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Serum N-glycan profiling is a potential biomarker for castration-resistant prostate cancer

Authors :
Hiroyuki Ito
Chikara Ohyama
Shin-Ichiro Nishimura
Yusuke Ishibashi
Tohru Yoneyama
Hayato Yamamoto
Yuki Tobisawa
Yasuhiro Hashimoto
Takahiro Yoneyama
Shingo Hatakeyama
Teppei Matsumoto
Source :
Scientific Reports, Vol 9, Iss 1, Pp 1-8 (2019), Scientific Reports
Publication Year :
2019
Publisher :
Nature Publishing Group, 2019.

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.

Details

Language :
English
ISSN :
20452322
Volume :
9
Issue :
1
Database :
OpenAIRE
Journal :
Scientific Reports
Accession number :
edsair.doi.dedup.....7b81c61d2a3ae004476d024425e3c61e
Full Text :
https://doi.org/10.1038/s41598-019-53384-y