Expression of Fucosyltransferase 8 Is Associated with an Unfavorable Clinical Outcome in Non-Small Cell Lung Cancers

被引:58
作者
Honma, Rio [1 ]
Kinoshita, Ichiro [1 ]
Miyoshi, Eiji [5 ]
Tomaru, Utano [2 ]
Matsuno, Yoshihiro [4 ]
Shimizu, Yasushi [1 ]
Takeuchi, Satoshi [1 ]
Kobayashi, Yuka [6 ]
Kaga, Kichizo [3 ]
Taniguchi, Naoyuki [7 ]
Dosaka-Akita, Hirotoshi [1 ]
机构
[1] Hokkaido Univ, Grad Sch Med, Dept Med Oncol, Sapporo, Hokkaido 0608638, Japan
[2] Hokkaido Univ, Grad Sch Med, Dept Pathol, Sapporo, Hokkaido 0608638, Japan
[3] Hokkaido Univ, Grad Sch Med, Dept Cardiovasc & Thorac Surg, Sapporo, Hokkaido 0608638, Japan
[4] Hokkaido Univ Hosp, Dept Surg Pathol, Sapporo, Hokkaido 060, Japan
[5] Osaka Univ, Grad Sch Med, Dept Mol Biochem & Clin Invest, Suita, Osaka, Japan
[6] J Oil Mills Inc, Yokohama, Kanagawa, Japan
[7] RIKEN, Max Planck Joint Res Ctr, Riken Global Res Cluster, Syst Glycobiol Res Grp, Wako, Saitama, Japan
关键词
Fucosyltransferase; 8; Non-small cell lung cancers; Prognosis; Histology; N-ACETYLGLUCOSAMINYLTRANSFERASE-V; HEPATOCELLULAR-CARCINOMA; ALPHA(1,6)FUCOSYLTRANSFERASE; IDENTIFICATION; PROGNOSIS; ENZYME; ROLES;
D O I
10.1159/000369495
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objecitive: Fucosyltransferase 8 (FUT8), the only enzyme responsible for the core alpha 1,6-fucosylation of asparagine-linked oligosaccharides of glycoproteins, is a vital enzyme in cancer development and progression. We examined FUT8 expression in non-small cell lung cancers (NSCLCs) to analyze its clinical significance. We also examined the expression of guanosine diphosphate-mannose-4,6-dehydratase (GMD), which is imperative for the synthesis of fucosylated oligosaccharides. Methods: Using immunohistochemistry, we evaluated the expression of FUT8 and GMD in relation to patient survival and prognosis in potentially curatively resected NSCLCs. Results: High expression of FUT8 was found in 67 of 129 NSCLCs (51.9%) and was significantly found in non-squamous cell carcinomas (p = 0.008). High expression of FUT8 was associated with poor survival (p = 0.03) and was also a significant and independent unfavorable prognostic factor in patients with potentially curatively resected NSCLCs (p = 0.047). High expression of GMD was significantly associated with high FUT8 expression (p = 0.04). Conclusions: High expression of FUT8 is associated with an unfavorable clinical outcome in patients with potentially curatively resected NSCLCs, suggesting that FUT8 can be a prognostic factor. The analysis of FUT8 expression and its core fucosylated products may provide new insights for the therapeutic targets of NSCLCs. (C) 2015 S. Karger AG, Basel
引用
收藏
页码:298 / 308
页数:11
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