Akademik Veri Yönetim Sistemi
MOLECULAR GENETICS AND GENOMICS, cilt.301, sa.1, 2026 (SCI-Expanded, Scopus)
Liver-associated alterations are increasingly recognized as critical contributors to breast cancer progression and systemic disease burden, yet the molecular mechanisms underlying these changes remain poorly understood. In particular, aberrant protein glycosylation has emerged as a key regulator of cancer-associated tissue remodeling and inter-organ communication. In this study, we investigated whether glycosylation-related gene expression and glycoprotein signatures in liver tissue could serve as biomarkers of breast cancer-associated hepatic alterations. We developed a medium-throughput quantitative real-time reverse transcriptase-PCR array targeting genes encoding glycosyltransferases and glycosylhydrolases involved in glycan synthesis, modification, and catabolism. This approach enabled a systematic analysis of over 134 glycosylation-related genes and facilitated direct integration of transcriptomic data with glycan structural profiles in the liver tissue of breast tumor-bearing mice. Our analysis revealed significant upregulation of Galntl2, GNE, and Manea, accompanied by increased sialic acid levels in both liver and circulating blood. Receiver operating characteristic (ROC) analysis demonstrated that these genes exhibit excellent diagnostic performance in liver tissue, achieving 100% sensitivity and specificity. Collectively, these findings highlight glycosylation-related gene signatures as robust indicators of breast cancer-associated liver alterations and suggest that dysregulated hepatic glycosylation represents a biologically meaningful axis linking tumor progression with systemic metabolic and glycomic remodeling. This work provides a framework for exploring glycosylation-based biomarkers and therapeutic targets in cancer-associated organ dysfunction.