Target intelligence / Profile preview

Solute carrier organic anion transporter family member 4A1 (SLCO4A1)

Target
SLCO4A1
Molecular classification
Transporter, Solute carrier family (specifically SLC, organic anion transporting polypeptide subgroup)
01

Overview

Solute carrier organic anion transporter family member 4A1 (SLCO4A1, also known as OATP4A1) is a 12-transmembrane domain protein and a member of the organic anion-transporting polypeptide (OATP) family within the solute carrier (SLC) superfamily[1][2]. Predominantly localized to the plasma membrane, it is expressed in a variety of normal tissues (highest in heart and placenta, and notable in liver, kidney, lung, and others), as well as in tumors such as colorectal and ovarian cancers[2][3][4]. SLCO4A1 mediates sodium-independent cellular uptake of a broad spectrum of amphiphilic organic anions, including endogenous hormones (such as thyroid hormones, estrogens), prostaglandins (notably PGE2), bile acids, and various drugs and xenobiotic compounds[1][2][3]. Increased SLCO4A1 expression is linked to pro-inflammatory signaling and cancer cell proliferation, invasion, and poor clinical prognosis in colorectal cancer[3][4]. Its activity may influence drug response and efficacy through the uptake of specific chemotherapeutic agents, and variability in its expression or genetic polymorphisms could affect disease progression and patient outcomes[4][5].

Other names
OATP4A1OATP-EOATPEOATP-RP1OATPRP1POATSLC21A12Colon organic anion transporterOrganic anion transporter polypeptide-related protein 1Organic anion-transporting polypeptide ESodium-independent organic anion transporter E
02

Mechanism of action

Facilitates sodium-independent uptake of a wide range of endogenous and exogenous organic anions into target cells, including hormones, metabolites, and drugs Modulates local availability of signaling molecules (e.g., prostaglandins, steroid hormones) by uptake and subsequent intracellular degradation or reutilization, potentially altering inflammatory and cancer-related signaling

03

Biological functions

Organic anion transmembrane transportProstaglandin transmembrane transportUptake of steroid hormone conjugates (e.g., estrone sulfate, estradiol glucuronide)Thyroid hormone transport (e.g., T3, T4, rT3)Bile acid transport (e.g., taurocholate)Uptake of xenobiotics and various drugsRegulation of cellular signaling by controlling extracellular prostaglandin and hormone levels
04

Disease associations

Cancer (notably colorectal cancer and ovarian cancer)Inflammation (e.g., inflammatory bowel disease)Potential roles in other diseases such as Kawasaki disease and primary hypertrophic osteoarthropathy
05

Safety considerations

Potential drug-drug interactions due to multispecific substrate uptake (notably if drugs compete for transport)Variability in expression may affect drug absorption, efficacy, toxicity, and systemic exposure in cancer and other conditionsPolymorphisms may alter transporter function and influence disease risk or drug response
06

Interacting drugs

Anticancer drugs (multiple poorly specified; SLCO4A1 is known to transport several drugs, but individual drugs need further confirmation in specific reports)

4 more in the full profile.

07

Biomarkers

Prognostic marker in colorectal cancer: higher expression is associated with poorer survival and more aggressive diseaseMarker of activated inflammatory pathways in high-grade serous ovarian cancer

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