Author:
Tanaka-Okamoto Miki,Hanzawa Ken,Murakami Hiroko,Mukai Mikio,Takahashi Hidenori,Omori Takeshi,Ikezawa Kenji,Ohkawa Kazuyoshi,Ohue Masayuki,Miyamoto Yasuhide
Abstract
AbstractUrinary free-glycans are promising markers of disease. In this study, we attempted to identify novel tumor markers by focusing on neutral free-glycans in urine. Free-glycans extracted from the urine of normal subjects and cancer patients with gastric, colorectal, pancreatic and bile duct were fluorescently labeled with 2-aminopyridine. Profiles of these neutral free-glycans constructed using multidimensional high performance liquid chromatography separation were compared between normal controls and cancer patients. The analysis identified one glycan in the urine of cancer patients with a unique structure, which included a pentose residue. To reveal the glycan structure, the linkage fashion, monosaccharide species and enantiomer of the pentose were analyzed by high performance liquid chromatography and mass spectrometry combined with several chemical treatments. The backbone of the glycan was a monoantennary complex-type free-N-glycan containing β1,4-branch. The pentose residue was attached to the antennal GlcNAc and released by α1,3/4-l-fucosidase. Intriguingly, the pentose residue was consistent with d-arabinose. Collectively, this glycan structure was determined to be Galβ1-4(d-Araβ1-3)GlcNAcβ1-4Manα1-3Manβ1-4GlcNAc-PA. Elevation of d-arabinose-containing free-glycans in the urine of cancer patients was confirmed by selected reaction monitoring. This is the first study to unequivocally show the occurrence of a d-arabinose-containing oligosaccharide in human together with its detailed structure.
Funder
Japan Society for the Promotion of Science
Osaka foundation for the prevention of cancer and cardiovascular diseases
Publisher
Springer Science and Business Media LLC
Reference41 articles.
1. Varki, A. Biological roles of glycans. Glycobiology 27, 3–49. https://doi.org/10.1093/glycob/cww086 (2017).
2. Parodi, A., Cummings, R. D. & Aebi, M. in Essentials of glycobiology (eds A. Varki et al.) 503–511 (Cold Spring Harbor Laboratory Press Copyright 2015–2017 by The Consortium of Glycobiology Editors, La Jolla, California. All rights reserved., 2015).
3. Moremen, K. W., Tiemeyer, M. & Nairn, A. V. Vertebrate protein glycosylation: diversity, synthesis and function. Nat. Rev. Mol. Cell Biol. 13, 448–462. https://doi.org/10.1038/nrm3383 (2012).
4. Ohashi, S., Iwai, K., Mega, T. & Hase, S. Quantitation and isomeric structure analysis of free oligosaccharides present in the cytosol fraction of mouse liver: detection of a free disialobiantennary oligosaccharide and glucosylated oligomannosides. J. Biochem. 126, 852–858. https://doi.org/10.1093/oxfordjournals.jbchem.a022526 (1999).
5. Ishizuka, A. et al. Accumulation of free complex-type N-glycans in MKN7 and MKN45 stomach cancer cells. Biochem. J. 413, 227–237. https://doi.org/10.1042/bj20071562 (2008).
Cited by
5 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献