Abstract
We investigated the diagnostic and prognostic potential of serum N-glycan profiling for castration-resistant prostate cancer (CRPC). We retrospectively investigated serum N-glycan structural analysis by glycoblotting for 287 patients with benign prostatic hyperplasia (BPH), 289 patients with newly diagnosed prostate cancer (PC), 57 patients with PC treated with androgen-deprivation therapy without disease progression (PC-ADT), and 60 patients with CRPC. N-Glycan profiling was compared between the non-CRPC (BPH, newly diagnosed PC and PC-ADT) and CRPC patients. We obtained the quantitative score for CRPC (CRPC N-glycan score) by discriminant analysis based on the combination of 9 N-glycans that were significantly associated with CRPC. The median CRPC N-glycan score was found to be significantly greater in CRPC patients than in non-CRPC patients. The CRPC N-glycan score could classify CRPC patients with sensitivity, specificity, and area under the curve of 87%, 69%, and 0.88, respectively. The CRPC N-glycan score >1.7 points was significantly associated with poor prognosis in patients with CRPC. The glycoprotein analysis showed that not immunoglobulins but α-1-acid glycoprotein (AGP) were a potential candidate for the carrier protein of N-glycans. The overexpression of specific N-glycans may be associated with their castration-resistant status and be a potential biomarker for CRPC.
Highlights
We investigated the diagnostic and prognostic potential of serum N-glycan profiling for castrationresistant prostate cancer (CRPC)
The age of patients in the benign prostatic hyperplasia (BPH) group was younger than that in the newly diagnosed PC, PC treated with androgen-deprivation therapy without disease progression (PC-ADT) and CRPC groups
We evaluated the diagnostic and prognostic potentials of serum N-glycan profiling for CRPC using high-throughput, comprehensive, and quantitative N-glycomics that have a potential to distinguish CRPC
Summary
We investigated the diagnostic and prognostic potential of serum N-glycan profiling for castrationresistant prostate cancer (CRPC). The overexpression of specific N-glycans may be associated with their castration-resistant status and be a potential biomarker for CRPC. Our previous studies suggested that a quantitative N-glycan analysis is a promising approach for biomarker screening in several cancers[14,21,27,28,29,30]. Among these studies, a few evaluated the potential diagnostic value of serum N-glycomics (tri- and tetra-antennary N-glycans) in patients with CRPC14,21,30. We evaluated the diagnostic and prognostic potential of serum N-glycan profiling for CRPC using a combination of serum N-glycans
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