Serum N-glycan profiles in patients with intraductal papillary mucinous neoplasms of the pancreas

被引:13
作者
Akimoto, Yutaka [1 ]
Nouso, Kazuhiro [1 ]
Kato, Hironari [1 ]
Miyahara, Koji [1 ]
Dohi, Chihiro [1 ]
Morimoto, Yuki [1 ]
Kinugasa, Hideaki [1 ]
Tomoda, Takeshi [1 ]
Yamamoto, Naoki [1 ]
Tsutsumi, Koichiro [1 ]
Kuwaki, Kenji [1 ]
Onishi, Hideki [1 ]
Ikeda, Fusao [1 ]
Nakamura, Shinichiro [1 ]
Shiraha, Hidenori [1 ]
Takaki, Akinobu [1 ]
Okada, Hiroyuki [1 ,2 ]
Amano, Maho [3 ,4 ,5 ]
Nishimura, Shin-Ichiro [3 ,4 ,5 ]
Yamamoto, Kazuhide [1 ]
机构
[1] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Gastroenterol & Hepatol, Kita Ku, Okayama, Okayama 7008558, Japan
[2] Okayama Univ Hosp, Dept Endoscopy, Okayama, Japan
[3] Hokkaido Univ, Fac Adv Life Sci, Field Drug Discovery Res, Sapporo, Hokkaido, Japan
[4] Hokkaido Univ, Grad Sch Life Sci, Sapporo, Hokkaido, Japan
[5] Med Chem Pharmaceut Co Ltd, Sapporo, Hokkaido, Japan
基金
日本学术振兴会;
关键词
Biological markers; Fucosylation; Glycomics; Intraductal papillary mucinous neoplasm; Pancreas; Malignancy; INTERNATIONAL CONSENSUS GUIDELINES; FUCOSYLATED HAPTOGLOBIN; HEPATOCELLULAR-CARCINOMA; PROGNOSTIC MARKER; CYST FLUID; CANCER; MALIGNANCY; MANAGEMENT; CYTOLOGY; IDENTIFICATION;
D O I
10.1016/j.pan.2015.05.470
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/objectives: Diagnosing the invasiveness of intraductal papillary mucinous neoplasms (IPMNs) is difficult, especially by blood test. Alterations in serum glycan profiles have been reported for several cancers, but changes in serum glycan profiles have not been investigated in patients with IPMNs. The objectives of this study were to determine the serum N-glycan profile and to investigate its clinical utility in patients with IPMNs. Methods: We measured serum N-glycan profiles in 79 patients with IPMNs, including 13 invasive IPMNs, by performing comprehensive glycome analysis and assessed the relationship between N-glycan changes and clinical parameters. Results: Seventy glycans were identified and their expression profiles were significantly different depending on the cyst size, the presence of an enhancing solid component, and the histological grade of the IPMN. Nine glycans were highly expressed in patients with invasive IPMNs. The glycan m/z 3195, which is a fucosylated tri-antennary glycan, had the highest diagnostic value for distinguishing invasive IPMNs from non-invasive IPMNs (area under the receiver operating characteristic curve = 0.803). Multivariate analyses revealed high levels of m/z 3195 [odds ratio (OR), 20.5; 95% confidence interval (CI) 2.60-486.4] and the presence of enhancing solid components (OR, 35.8; 95% Cl, 5.39-409.6) were significant risk factors for invasive IPMNs. Conclusions: We performed a comprehensive evaluation of the changes in serum N-glycan profiles in patients with IPMNs for the first time. We determined that increased expression of fucosylated complex-type glycans, especially m/z 3195, is a potential marker for invasive IPMNs. Copyright (C) 2015, IAP and EPC. Published by Elsevier India, a division of Reed Elsevier India Pvt. Ltd. All rights reserved.
引用
收藏
页码:432 / 438
页数:7
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