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Updated: Jun 23, 2026

High-Throughput Expression and Purification of Human Solute Carriers for Structural and Biochemical Studies
Published on: September 29, 2023
Solute carrier family 6 member 14 (SLC6A14): Expression, function, regulation, and impact on tumor progression
Wenchong Zang1, Zhentao Zhang2, Ye Zhi3
1Department of Pharmacology, College of Pharmaceutical Sciences, Zhejiang University of Technology, Hangzhou, China; Center for Clinical Pharmacy, Cancer Center, Department of Pharmacy, Zhejiang Provincial People's Hospital (Affiliated People's Hospital), Hangzhou Medical College, Hangzhou, China.
Insights
Solute carrier family 6 member 14 (SLC6A14) is upregulated in many cancers, driving tumor growth and immune evasion. Targeting SLC6A14 offers a dual therapeutic strategy for cancer intervention.
Area of Science:
- Molecular Biology
- Cancer Biology
- Biochemistry
Background:
- Solute carrier family 6 member 14 (SLC6A14) is a crucial amino acid transporter.
- It plays a vital role in cellular metabolism under both normal and disease states.
Purpose of the Study:
- To review the structural biology, regulation, and roles of SLC6A14 in cancer.
- To explore SLC6A14 as a therapeutic target for cancer intervention.
Main Methods:
- Systematic review of literature on SLC6A14.
- Analysis of SLC6A14 expression patterns in various cancers.
- Examination of SLC6A14's role in tumor progression and immune evasion.
Main Results:
- SLC6A14 is significantly upregulated in amino acid-dependent cancers like pancreatic, colorectal, and ER-positive breast cancer.
- It promotes tumor progression via multiple signaling pathways.
- SLC6A14 contributes to immune evasion through nutrient deprivation.
Conclusions:
- SLC6A14 is a key target for cancer therapy, impacting metabolism and immune regulation.
- A dual therapeutic strategy involving inhibition or prodrug delivery is proposed.
- Clinical translation requires mechanism-driven implementation rather than solely biomarker-driven stratification.
Abstract:
Solute carrier family 6 member 14 (SLC6A14/ATB0,+) is a broad-spectrum, Na+/Cl--dependent amino acid transporter. It mediates the active uptake of nearly all essential amino acids and serves as a critical metabolic hub under physiological and pathological conditions. To fully understand its potential as a therapeutic target for cancer intervention, this review systematically elucidates the structural biology, regulatory networks, and multifaceted roles of SLC6A14 in cancer. By examining the expression patterns of SLC6A14 in physiological and pathological situation, we demonstrate that it's significantly upregulated in various "amino acid-dependent" malignancies. It includes pancreatic cancer, colorectal cancer, and estrogen receptor-positive breast cancer, where it drives multiple signaling pathways and promotes tumor progression through diverse mechanisms. Beyond its classical metabolic functions, SLC6A14-mediated nutrient deprivation establishes a "nutrient-based immune evasion" mechanism, elucidating its potential for intervention in tumor immunity. Furthermore, we outline a dual-pronged therapeutic strategy for SLC6A14, including its use as a target for pharmacological inhibition and as a delivery channel for amino acid-conjugated prodrugs. Finally, we emphasize that successful clinical translation requires a shift from biomarker-driven patient stratification to mechanism-driven implementation. This highlights the central role of SLC6A14 as an intervenable target at the intersection of cancer metabolism, immune regulation, and targeted therapy.
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