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 inFrontiers in pharmacology Vol. 12; p. 658039
Main Authors Park, Jin-Woo, Chung, Hyewon, Kim, Kyoung-Ah, Kim, Jong-Min, Park, In-Hwan, Lee, Sangjin, Park, Ji-Young
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 29.04.2021
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ISSN1663-9812
1663-9812
DOI10.3389/fphar.2021.658039

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Summary: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.
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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
ISSN:1663-9812
1663-9812
DOI:10.3389/fphar.2021.658039