Shen Li, Dong Xiaoxia, Yu Meiyun, Luo Zhiguo, Wu Shiliang
Department of Clinical Oncology, Taihe Hospital, Hubei University of Medicine, Shiyan 442000, Hubei, China; Department of Biochemistry and Molecular Biology, Soochow University, Suzhou 215123, Jiangsu, China.
Department of pharmacology, School of Basic Medicine, Hubei University of Medicine, Shiyan 442000, Hubei, China.
J Cancer. 2017 Feb 5;8(2):314-322. doi: 10.7150/jca.16526. eCollection 2017.
β1, 3-N-acetylglucosminyltransferase 8(β3GnT8) synthesizes a unique cabohydrate structure known as polylactosamine, and plays a vital role in progression of various human cancer types. However, its involvement in gastric cancer remains unclear. In this study, we analyzed the expression and clinical significance of β3GnT8 by Western blot in 6 paired fresh gastric cancer tissues, noncancerous tissues and immunohistochemistry on 110 paraffin-embedded slices. β3GnT8 was found to be over-expressed in gastric cancer tissues, which correlated with lymph node metastasis and TNM stage. Forced the expression of β3GnT8 promoted migration and invasion of gastric cancer cells, whereas β3GnT8 knockdown led to the opposite results. Further studies showed that the regulated β3GnT8 could convert the heterogeneous N-glycosylated forms of CD147 and change the polylactosamine structures carried on CD147. In addition, our data suggested the annexin A2 (ANXA2) to be an essential interaction partner of β3GnT8 during the process of CD147 glycosylation. Collectively, these results provide a novel molecular mechanism for β3GnT8 in promotion of gastric cancer invasion and metastasis. Targeting β3GnT8 could serve as a new strategy for future gastric cancer therapy.
β1,3-N-乙酰氨基葡萄糖转移酶8(β3GnT8)可合成一种名为多乳糖胺的独特碳水化合物结构,在多种人类癌症类型的进展中发挥着至关重要的作用。然而,其在胃癌中的作用仍不清楚。在本研究中,我们通过蛋白质免疫印迹法分析了6对新鲜胃癌组织和癌旁组织中β3GnT8的表达及临床意义,并对110张石蜡包埋切片进行了免疫组织化学分析。结果发现β3GnT8在胃癌组织中过表达,且与淋巴结转移和TNM分期相关。过表达β3GnT8可促进胃癌细胞的迁移和侵袭,而敲低β3GnT8则导致相反的结果。进一步研究表明,β3GnT8的调控可改变CD147的异质性N-糖基化形式,并改变CD147上携带的多乳糖胺结构。此外,我们的数据表明膜联蛋白A2(ANXA2)是β3GnT8在CD147糖基化过程中的重要相互作用伙伴。总之,这些结果为β3GnT8促进胃癌侵袭和转移提供了一种新的分子机制。靶向β3GnT8可能成为未来胃癌治疗的新策略。