oral dose of 400 mg imatinib. Plasma imatinib concentrations were measured and its pharmacokinetics was assessed with respect to ABCG2 (c.421C>A and c.34G>A) and ABCB1 (c.1236C>T, c.2677C>T/A, and c.3435C>T) genotypes, and plasma AGP levels. AGP levels showed a strong positive correlation with imatinib pharmacokinetics. ABCG2 c.421C>A single nucleotide polymorphism showed a statistically significant effect on imatinib pharmacokinetics in low plasma AGP levels groups (<80 mg/dl); subjects with high plasma AGP levels (n = 5, ≥80 mg/dl) were excluded. The results indicate that plasma AGP levels and ABCG2 polymorphisms modulated imatinib pharmacokinetics; however, the effects of the ABCG2 transporter was masked at high plasma AGP levels.Imatinib is transported extracellularly by ABCB1 and ABCG2 efflux transporters and bound to alpha-1-acid glycoprotein (AGP) in the bloodstream. However, the clinical and pharmacokinetic effects of ABCB1 and ABCG2 on imatinib were inconsistent in the previous literature and have not been confirmed. Therefore, in the present study, we explored the effects of the ABCG2 and ABCB1 genetic polymorphisms on imatinib pharmacokinetics in association with plasma AGP levels in healthy subjects. Twenty-seven healthy individuals were recruited, genotyped for ABCG2 and ABCB1, and given a single oral dose of 400 mg imatinib. Plasma imatinib concentrations were measured and its pharmacokinetics was assessed with respect to ABCG2 (c.421C>A and c.34G>A) and ABCB1 (c.1236C>T, c.2677C>T/A, and c.3435C>T) genotypes, and plasma AGP levels. AGP levels showed a strong positive correlation with imatinib pharmacokinetics. ABCG2 c.421C>A single nucleotide polymorphism showed a statistically significant effect on imatinib pharmacokinetics in low plasma AGP levels groups (<80 mg/dl); subjects with high plasma AGP levels (n = 5, ≥80 mg/dl) were excluded. The results indicate that plasma AGP levels and ABCG2 polymorphisms modulated imatinib pharmacokinetics; however, the effects of the ABCG2 transporter was masked at high plasma AGP levels. Imatinib is transported extracellularly by ABCB1 and ABCG2 efflux transporters and bound to alpha-1-acid glycoprotein (AGP) in the bloodstream. However, the clinical and pharmacokinetic effects of ABCB1 and ABCG2 on imatinib were inconsistent in the previous literature and have not been confirmed. Therefore, in the present study, we explored the effects of the and genetic polymorphisms on imatinib pharmacokinetics in association with plasma AGP levels in healthy subjects. Twenty-seven healthy individuals were recruited, genotyped for and , and given a single oral dose of 400 mg imatinib. Plasma imatinib concentrations were measured and its pharmacokinetics was assessed with respect to (c.421C>A and c.34G>A) and (c.1236C>T, c.2677C>T/A, and c.3435C>T) genotypes, and plasma AGP levels. AGP levels showed a strong positive correlation with imatinib pharmacokinetics. ABCG2 c.421C>A single nucleotide polymorphism showed a statistically significant effect on imatinib pharmacokinetics in low plasma AGP levels groups (<80 mg/dl); subjects with high plasma AGP levels (n = 5, ≥80 mg/dl) were excluded. The results indicate that plasma AGP levels and polymorphisms modulated imatinib pharmacokinetics; however, the effects of the ABCG2 transporter was masked at high plasma AGP levels. Imatinib is transported extracellularly by ABCB1 and ABCG2 efflux transporters and bound to alpha-1-acid glycoprotein (AGP) in the bloodstream. However, the clinical and pharmacokinetic effects of ABCB1 and ABCG2 on imatinib were inconsistent in the previous literature and have not been confirmed. Therefore, in the present study, we explored the effects of the ABCG2 and ABCB1 genetic polymorphisms on imatinib pharmacokinetics in association with plasma AGP levels in healthy subjects. Twenty-seven healthy individuals were recruited, genotyped for ABCG2 and ABCB1, and given a single oral dose of 400 mg imatinib. Plasma imatinib concentrations were measured and its pharmacokinetics was assessed with respect to ABCG2 (c.421C>A and c.34G>A) and ABCB1 (c.1236C>T, c.2677C>T/A, and c.3435C>T) genotypes, and plasma AGP levels. AGP levels showed a strong positive correlation with imatinib pharmacokinetics. ABCG2 c.421C>A single nucleotide polymorphism showed a statistically significant effect on imatinib pharmacokinetics in low plasma AGP levels groups (<80 mg/dl); subjects with high plasma AGP levels (n = 5, ≥80 mg/dl) were excluded. The results indicate that plasma AGP levels and ABCG2 polymorphisms modulated imatinib pharmacokinetics; however, the effects of the ABCG2 transporter was masked at high plasma AGP levels. |
Author | Park, Ji-Young Park, Jin-Woo Park, In-Hwan Kim, Jong-Min Lee, Sangjin Chung, Hyewon Kim, Kyoung-Ah |
AuthorAffiliation | 1 Department of Clinical Pharmacology and Toxicology, Anam Hospital, Korea University College of Medicine, Seoul , Korea 2 Department of Clinical Pharmacology and Toxicology, Guro Hospital, Korea University College of Medicine, Seoul , Korea |
AuthorAffiliation_xml | – name: 1 Department of Clinical Pharmacology and Toxicology, Anam Hospital, Korea University College of Medicine, Seoul , Korea – name: 2 Department of Clinical Pharmacology and Toxicology, Guro Hospital, Korea University College of Medicine, Seoul , Korea |
Author_xml | – sequence: 1 givenname: Jin-Woo surname: Park fullname: Park, Jin-Woo – sequence: 2 givenname: Hyewon surname: Chung fullname: Chung, Hyewon – sequence: 3 givenname: Kyoung-Ah surname: Kim fullname: Kim, Kyoung-Ah – sequence: 4 givenname: Jong-Min surname: Kim fullname: Kim, Jong-Min – sequence: 5 givenname: In-Hwan surname: Park fullname: Park, In-Hwan – sequence: 6 givenname: Sangjin surname: Lee fullname: Lee, Sangjin – sequence: 7 givenname: Ji-Young surname: Park fullname: Park, Ji-Young |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/33995081$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_3389_fphar_2024_1507915 crossref_primary_10_3389_fphar_2024_1400699 |
Cites_doi | 10.1182/blood-2007-10-116475 10.1002/jps.23614 10.1515/dmdi.2011.027 10.1158/1078-0432.ccr-10-2250 10.1038/sj.clpt.6100201 10.1007/s10637-008-9138-z 10.1016/j.bcmd.2011.11.001 10.2165/00003088-200544090-00001 10.1038/jhg.2010.98 10.1016/j.clinthera.2011.06.003 10.1056/nejmoa020461 10.1128/aac.01621-06 10.1182/blood-2004-04-1398 10.1016/j.ijbiomac.2020.02.151 10.1177/0091270003262101 10.1124/dmd.105.004283 10.1111/j.1476-5381.2010.00946.x 10.1182/blood-2006-07-036012 10.1159/000324900 10.1016/j.clpt.2006.05.003 10.2217/pgs.13.222 10.1111/j.1365-2125.2012.04422.x 10.1038/tpj.2014.54 10.2174/138945011795378487 10.1007/s00228-010-0916-0 10.1158/1078-0432.ccr-08-0950 10.1097/fpc.0b013e328360d10c 10.1158/0008-5472.can-04-2416 10.1200/jco.2008.20.4818 10.1111/j.1365-2710.2009.01127.x 10.1111/j.1365-2125.2006.02733.x 10.1111/j.1365-2125.2006.02719.x 10.1016/j.cca.2014.08.006 10.1093/annonc/mds532 10.4161/cc.3.12.1331 10.2174/138920013804870709 10.1038/nrd839 |
ContentType | Journal Article |
Copyright | Copyright © 2021 Park, Chung, Kim, Kim, Park, Lee and Park. Copyright © 2021 Park, Chung, Kim, Kim, Park, Lee and Park. 2021 Park, Chung, Kim, Kim, Park, Lee and Park |
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Keywords | STI-571 genetic polymorphism alpha-1 acid glycoprotein glivec imatinib (gleevec) ABCG2 (BCRP) |
Language | English |
License | Copyright © 2021 Park, Chung, Kim, Kim, Park, Lee and Park. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 This article was submitted to Drug Metabolism and Transport, a section of the journal Frontiers in Pharmacology Dora Koller, Yale University, United States These authors have contributed equally to this work and share first authorship Edited by: Sabina Passamonti, University of Trieste, Italy Reviewed by: Lukas Cerveny, Charles University, Czechia |
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SubjectTerms | ABCG2 (BCRP) alpha-1 acid glycoprotein genetic polymorphism glivec imatinib (gleevec) Pharmacology STI-571 |
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Title | ABCG2 Single Nucleotide Polymorphism Affects Imatinib Pharmacokinetics in Lower Alpha-1-Acid Glycoprotein Levels in Humans |
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