Target intelligence / Profile preview

Solute carrier family 41 member 1 (SLC41A1)

Target
SLC41A1
Molecular classification
Transporter, Solute carrier family, MgtE family of magnesium transporters, Ion channel (functionally, as some studies proposed it functions as a divalent cation channel)
01

Overview

Solute carrier family 41 member 1 (SLC41A1) is a eukaryotic magnesium transporter protein that belongs to the solute carrier (SLC) family 41 and is a vertebrate homolog of the prokaryotic MgtE magnesium transporters. It primarily functions as a Na⁺/Mg²⁺ exchanger on the plasma membrane, regulating magnesium efflux and cellular magnesium homeostasis. SLC41A1 is expressed most highly in the heart and testis, with lower expression in skeletal muscle and various tissues. It is involved in controlling intracellular magnesium concentrations, modulating cell survival, proliferation, and differentiation, and plays a role in mineralization processes in bone and in tumor suppression by promoting pro-apoptotic signaling. SLC41A1 dysregulation is associated with diseases such as pancreatic cancer, bone metabolic disorders, cardiovascular conditions, and metabolic syndrome. No approved drugs targeting SLC41A1 are identified as of this literature, but the protein is being investigated as a potential therapeutic or biomarker in relevant diseases.

Other names
MgtENPHPL2magnesium transporter protein SLC41A1solute carrier family 41 (magnesium transporter) member 1
02

Mechanism of action

SLC41A1 primarily functions as a Na⁺/Mg²⁺ exchanger, mediating magnesium efflux from cells. It modulates Akt/mTOR signaling in the context of cancer cell proliferation/apoptosis and influences Wnt signaling and β-catenin translocation in osteogenesis.

03

Biological functions

Magnesium ion (Mg²⁺) transport across plasma and potentially organellar membranesRegulation of cellular magnesium homeostasisRegulation of apoptosis (notably via mitochondrial membrane potential modulation and Bax/Bcl-2 signaling)Influence on osteogenic differentiation and mineralization in mesenchymal stem cells
04

Disease associations

Cancer (notably pancreatic ductal adenocarcinoma, where SLC41A1 acts as a tumor suppressor)Bone diseases/osteogenesis (MSC differentiation/mineralization)Metabolic syndromeDiabetes mellitusCardiovascular diseaseEssential hypertension
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Safety considerations

Dysregulation can lead to magnesium imbalance, affecting cardiovascular, metabolic, or skeletal systemsOverexpression or excessive activity may induce unwanted apoptosis or alter cell proliferation in non-target tissuesDownregulation may promote aberrant mineralization or affect bone health
06

Biomarkers

SLC41A1 expression level (potential biomarker for prognosis in pancreatic ductal adenocarcinoma, and possibly bone metabolic activity)

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