| Literature DB >> 32996603 |
Willy Albert Flegel1, Kshitij Srivastava1, Tristan Michael Sissung2, Barry Ronald Goldspiel3, William Douglas Figg2.
Abstract
The PharmacoScan pharmacogenomics platform screens for variation in genes that affect drug absorption, distribution, metabolism, elimination, immune adverse reactions and targets. Among the 1,191 genes tested on the platform, 12 genes are expressed in the red cell membrane: ABCC1, ABCC4, ABCC5, ABCG2, CFTR, SLC16A1, SLC19A1, SLC29A1, ATP7A, CYP4F3, EPHX1 and FLOT1. These genes represent 5 ATP-binding cassette proteins, 3 solute carrier proteins, 1 ATP transport protein and 3 genes associated with drug metabolism and adverse drug reactions. Only ABCG2 and SLC29A1 encode blood group systems, JR and AUG, respectively. We propose red cells as an ex vivo model system to study the effect of heritable variants in genes encoding the transport proteins on the pharmacokinetics of drugs. Altered pharmacodynamics in red cells could also cause adverse reactions, such as haemolysis, hitherto unexplained by other mechanisms. © Published 2020. This article is a U.S. Government work and is in the public domain in the USA.Entities:
Keywords: DMET; PharmacoScan; drug transporters; erythrocytes; pharmacogenetics; pharmacogenomics
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Year: 2020 PMID: 32996603 PMCID: PMC9108996 DOI: 10.1111/vox.12999
Source DB: PubMed Journal: Vox Sang ISSN: 0042-9007 Impact factor: 2.996