Target intelligence / Profile preview

Solute carrier family 26 member 6 (SLC26A6)

Target
SLC26A6
Molecular classification
Transporter, Anion exchanger, Solute carrier family 26
01

Overview

Solute carrier family 26 member 6 (SLC26A6), also known as Putative anion transporter 1 (PAT1), is a multifunctional anion exchanger primarily expressed on the apical membranes of epithelial cells in the kidney, intestine, and pancreas [1, 6, 15]. It plays a critical role in maintaining ion homeostasis and acid-base balance by mediating the exchange of various anions, most notably chloride, bicarbonate, and oxalate [1, 5, 10]. In the intestine, SLC26A6 is a major pathway for oxalate secretion, and its dysfunction or deficiency is strongly linked to hyperoxaluria and the formation of calcium oxalate kidney stones [1, 5, 9]. Beyond its role in mineral metabolism, it is involved in fluid absorption in the gut and bicarbonate secretion in the pancreas, often working in coordination with the cystic fibrosis transmembrane conductance regulator (CFTR) [1, 5, 12]. Recent research has also identified SLC26A6 as a potential oncogene in hepatocellular carcinoma and a target for treating intestinal hyposecretory disorders like those seen in cystic fibrosis [4, 12]. Pharmacological modulation of SLC26A6, particularly through novel selective inhibitors like PAT1inh-B01, offers therapeutic potential for managing conditions ranging from constipation to metabolic stone diseases, though safety concerns regarding systemic oxalate balance must be carefully managed [5, 12].

Other names
Putative anion transporter 1PAT1Chloride/formate exchangerCFEXPendrin-like protein 1Pendrin-L1Sulfate anion transporterAnion exchange transporter
02

Mechanism of action

Inhibition of anion exchange and blockade of intestinal fluid absorption.

03

Biological functions

Anion exchangeIon homeostasisAcid-base balanceFluid absorptionOxalate secretionIntracellular pH regulation
04

Disease associations

NephrolithiasisHyperoxaluriaHepatocellular carcinomaCystic fibrosisArrhythmiaFetal skeletal dysplasia
05

Safety considerations

HyperoxalemiaKidney stone formationArrhythmiaAcid-base imbalance
06

Interacting drugs

PAT1inh-B01

3 more in the full profile.

07

Biomarkers

Urinary oxalatePlasma oxalate

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