Serum N-glycan profiling is a potential biomarker for castration-resistant prostate cancer
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...
Saved in:
Published in | Scientific reports Vol. 9; no. 1; pp. 16761 - 8 |
---|---|
Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
14.11.2019
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | 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. |
---|---|
ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/s41598-019-53384-y |