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Therefore, we explored adenosine triphosphate\u2013binding cassette (ABC) and solute carriers family transporters expression (quantitative polymerase chain reaction) and protein abundance (liquid chromatography tandem mass spectrometry (<jats:styled-content style=\"fixed-case\">LC<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">MS<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">MS<\/jats:styled-content>)) in human liver and duodenum, jejunum, ileum, and colon in paired tissue specimens from nine organ donors. The transporter proteins were detected in the liver (permeability\u2010glycoprotein (P\u2010gp), multidrug resistance protein (<jats:styled-content style=\"fixed-case\">MRP<\/jats:styled-content>)2, <jats:styled-content style=\"fixed-case\">MRP<\/jats:styled-content>3, breast cancer resistance protein (<jats:styled-content style=\"fixed-case\">BCRP<\/jats:styled-content>), organic anion\u2010transporting polypeptide (<jats:styled-content style=\"fixed-case\">OATP<\/jats:styled-content>)1B1, <jats:styled-content style=\"fixed-case\">OATP<\/jats:styled-content>1B3, <jats:styled-content style=\"fixed-case\">OATP<\/jats:styled-content>2B1, organic cation transporter (<jats:styled-content style=\"fixed-case\">OCT<\/jats:styled-content>)1, <jats:styled-content style=\"fixed-case\">OCT<\/jats:styled-content>3, organic anion transporter 2, Na+\u2010taurocholate cotransporting polypeptide, monocarboxylate transporter (<jats:styled-content style=\"fixed-case\">MCT<\/jats:styled-content>)1, and multidrug and toxin extrusion 1) and the intestine (P\u2010gp, multidrug\u2010resistance protein (<jats:styled-content style=\"fixed-case\">MRP<\/jats:styled-content>)2, <jats:styled-content style=\"fixed-case\">MRP<\/jats:styled-content>3, <jats:styled-content style=\"fixed-case\">MRP<\/jats:styled-content>4, <jats:styled-content style=\"fixed-case\">BCRP<\/jats:styled-content>,<jats:styled-content style=\"fixed-case\"> OATP<\/jats:styled-content>2B1, <jats:styled-content style=\"fixed-case\">OCT<\/jats:styled-content>1, apical sodium\u2013bile acid transporter (only ileum), <jats:styled-content style=\"fixed-case\">MCT<\/jats:styled-content>1, and peptide transporter (<jats:styled-content style=\"fixed-case\">PEPT<\/jats:styled-content>1)). Significantly higher hepatic gene expression and protein abundance of <jats:italic><jats:styled-content style=\"fixed-case\">ABCC<\/jats:styled-content>2<\/jats:italic>\/<jats:styled-content style=\"fixed-case\">MRP<\/jats:styled-content>2, <jats:italic><jats:styled-content style=\"fixed-case\">SLC<\/jats:styled-content>22A1<\/jats:italic>\/<jats:styled-content style=\"fixed-case\">OCT<\/jats:styled-content>1, and <jats:italic><jats:styled-content style=\"fixed-case\">SLCO<\/jats:styled-content>2B1<\/jats:italic>\/<jats:styled-content style=\"fixed-case\">OATP<\/jats:styled-content>2B1 were found, as compared to all intestinal segments. No correlations between hepatic and small intestinal protein levels were observed. These observations provide a description of drug transporters distribution without the impact of interindividual variability bias and may help in construction of superior physiologically based pharmacokinetic and humanized animal models.<\/jats:p>","DOI":"10.1002\/cpt.1301","type":"journal-article","created":{"date-parts":[[2018,11,17]],"date-time":"2018-11-17T13:18:10Z","timestamp":1542460690000},"page":"1204-1212","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":123,"title":["Protein Abundance of Clinically Relevant Drug Transporters in the Human Liver and Intestine: A Comparative Analysis in Paired Tissue Specimens"],"prefix":"10.1111","volume":"105","author":[{"given":"Marek","family":"Drozdzik","sequence":"first","affiliation":[{"name":"Department of Experimental and Clinical Pharmacology Pomeranian Medical University  Szczecin 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