Your browser doesn't support javascript.
loading
Pharmacogenomics with red cells: a model to study protein variants of drug transporter genes.
Flegel, Willy Albert; Srivastava, Kshitij; Sissung, Tristan Michael; Goldspiel, Barry Ronald; Figg, William Douglas.
Afiliação
  • Flegel WA; Department of Transfusion Medicine, NIH Clinical Center, National Institutes of Health, Bethesda, MD, USA.
  • Srivastava K; Department of Transfusion Medicine, NIH Clinical Center, National Institutes of Health, Bethesda, MD, USA.
  • Sissung TM; Clinical Pharmacology Program, Office of the Clinical Director, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
  • Goldspiel BR; Clinical Trials Operations and Informatics Branch, Cancer Therapy Evaluation Program, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
  • Figg WD; Clinical Pharmacology Program, Office of the Clinical Director, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Vox Sang ; 116(2): 141-154, 2021 Feb.
Article em En | MEDLINE | ID: mdl-32996603
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.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas de Membrana Transportadoras / Farmacogenética / Polimorfismo Genético / Antígenos de Grupos Sanguíneos / Transportadores de Cassetes de Ligação de ATP / Eritrócitos Limite: Humans Idioma: En Revista: Vox Sang Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas de Membrana Transportadoras / Farmacogenética / Polimorfismo Genético / Antígenos de Grupos Sanguíneos / Transportadores de Cassetes de Ligação de ATP / Eritrócitos Limite: Humans Idioma: En Revista: Vox Sang Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos