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A comprehensive analysis of the diagnostic and prognostic value associated with the SLC7A family members in breast cancer

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GLAND SURGERY
卷 11, 期 2, 页码 389-411

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AME PUBLISHING COMPANY
DOI: 10.21037/gs-21-909

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Breast cancer (BC); solute carrier family 7; biomarker; prognosis; immune infiltration

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This study investigated the expression and prognostic value of SLC7 family genes in breast cancer. The results revealed that high SLC7A5 expression was associated with poorer survival time, while SLC7A4 was associated with good progression-free interval and disease-specific survival. SLC7A3 expression was positively associated with overall survival and distant metastasis-free survival. SLC7A family genes were strongly correlated with T helper cells and natural killer cells, suggesting their role in modulating immune infiltration in breast cancer.
Background: The solute carrier (SLC) 7 family genes play central roles in cancer cell metabolism as glucose and glutamate transporters. However, their expression and prognostic value in breast cancer (BC) remains to be elucidated. Methods: Clinical data from BC patients were downloaded from The Cancer Genome Atlas (TCGA) and the Kaplan-Meier (KM) plotter database. The mechanisms underlying the association between SLC7A expression and overall survival (OS) were explored using Cox regression and log-rank tests. ESTIMATE gives a measure of the immune-cell infiltrates. Single-sample (ss) Gene Set Enrichment Analysis (GSEA) was conducted to quantify immune cell infiltration. Results: High SLC7A5 expression was associated with a poorer survival time in BC patients according to the TCGA and KM plotter data. SLC7A4 was associated with good progression-free interval (PFI) and disease-specific survival (DSS) according to the TCGA data. Furthermore, SLC7A4 was correlated with good prognosis of OS, distant metastasis-free survival (DMFS), relapse-free survival (RFS), and post-progression survival (PPS) according to the KM plotter data. SLC7A3 expression was positively associated with OS, but was not strongly associated with PFI nor DSS in the TCGA data. However, SLC7A3 was positively correlated with DMFS and RFS in the KM database analysis. SLC7A had excellent diagnostic value in BC patients and was strongly correlated with tumor infiltration. T helper 2 (Th2) cells, CD56 bright natural killer (NK) cells, and NK cells were the most strongly correlated with the SLC7A family genes, suggesting that these genes play a crucial role in BC partly by modulating immune infiltration. Conclusions: SLC7A4 and SLC7A5 expression levels may be sensitive biomarkers for predicting BC outcomes. SLC7A3 may be a potential diagnostic and prognostic biomarker in BC, but further studies are warranted to verify these results.

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