Target intelligence / Profile preview

FXYD domain-containing ion transport regulator 3 (FXYD3)

Target
FXYD3
Molecular classification
Ion transport regulator, Regulatory subunit of P-type ATPase, Membrane protein
01

Overview

FXYD domain-containing ion transport regulator 3 (FXYD3), also known as MAT-8 or mammary tumor 8 kDa protein, is a small membrane protein encoded by the *FXYD3* gene and a member of the FXYD protein family. FXYD3 associates with and modulates the activity and transport properties of the sodium/potassium-transporting ATPase (Na,K-ATPase), influencing sodium and potassium homeostasis in cells. It can also affect chloride conductance in certain experimental systems. FXYD3 is differentially expressed across tissues, including high levels in uterus, stomach, and colon, and is overexpressed in a range of human cancers, where it participates in regulating cell proliferation, apoptosis, and adhesion. The altered expression and regulatory effects on ion pumps have made FXYD3 a candidate biomarker for cancer diagnosis and prognosis, though it has not yet been validated as a direct drug target and few, if any, clinically actionable modulators are known.

Other names
MAT-8Mammary tumor 8 kDa proteinPhospholemman-like protein (PLML)Chloride conductance inducer protein Mat-8Sodium/potassium-transporting ATPase subunit FXYD3
02

Mechanism of action

Modulation of Na,K-ATPase activity and stability by direct association; Preventing pathologic glutathionylation of β1 subunit in Na,K-ATPase, particularly under oxidative stress; Induction or alteration of chloride conductance in some expression systems

03

Biological functions

Regulation of sodium/potassium-transporting ATPase (Na,K-ATPase)Regulation of ion transport and homeostasisModulation of chloride conductanceInfluences glycosylation processing of membrane ATPaseRegulation of cell proliferation, apoptosis, and cell adhesionProtection against oxidative stress (via glutathionylation effects)
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Disease associations

Cancer (notably breast, prostate, colorectal, pancreatic, esophageal squamous carcinoma, lung, glioma, and studied in hepatocellular carcinoma)May be relevant to other diseases involving ion imbalance or epithelial function
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Safety considerations

As a putative therapeutic target, modulation could disturb electrolyte homeostasis or epithelial barrier functionNo approved drugs; safety profile unknown, but targeting might risk disruption of ion transport in normal tissues
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Interacting drugs

None currently established as direct binders or clinically validated modulators; interventions in research use FXYD-derived peptides or siRNA
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Biomarkers

Overexpression is a biomarker in several cancers (breast, prostate, colorectal, pancreatic, hepatocellular, lung, glioma, and others)

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