Suppr超能文献

人结直肠癌中癌特异性荆豆凝集素-I结合糖蛋白及其与癌胚抗原的关系

Carcinoma-specific Ulex europaeus agglutinin-I binding glycoproteins of human colorectal carcinoma and its relation to carcinoembryonic antigen.

作者信息

Matsushita Y, Yonezawa S, Nakamura T, Shimizu S, Ozawa M, Muramatsu T, Sato E

出版信息

J Natl Cancer Inst. 1985 Aug;75(2):219-26.

PMID:3894751
Abstract

Glycoproteins binding to Ulex europaeus agglutinin-I (UEA-I) lectin, which recognizes the terminal alpha-L-fucose residue, were analyzed in 18 cases of human colorectal carcinoma by sodium dodecyl sulfate-polyacrylamide gel electrophoresis followed by the Western blotting method. In the distal large bowel (descending and sigmoid colon and rectum), high-molecular-weight glycoproteins binding to UEA-I existed in carcinoma tissue but not in normal mucosa. In the proximal large bowel (ascending and transverse colon), high-molecular-weight glycoproteins binding to UEA-I were found both in normal mucosa and in carcinoma tissue, whereas those from the carcinoma tissue had an apparently lower molecular weight as compared to the weight of those from the normal mucosa. Thus there is a biochemical difference in UEA-I binding glycoproteins between the normal mucosa and the carcinoma tissue, although in our previous histochemical study no difference was observed in UEA-I binding glycoproteins of the proximal large bowel between the carcinoma tissue and the normal mucosa. Furthermore, carcinoembryonic antigen from the carcinoma tissue was found to have the same electrophoretical mobility as the UEA-I binding glycoproteins.

摘要

通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳及蛋白质印迹法,对18例人类结直肠癌中与荆豆凝集素-I(UEA-I)结合的糖蛋白进行了分析,UEA-I可识别末端α-L-岩藻糖残基。在远端大肠(降结肠、乙状结肠和直肠),癌组织中存在与UEA-I结合的高分子量糖蛋白,而正常黏膜中不存在。在近端大肠(升结肠和横结肠),正常黏膜和癌组织中均发现了与UEA-I结合的高分子量糖蛋白,然而癌组织中的糖蛋白分子量明显低于正常黏膜中的糖蛋白分子量。因此,正常黏膜和癌组织中与UEA-I结合的糖蛋白存在生化差异,尽管在我们之前的组织化学研究中,近端大肠的癌组织和正常黏膜中UEA-I结合糖蛋白未观察到差异。此外,发现癌组织中的癌胚抗原与UEA-I结合糖蛋白具有相同的电泳迁移率。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验