Suppr超能文献

正常及癌前口腔黏膜上皮和鳞状细胞癌中凝集素结合的差异

Differential lectin-bindings in normal and precancerous epithelium and squamous cell carcinoma of the oral mucosa.

作者信息

Saku T, Okabe H

机构信息

Department of Pathology, Nagasaki University School of Dentistry, Japan.

出版信息

J Oral Pathol Med. 1989 Sep;18(8):438-45. doi: 10.1111/j.1600-0714.1989.tb01340.x.

Abstract

In order to establish a useful and objective marker of malignancy of oral mucosa, the binding sites for Ulex europaeus agglutinin I (UEA-I). Bandeiraea simplicifolia agglutinin I (BSA-I) and peanut agglutinin (PNA) were comparatively examined in the surgical materials from the normal, dysplastic and cancerous epithelium of the oral mucosa by a novel lectin-antilectin immunoperoxidase method. Based on the staining patterns of the normal keratinized epithelium, UEA-I was regarded as the marker for the prickle cells, BSA-I for the cells in the upper prickle to the horny layers, and PNA for those in the basal layer. As the degree of dysplasia advanced, all layers of epithelium came to react with UEA-I and PNA, whereas the BSA-I binding was negative. Positive reactions for UEA-I and PNA were seen in most carcinoma cells other than the keratinizing foci stained by BSA-I. The results indicate that a UEA-I-positive reaction in the basal cells, a PNA-positive in the prickle cells and loss of receptor for BSA-I occur in the course of malignant transformation of oral mucosa, and that these lectins may be regarded as useful markers of oral epithelial cytoplasmic differentiation.

摘要

为了建立一种有用且客观的口腔黏膜恶性肿瘤标志物,采用一种新型凝集素 - 抗凝集素免疫过氧化物酶方法,对口腔黏膜正常、发育异常及癌性上皮的手术材料中欧洲荆豆凝集素I(UEA - I)、单叶豆凝集素I(BSA - I)和花生凝集素(PNA)的结合位点进行了比较研究。根据正常角化上皮的染色模式,UEA - I被视为棘细胞的标志物,BSA - I为上棘层至角质层细胞的标志物,PNA为基底层细胞的标志物。随着发育异常程度的加重,上皮各层均开始与UEA - I和PNA发生反应,而BSA - I结合呈阴性。除了被BSA - I染色的角化灶外,大多数癌细胞中可见UEA - I和PNA的阳性反应。结果表明,口腔黏膜恶性转化过程中,基底细胞出现UEA - I阳性反应、棘细胞出现PNA阳性反应以及BSA - I受体丧失,并且这些凝集素可被视为口腔上皮细胞质分化的有用标志物。

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