Serum N-glycan profiling is a potential biomarker for castration-resistant prostate cancer.
Aged
Aged, 80 and over
Area Under Curve
Biomarkers, Tumor
/ blood
Case-Control Studies
Discriminant Analysis
Humans
Male
Middle Aged
Polysaccharides
/ blood
Prognosis
Prostatic Hyperplasia
/ metabolism
Prostatic Neoplasms, Castration-Resistant
/ diagnosis
Retrospective Studies
Sensitivity and Specificity
Journal
Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288
Informations de publication
Date de publication:
14 11 2019
14 11 2019
Historique:
received:
12
07
2019
accepted:
31
10
2019
entrez:
16
11
2019
pubmed:
16
11
2019
medline:
3
11
2020
Statut:
epublish
Résumé
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.
Identifiants
pubmed: 31727974
doi: 10.1038/s41598-019-53384-y
pii: 10.1038/s41598-019-53384-y
pmc: PMC6856113
doi:
Substances chimiques
Biomarkers, Tumor
0
Polysaccharides
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
16761Références
Cancer Med. 2017 Apr;6(4):739-748
pubmed: 28317343
Front Oncol. 2018 Jan 15;7:328
pubmed: 29379771
Anticancer Res. 2008 Jul-Aug;28(4A):1993-9
pubmed: 18649738
BMJ. 2018 Sep 5;362:k3519
pubmed: 30185521
Am J Cancer Res. 2016 Nov 01;6(11):2390-2415
pubmed: 27904760
Int J Clin Oncol. 2017 Apr;22(2):214-221
pubmed: 27730440
World J Gastroenterol. 2018 Jun 28;24(24):2537-2554
pubmed: 29962812
Int J Urol. 2019 Oct;26(10):956-970
pubmed: 31183923
Cells. 2019 Aug 13;8(8):
pubmed: 31412618
J Proteome Res. 2007 May;6(5):1822-32
pubmed: 17432893
Sci Rep. 2019 Aug 19;9(1):12071
pubmed: 31427687
Prostate. 2014 Nov;74(15):1521-9
pubmed: 25154914
Int J Urol. 2019 Aug;26(8):827-832
pubmed: 31183899
Sci Rep. 2019 Mar 11;9(1):4030
pubmed: 30858508
Int J Urol. 2018 Jun;25(6):524-531
pubmed: 29740894
Anticancer Res. 2019 Jul;39(7):3373-3378
pubmed: 31262858
Electrophoresis. 2018 Apr;39(7):998-1005
pubmed: 29330871
Cancer Sci. 2019 Aug;110(8):2573-2589
pubmed: 31145522
FEBS Lett. 2019 Nov;593(21):2966-2976
pubmed: 31509238
World J Urol. 2019 Sep;37(9):1827-1835
pubmed: 30511214
Cancer Cell. 2019 Jul 8;36(1):6-16
pubmed: 31287993
Int J Urol. 2017 Apr;24(4):272-278
pubmed: 28253548
J Urol. 2014 Mar;191(3):805-13
pubmed: 24140550
Mol Cell Proteomics. 2008 Feb;7(2):370-7
pubmed: 17986439
Curr Protein Pept Sci. 2007 Feb;8(1):91-108
pubmed: 17305563
Clin Transl Oncol. 2020 Jul;22(7):1033-1039
pubmed: 31617061
Front Immunol. 2019 Sep 06;10:2120
pubmed: 31552050
Glycoconj J. 2018 Apr;35(2):139-160
pubmed: 29680984
Eur Urol Focus. 2018 Apr;4(3):405-411
pubmed: 28753809
Int J Urol. 2018 Mar;25(3):220-231
pubmed: 29266472
Int J Urol. 2018 Apr;25(4):345-351
pubmed: 29396873
Eur Urol Oncol. 2019 May;2(3):320-328
pubmed: 31200847
Clin Chim Acta. 2019 Nov;498:52-61
pubmed: 31400314