Akihiro Deguchi, S. Hitoshi, Takeshi Yoshimura, I. Fujimoto, T. Ikeda, A. Ishii, Mikito Higashi, T. Masaki, S. Kuriyama, K. Ikenaka
{"title":"GnT v催化的n -聚糖产物在肝癌中不增加","authors":"Akihiro Deguchi, S. Hitoshi, Takeshi Yoshimura, I. Fujimoto, T. Ikeda, A. Ishii, Mikito Higashi, T. Masaki, S. Kuriyama, K. Ikenaka","doi":"10.4172/2153-0637.S5-003","DOIUrl":null,"url":null,"abstract":"Sugar chains envelop the vast majority of the cell surface and thus have been considered to play pivotal roles in cell-to-cell and cell-to-extracellular matrix interactions. Recent studies have shown that expression of N-acetylglucosaminyltransferase (GnT) V is induced in hepatomas, and high-branched N-linked sugar chains play important roles in carcinogenesis and metastasis. However, the precise structural changes have not yet been studied in detail. Here, we compared sugar chains expressed in normal mouse liver, regenerating liver, three mouse hepatoma cell lines and Hepa 1-6-related tumors obtained by inoculation of Hepa 1-6 cells into liver or subcutaneous tissue of BALB/c nu/nu mice. The products of GnT V were found to be present in similar proportions in the mouse liver and in hepatomas, while there was a big difference in the amount of GnT IV products in these organs. Normal mouse liver and regenerating mouse liver contained small amounts of sugar chains produced by the action of GnT IV, while such chains were abundant in hepatoma cell lines and in Hepa 1-6-related tumors. Analysis of N-linked sugar chains in human livers and in hepatocellular carcinoma (HCC) revealed that both GnT IV and GnT V products are present in human liver, but their total content did not change during malignant transformation. Thus there was no increase in GnT V N-glycan products in hepatoma tissues in the mouse model or in humans.","PeriodicalId":89585,"journal":{"name":"Journal of glycomics & lipidomics","volume":"2012 1","pages":"1-6"},"PeriodicalIF":0.0000,"publicationDate":"2013-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"GnT V-Catalyzed N-glycan Products are not increased in Hepatomas\",\"authors\":\"Akihiro Deguchi, S. Hitoshi, Takeshi Yoshimura, I. Fujimoto, T. Ikeda, A. Ishii, Mikito Higashi, T. Masaki, S. Kuriyama, K. Ikenaka\",\"doi\":\"10.4172/2153-0637.S5-003\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Sugar chains envelop the vast majority of the cell surface and thus have been considered to play pivotal roles in cell-to-cell and cell-to-extracellular matrix interactions. Recent studies have shown that expression of N-acetylglucosaminyltransferase (GnT) V is induced in hepatomas, and high-branched N-linked sugar chains play important roles in carcinogenesis and metastasis. However, the precise structural changes have not yet been studied in detail. Here, we compared sugar chains expressed in normal mouse liver, regenerating liver, three mouse hepatoma cell lines and Hepa 1-6-related tumors obtained by inoculation of Hepa 1-6 cells into liver or subcutaneous tissue of BALB/c nu/nu mice. The products of GnT V were found to be present in similar proportions in the mouse liver and in hepatomas, while there was a big difference in the amount of GnT IV products in these organs. Normal mouse liver and regenerating mouse liver contained small amounts of sugar chains produced by the action of GnT IV, while such chains were abundant in hepatoma cell lines and in Hepa 1-6-related tumors. Analysis of N-linked sugar chains in human livers and in hepatocellular carcinoma (HCC) revealed that both GnT IV and GnT V products are present in human liver, but their total content did not change during malignant transformation. Thus there was no increase in GnT V N-glycan products in hepatoma tissues in the mouse model or in humans.\",\"PeriodicalId\":89585,\"journal\":{\"name\":\"Journal of glycomics & lipidomics\",\"volume\":\"2012 1\",\"pages\":\"1-6\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2013-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of glycomics & lipidomics\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4172/2153-0637.S5-003\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of glycomics & lipidomics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4172/2153-0637.S5-003","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
摘要
糖链包裹着绝大多数细胞表面,因此被认为在细胞间和细胞外基质相互作用中起着关键作用。最近的研究表明,n -乙酰氨基葡萄糖转移酶(GnT) V在肝癌中被诱导表达,高支链的n -糖链在癌变和转移中起重要作用。然而,精确的结构变化尚未被详细研究。在此,我们比较了正常小鼠肝脏、再生肝脏、三种小鼠肝癌细胞系中表达的糖链,以及通过将Hepa 1-6细胞接种到BALB/c nu/nu小鼠肝脏或皮下组织中获得的Hepa 1-6相关肿瘤。GnT - V产物在小鼠肝脏和肝癌中以相似的比例存在,而在这些器官中GnT - IV产物的量有很大差异。正常小鼠肝脏和再生小鼠肝脏中含有少量由GnT IV作用产生的糖链,而肝癌细胞系和Hepa 1-6相关肿瘤中含有大量糖链。对人类肝脏和肝细胞癌(HCC)中n -链糖链的分析表明,GnT IV和GnT V产物都存在于人类肝脏中,但它们的总含量在恶性转化过程中没有变化。因此,在小鼠模型或人类肝癌组织中,GnT V n -聚糖产物没有增加。
GnT V-Catalyzed N-glycan Products are not increased in Hepatomas
Sugar chains envelop the vast majority of the cell surface and thus have been considered to play pivotal roles in cell-to-cell and cell-to-extracellular matrix interactions. Recent studies have shown that expression of N-acetylglucosaminyltransferase (GnT) V is induced in hepatomas, and high-branched N-linked sugar chains play important roles in carcinogenesis and metastasis. However, the precise structural changes have not yet been studied in detail. Here, we compared sugar chains expressed in normal mouse liver, regenerating liver, three mouse hepatoma cell lines and Hepa 1-6-related tumors obtained by inoculation of Hepa 1-6 cells into liver or subcutaneous tissue of BALB/c nu/nu mice. The products of GnT V were found to be present in similar proportions in the mouse liver and in hepatomas, while there was a big difference in the amount of GnT IV products in these organs. Normal mouse liver and regenerating mouse liver contained small amounts of sugar chains produced by the action of GnT IV, while such chains were abundant in hepatoma cell lines and in Hepa 1-6-related tumors. Analysis of N-linked sugar chains in human livers and in hepatocellular carcinoma (HCC) revealed that both GnT IV and GnT V products are present in human liver, but their total content did not change during malignant transformation. Thus there was no increase in GnT V N-glycan products in hepatoma tissues in the mouse model or in humans.