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Expression of thirty-six drug transporter genes in human intestine, liver, kidney, and organotypic cell lines

Hilgendorf, Constanze (author)
Ahlin, Gustav (author)
Uppsala universitet,Institutionen för farmaci
Seithel, Annick (author)
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Artursson, Per (author)
Uppsala universitet,Institutionen för farmaci
Ungell, Anna-Lena (author)
Karlsson, Johan (author)
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 (creator_code:org_t)
2007-05-11
2007
English.
In: Drug Metabolism And Disposition. - : American Society for Pharmacology & Experimental Therapeutics (ASPET). - 0090-9556 .- 1521-009X. ; 35:8, s. 1333-1340
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • This study was designed to quantitatively assess the mRNA expression of 36 important drug transporters in human jejunum, colon, liver, and kidney. Expression of these transporters in human organs was compared with expression in commonly used cell lines (Caco-2, HepG2, and Caki-1) originating from these organs to assess their value as in vitro transporter system models, and was also compared with data obtained from the literature on expression in rat tissues to assess species differences. Transporters that were highly expressed in the intestine included HPT1, PEPT1, BCRP, MRP2, and MDR1, whereas, in the liver, OCT1, MRP2, OATP-C, NTCP and BSEP were the main transporters. In the kidney, OAT1 was expressed at the highest levels, followed by OAT3, OAT4, MCT5, MDR1, MRP2, OCT2, and OCTN2. The best agreement between human tissue and the representative cell line was observed for human jejunum and Caco-2 cells. Expression in liver and kidney ortholog cell lines was not correlated with that in the associated tissue. Comparisons with rat transporter gene expression revealed significant species differences. Our results allowed a comprehensive quantitative comparison of drug transporter expression in human intestine, liver, and kidney. We suggest that it would be beneficial for predictive pharmacokinetic research to focus on the most highly expressed transporters. We hope that our comparison of rat and human tissue will help to explain the observed species differences in in vivo models, increase understanding of the impact of active transport processes on pharmacokinetics and distribution, and improve the quality of predictions from animal studies to humans.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmaceutiska vetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmaceutical Sciences (hsv//eng)

Keyword

Urinary system
Digestive system
Cell line
Established cell line
In vitro
Kidney
Liver
Gut
Human
Genetics
Gene
Carrier protein
Drug
PHARMACY
FARMACI

Publication and Content Type

ref (subject category)
art (subject category)

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