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大鼠肝脏和肝癌中负责糖蛋白和神经节苷脂糖链形成的唾液酸转移酶水平的比较研究。

Comparative study of the levels of sialyltransferases responsible for the formation of sugar chains in glycoproteins and gangliosides in rat liver and hepatomas.

作者信息

Miyagi T, Koseki M, Tsuiki S

机构信息

Research Institute for Tuberculosis and Cancer, Tohoku University, Sendai.

出版信息

Jpn J Cancer Res. 1988 Jun;79(6):742-9. doi: 10.1111/j.1349-7006.1988.tb02231.x.

Abstract

Sialyltransferases responsible for the formation of sugar chains in glycoproteins were studied in rat hepatoma in comparison with rat liver. Hepatoma induced by feeding Wistar rats with 3'-methyl-4-dimethylaminoazobenzene (MeDAB) was more active than Wistar liver in sialylating asialo-orosomucoid, and this was due to an increased activity of Gal(beta 1----4)GlcNAc (alpha 2----6) sialyltransferase, the major sialyltransferase in these tissues. Gal(beta 1----3,4)GlcNAc (alpha 2----3) sialyltransferase and the sialyltransferase acting on asialo-bovine submaxillary mucin were, however, decreased in the hepatoma. A similar pattern of sialyltransferase alterations was observed in regenerating liver and other tumors such as AH-109A hepatoma and Sato lung cancer, both of which had been inoculated into Donryu rats. In contrast to these sialyltransferases, the activities of the sialyltransferases responsible for the formation of gangliosides were markedly different even between Wistar and Donryu livers. When compared with Wistar liver, MeDAB-induced hepatoma was higher in lactosylceramide- and lower in GM3-sialyltransferase activity, but these two activities were both lower in AH-109A compared with Donryu liver.

摘要

与大鼠肝脏相比,研究了大鼠肝癌中负责糖蛋白糖链形成的唾液酸转移酶。用3'-甲基-4-二甲基氨基偶氮苯(MeDAB)喂养Wistar大鼠诱导的肝癌在唾液酸化去唾液酸血清类黏蛋白方面比Wistar肝脏更活跃,这是由于Gal(β1→4)GlcNAc(α2→6)唾液酸转移酶(这些组织中的主要唾液酸转移酶)活性增加所致。然而,Gal(β1→3,4)GlcNAc(α2→3)唾液酸转移酶和作用于去唾液酸牛颌下黏蛋白的唾液酸转移酶在肝癌中减少。在再生肝脏以及接种到Donryu大鼠体内的其他肿瘤(如AH-109A肝癌和佐藤肺癌)中也观察到了类似的唾液酸转移酶变化模式。与这些唾液酸转移酶不同,即使在Wistar和Donryu肝脏之间,负责神经节苷脂形成的唾液酸转移酶的活性也明显不同。与Wistar肝脏相比,MeDAB诱导的肝癌中乳糖基神经酰胺唾液酸转移酶活性较高,GM3唾液酸转移酶活性较低,但与Donryu肝脏相比,AH-109A中的这两种活性均较低。

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