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SLC1A5 is a Key Regulator of Glutamine Metabolism and a Prognostic Marker for Aggressive Luminal Breast Cancer

Alfarsi, Lutfi H.; El Ansari, Rokaya; Erkan, Busra; Fakroun, Ali; Craze, Madeleine L.; Aleskandarany, Mohammed A.; Cheng, Kiu Wai; Ellis, Ian O.; Rakha, Emad A.; Green, Andrew R.

SLC1A5 is a Key Regulator of Glutamine Metabolism and a Prognostic Marker for Aggressive Luminal Breast Cancer Thumbnail


Authors

Lutfi H. Alfarsi

Rokaya El Ansari

Busra Erkan

Ali Fakroun

Madeleine L. Craze

Mohammed A. Aleskandarany

Kiu Wai Cheng

Ian O. Ellis



Abstract

Cancer cells exhibit altered metabolism, often relying on glutamine (Gln) for growth. Breast cancer (BC) is a heterogeneous disease with varying clinical outcomes. We investigated the role of the amino acid transporter SLC1A5 (ASCT2) and its association with BC subtypes and patient outcomes. In large BC cohorts, SLC1A5 mRNA (n = 9488) and SLC1A5 protein (n = 1274) levels were assessed and correlated their expression with clinicopathological features, molecular subtypes, and patient outcomes. In vitro SLC1A5 knockdown and inhibition studies in luminal BC cell lines (ZR-75-1 and HCC1500) were used to further explore the role of SLC1A5 in Gln metabolism. Statistical analysis was performed using chi-squared tests, ANOVA, Spearman’s correlation, Kaplan–Meier analysis, and Cox regression. SLC1A5 mRNA and SLC1A5 protein expression were strongly correlated in luminal B, HER2 + and triple-negative BC (TNBC). Both high SLC1A5 mRNA and SLC1A5 protein expression were associated with larger tumour size, higher grade, and positive axillary lymph node metastases (P < 0.01). Importantly, high SLC1A5 expression correlated with poor BC-specific survival specifically in the highly proliferative luminal subtype (P < 0.001). Furthermore, SLC1A5 knockdown by siRNA or GPNA inhibition significantly reduced cell proliferation and glutamine uptake in ZR-75-1 cells. Our findings suggest SLC1A5 plays a key role in the aggressive luminal BC subtype and represents a potential therapeutic target. Further research is needed to explore SLC1A5 function in luminal BC and its association with Gln metabolism pathways.

Citation

Alfarsi, L. H., El Ansari, R., Erkan, B., Fakroun, A., Craze, M. L., Aleskandarany, M. A., Cheng, K. W., Ellis, I. O., Rakha, E. A., & Green, A. R. (2025). SLC1A5 is a Key Regulator of Glutamine Metabolism and a Prognostic Marker for Aggressive Luminal Breast Cancer. Scientific Reports, 15, Article 2805. https://doi.org/10.1038/s41598-025-87292-1

Journal Article Type Article
Acceptance Date Jan 17, 2025
Online Publication Date Jan 22, 2025
Publication Date Jan 22, 2025
Deposit Date Jan 17, 2025
Publicly Available Date Jan 27, 2025
Journal Scientific Reports
Electronic ISSN 2045-2322
Publisher Nature Publishing Group
Peer Reviewed Peer Reviewed
Volume 15
Article Number 2805
DOI https://doi.org/10.1038/s41598-025-87292-1
Keywords SLC1A5, breast cancer, prognosis, tumour marker
Public URL https://nottingham-repository.worktribe.com/output/44232339
Publisher URL https://www.nature.com/articles/s41598-025-87292-1

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