Background: Breast cancer (BrCa) is the most prevalent tumor among women globally, aside from nonmelanoma skin malignancies. Unfortunately, many BrCa patients exhibit a poor response to immune checkpoint inhibitors (ICIs) because of a deficiency of infiltrating immune cells. Earlier research has shown that guanylate-binding protein 1 (GBP1) can modify the inhibitory properties of inflammatory cytokines on endothelial cell proliferation, immigration, and invasion.
Objective: Since the fundamental functions of the GBP family in the cancer-immune cycle is uncertain, according to recent findings, the function of GBPs in BrCa was studied. However, the underlying function of the GBP family in the cancer-immunity cycle is uncertain. We decided to study GBPs’ role in BrCa.
Methods: We applied GEPIA, UALCAN, cBioPortal, GeneMANIA, Kaplan-Meier plotter, Human Protein Atlas, STRING, and TIMER in our analysis.
Results: Our results confirmed a strong relation between the expression of GBP1/GBP2/GBP3/GBP4/GBP5/GBP6/GBP7 and the infiltration of all immune cells. Specifically, high GBP1/4/5 expression was strongly linked with increased infiltration of dendritic cells, B cells, CD4+ T cells, CD8+ T cells, and neutrophils in BrCa, whereas GBP2/3/6/7 expression showed a weaker positive correlation.
Conclusion: These results suggest a therapeutic assessment for the GBP family in combination with ICIs for treating BrCa.