Wisteria floribunda agglutinin-positive mucin 1 is a sensitive biliary marker for human cholangiocarcinoma

粘蛋白 MUC1号 肝病学 染色 病理 胆管 单克隆抗体 凝集素 医学 免疫组织化学 内科学 胃肠病学 生物 抗体 分子生物学 凝集素 免疫学
作者
Atsushi Matsuda,Atsushi Kuno,Toru Kawamoto,Hideki Matsuzaki,Tatsuro Irimura,Yuzuru Ikehara,Yoh Zen,Yasuni Nakanuma,Masakazu Yamamoto,Nobuhiro Ohkohchi,Junichi Shoda,Jun Hirabayashi,Hisashi Narimatsu
出处
期刊:Hepatology [Lippincott Williams & Wilkins]
卷期号:52 (1): 174-182 被引量:93
标识
DOI:10.1002/hep.23654
摘要

Cholangiocarcinoma (CC) is an aggressive malignant tumor for which useful markers are not presently available for early and precise diagnosis. The aim of this study was therefore to identify a high-performance diagnostic marker with a special focus on glyco-alteration of glycoproteins. In the course of study, we found that Wisteria floribunda agglutinin (WFA) is the best probe to differentiate intrahepatic cholangiocarcinoma (ICC) lesions from normal bile duct epithelia (BDE) ( P < 0.0001). The subsequent histochemical study confirmed ICC-specific WFA staining on 165 tissue specimens. On the other hand, the WFA staining was shown to be closely associated with that of MY.1E12 established previously against sialylated mucin 1 (MUC1) by double-staining experiments. Moreover, glyco-alteration of MUC1 could be verified by western blotting of WFA-captured bile samples from patients with CC patients. Thus, we attempted to construct an enzyme-linked immunosorbent assay system for more convenient CC diagnosis, where WFA-coated plates, the specific monoclonal antibody MY.1E12, and the bile specimens from CC including ICC (n = 30) and benign diseases (n = 38) were combined. As a result, CC was clearly distinguished from benign diseases with statistical scores (sensitivity = 90.0%, specificity = 76.3%, and area under the curve = 0.85). As a particular note, the obtained sensitivity is the highest score among those having been so far reported. Conclusion: Our approach focusing significant glyco-alteration of a particular glycoprotein yielded a novel diagnostic system for CC with satisfactory clinical scores. Hepatology 2010
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