Target intelligence / Profile preview

Sodium-dependent organic anion transporter (SLC10A6)

Target
SLC10A6
Molecular classification
Transporter, Solute carrier (SLC) family member, Sodium-coupled symporter
01

Overview

Sodium-dependent organic anion transporter (SLC10A6, also known as SOAT) is a transmembrane sodium-coupled transporter specialized in importing monosulfated steroid hormones (such as estrone sulfate and dehydroepiandrosterone sulfate) from the extracellular space into target cells, enabling local steroid hormone activation via the sulfatase pathway. SLC10A6 is a member of the solute carrier 10 (SLC10) family but, unlike the classic bile acid transporters (NTCP/SLC10A1, ASBT/SLC10A2), its physiological substrates are primarily sulfated steroids, with negligible transport of common bile acids. It has nine transmembrane domains and is highly expressed in hormone-responsive tissues as well as adipose tissues, and its expression is regulated in response to inflammation, adipogenesis, and potentially by nuclear receptors. Mutant mice lacking SLC10A6 display altered adipocyte physiology, implicating it in metabolic regulation. SLC10A6 is being studied for its potential role in steroid-responsive cancers (e.g., breast cancer), adipose tissue function, and overall endocrine regulation, but is not currently a therapeutic drug target.

Other names
SOATSolute carrier family 10 member 6Sodium-dependent organic anion transporterSolute carrier family 10 (sodium/bile acid cotransporter) member 6
02

Mechanism of action

Sodium-coupled co-transport of 3′- and 17′-monosulfated steroid hormones into cells, providing precursor molecules for local (intracrine) synthesis of active estrogens and androgens.

03

Biological functions

Transport of sulfated steroid hormones (e.g., estrone sulfate, dehydroepiandrosterone sulfate)Regulation of intracrine steroid metabolismSodium-dependent uptake of organic anionsModulation of adipocyte lipid accumulationInvolvement in hormone-responsive tissue function
04

Disease associations

Cancer (notably hormone-dependent breast cancer)Obesity and adipocyte hypertrophyInflammation-associated metabolic changes
05

Safety considerations

Potential off-target effects on systemic steroid hormone balance if inhibitedInsufficient data for therapeutic safety profile as a direct targetUnknown impact of long-term modulation on adipose tissue function and cancer biology
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Interacting drugs

No approved drugs are known to target SLC10A6 directly as of the latest literature; experimental inhibitors and substrate analogs have been described (e.g., sulfated steroids used to study transport)
07

Biomarkers

SLC10A6 expression levels may serve as a biomarker for hormone-responsive breast cancer and inflammation-related changes in adipose tissue, but this is investigational and not clinically established

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