IUPHAR/BPS Guide to Pharmacology CITE
https://doi.org/10.2218/gtopdb/F238/2019.4
SLCO family of organic anion transporting polypeptides (version 2019.4) in the IUPHAR/BPS Guide to Pharmacology Database
Bruno Hagenbuch1
- University of Kansas, USA
Abstract
The SLCO superfamily is comprised of the organic anion transporting polypeptides (OATPs). The 11 human OATPs are divided into 6 families and ten subfamilies based on amino acid identity. These proteins are located on the plasma membrane of cells throughout the body. They have 12 TM domains and intracellular termini, with multiple putative glycosylation sites. OATPs mediate the sodium-independent uptake of a wide range of amphiphilic substrates, including many drugs and toxins. Due to the multispecificity of these proteins, this guide lists classes of substrates and inhibitors for each family member. More comprehensive lists of substrates, inhibitors, and their relative affinities may be found in the review articles listed below.
Contents
This is a citation summary for SLCO family of organic anion transporting polypeptides in the
Guide to Pharmacology
database (GtoPdb). It exists purely as an adjunct to the database to
facilitate the recognition of citations to and from the database by
citation analyzers. Readers will almost certainly want to visit the
relevant sections of the database which are given here under database
links.
GtoPdb is an expert-driven
guide to pharmacological targets and the substances that act on them.
GtoPdb is a reference work which is most usefully represented as an
on-line database. As in any publication this work should be
appropriately cited, and the papers it cites should also be
recognized. This document provides a citation for the relevant parts
of the database, and also provides a reference list for the research
cited by those parts.
Please note that the database version for the citations given in
GtoPdb are to the most recent preceding version
in which the family or its subfamilies and targets were substantially
changed. The links below are to the current version. If you
need to consult the cited version, rather than the most recent version, please contact
the GtoPdb curators.
Database links
SLCO family of organic anion transporting polypeptides
http://www.guidetopharmacology.org/GRAC/FamilyDisplayForward?familyId=238
Transporters
OATP1A2
http://www.guidetopharmacology.org/GRAC/ObjectDisplayForward?objectId=1219
OATP1B1
http://www.guidetopharmacology.org/GRAC/ObjectDisplayForward?objectId=1220
OATP1B3
http://www.guidetopharmacology.org/GRAC/ObjectDisplayForward?objectId=1221
OATP1C1
http://www.guidetopharmacology.org/GRAC/ObjectDisplayForward?objectId=1222
OATP2A1
http://www.guidetopharmacology.org/GRAC/ObjectDisplayForward?objectId=1223
OATP2B1
http://www.guidetopharmacology.org/GRAC/ObjectDisplayForward?objectId=1224
OATP3A1
http://www.guidetopharmacology.org/GRAC/ObjectDisplayForward?objectId=1225
OATP4A1
http://www.guidetopharmacology.org/GRAC/ObjectDisplayForward?objectId=1226
OATP4C1
http://www.guidetopharmacology.org/GRAC/ObjectDisplayForward?objectId=1227
OATP5A1
http://www.guidetopharmacology.org/GRAC/ObjectDisplayForward?objectId=1228
OATP6A1
http://www.guidetopharmacology.org/GRAC/ObjectDisplayForward?objectId=1229
References
- Bailey DG, Dresser GK, Leake BF and Kim RB. (2007) Naringin is a major and selective clinical inhibitor of organic anion-transporting polypeptide 1A2 (OATP1A2) in grapefruit juice. Clin. Pharmacol. Ther. 81: 495-502 [PMID:17301733]
- Chan BS, Satriano JA, Pucci M and Schuster VL. (1998) Mechanism of prostaglandin E2 transport across the plasma membrane of HeLa cells and Xenopus oocytes expressing the prostaglandin transporter "PGT". J. Biol. Chem. 273: 6689-97 [PMID:9506966]
- Fehrenbach T, Cui Y, Faulstich H and Keppler D. (2003) Characterization of the transport of the bicyclic peptide phalloidin by human hepatic transport proteins. Naunyn Schmiedebergs Arch. Pharmacol. 368: 415-20 [PMID:14530907]
- Fischer WJ, Altheimer S, Cattori V, Meier PJ, Dietrich DR and Hagenbuch B. (2005) Organic anion transporting polypeptides expressed in liver and brain mediate uptake of microcystin. Toxicol. Appl. Pharmacol. 203: 257-63 [PMID:15737679]
- Gui C, Obaidat A, Chaguturu R and Hagenbuch B. (2010) Development of a cell-based high-throughput assay to screen for inhibitors of organic anion transporting polypeptides 1B1 and 1B3. Curr Chem Genomics 4: 1-8 [PMID:20448812]
- Kanai N, Lu R, Satriano JA, Bao Y, Wolkoff AW and Schuster VL. (1995) Identification and characterization of a prostaglandin transporter. Science 268: 866-9 [PMID:7754369]
- Karlgren M, Vildhede A, Norinder U, Wisniewski JR, Kimoto E, Lai Y, Haglund U and Artursson P. (2012) Classification of inhibitors of hepatic organic anion transporting polypeptides (OATPs): influence of protein expression on drug-drug interactions. J. Med. Chem. 55: 4740-63 [PMID:22541068]
- Noé J, Portmann R, Brun ME and Funk C. (2007) Substrate-dependent drug-drug interactions between gemfibrozil, fluvastatin and other organic anion-transporting peptide (OATP) substrates on OATP1B1, OATP2B1, and OATP1B3. Drug Metab. Dispos. 35: 1308-14 [PMID:17470528]
- Treiber A, Schneiter R, Häusler S and Stieger B. (2007) Bosentan is a substrate of human OATP1B1 and OATP1B3: inhibition of hepatic uptake as the common mechanism of its interactions with cyclosporin A, rifampicin, and sildenafil. Drug Metab. Dispos. 35: 1400-7 [PMID:17496208]
- Vavricka SR, Van Montfoort J, Ha HR, Meier PJ and Fattinger K. (2002) Interactions of rifamycin SV and rifampicin with organic anion uptake systems of human liver. Hepatology 36: 164-72 [PMID:12085361]