Target intelligence / Profile preview

Amino acid transporter system ASC (ASC transporter)

Target
ASC transporter
Molecular classification
Transporter, Solute carrier (SLC) family, Amino acid transporter
01

Overview

Amino acid transporter system ASC refers primarily to a family of sodium-dependent neutral amino acid transporters that preferentially mediate the exchange of small neutral amino acids—including alanine, serine, cysteine, and threonine—across the plasma membrane[2][5]. The system consists of two main subtypes: **ASCT1 (SLC1A4)** and **ASCT2 (SLC1A5)**, which share partial substrate overlap and belong to the solute carrier (SLC) superfamily[1][2]. ASCT1 is ubiquitously expressed with a notable role in CNS neurotransmitter regulation and brain development[2], while ASCT2 is highly expressed in rapidly proliferating cells and is upregulated in many cancers, fulfilling increased glutamine demands[1]. System ASC transporters are considered important therapeutic targets, especially in oncology and neurobiology, due to their central roles in nutrient uptake, neurotransmission, and cellular metabolism[1][3][2]. Experimental inhibitors of ASCT2 are being studied as anticancer agents and modulators of neuronal function; however, broad biological activity raises challenges for selective targeting and safety[1][3].

Other names
Alanine-serine-cysteine transporterASCTAlanine-serine-cysteine transporter 1 (ASCT1; SLC1A4)Alanine-serine-cysteine transporter 2 (ASCT2; SLC1A5)Asc-type amino acid transporter 1SLC7A10 (Asc-1; mostly CNS)Neutral amino acid transporter A
02

Mechanism of action

Competitive inhibition of substrate binding; Blocking glutamine or neutral amino acid transport; Modulation of neurotransmitter levels

03

Biological functions

Amino acid transportRegulation of neurotransmitter homeostasisGlutamine uptakeGlutamatergic and glycinergic neurotransmissionCell proliferation and nutrient supply
04

Disease associations

CancerNeurodevelopmental disorders (e.g., microcephaly, schizophrenia, ALS)Neurodegenerative diseaseInflammationVisual disturbancesAmyotrophic lateral sclerosis
05

Safety considerations

Potential CNS toxicity due to disruption of serine/glycine balanceRisk of impairing tumor cell metabolism versus normal cell functionMetabolic side effects due to widespread expression in proliferative tissues
06

Interacting drugs

Few specific drugs under development—experimental ASC inhibitors (e.g., V-9302, benzylserine derivatives, L-γ-glutamyl-p-nitroanilide)

1 more in the full profile.

07

Biomarkers

ASCT2 (SLC1A5) expression in tumors as marker of glutamine dependencySLC1A4/ASCT1 levels in neurodevelopmental disordersASC transporter activity in neuroscience or oncology research

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