Target intelligence / Profile preview

Solute carrier family 22 member 7 (SLC22A7)

Target
SLC22A7
Molecular classification
Transporter, Membrane protein, Major facilitator superfamily (MFS) transporter
01

Overview

Solute carrier family 22 member 7 (SLC22A7), commonly called organic anion transporter 2 (OAT2), is a sodium-independent transmembrane transporter protein highly expressed in the liver and kidney, and to a lesser extent in lung and other tissues[2][3][4][8]. It mediates the bidirectional transport of a wide variety of organic anions and cations, including endogenous substances (e.g., urate, glutamate, creatinine, nucleotides, prostaglandins) and many drugs (e.g., methotrexate, antibiotics, antivirals)[2][3][8]. SLC22A7 is an integral membrane protein, localized to the basolateral membrane of hepatocytes and renal proximal tubule cells, where it plays a key role in drug disposition, elimination of toxins, and regulation of cGMP signaling[1][3][6][7]. SLC22A7 is associated with genetic disorders of metabolism (gout, bilirubin metabolic disorders) and is increasingly recognized for its importance in clinical pharmacology, serving as a biomarker for drug response and a potential target for modulating chemotherapy efficacy and safety[8].

Other names
Organic anion transporter 2OAT2hOAT2Novel liver transporterNLTOrganic anion transporter 11hOAT11Liver-specific transporter
02

Mechanism of action

Inhibition or modulation of organic anion exchange activity; Alteration of renal or hepatic excretion of drugs and metabolites; Regulation of intracellular and extracellular cGMP levels (which may impact cGMP-dependent signaling)[6][7]

03

Biological functions

Transmembrane transport of organic anions and cationsSodium-independent organic anion transportcGMP transmembrane transport and regulationGlutamate/orotate exchangeRenal and hepatic secretion of endogenous and exogenous compoundsXenobiotic metabolic process
04

Disease associations

GoutBilirubin metabolic disorderDrug disposition and pharmacokinetics (implicated in responses to chemotherapy in colorectal cancer[8])
05

Safety considerations

Drug-drug interactions due to competition or inhibition of transporter activityAccumulation of toxic endogenous or therapeutic compounds if transporter function is compromisedAltered drug disposition contributing to variability in efficacy or toxicity
06

Interacting drugs

Methotrexate

8 more in the full profile.

07

Biomarkers

SLC22A7 expression serves as a biomarker for predicting response to combination chemotherapy in colorectal cancer[8]Expression/profile may act as a marker for hepatic or renal transporter function

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