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正常及恶性膀胱尿路上皮中ABH血型相关抗原:浸润性癌中2型链ABH抗原缺失的可能结构基础。

Blood group ABH-related antigens in normal and malignant bladder urothelium: possible structural basis for the deletion of type-2 chain ABH antigens in invasive carcinomas.

作者信息

Orntoft T F, Wolf H, Clausen H, Dabelsteen E, Hakomori S

机构信息

Danish Cancer Society, Department of Experimental Clinical Oncology, Aarhus.

出版信息

Int J Cancer. 1989 May 15;43(5):774-80. doi: 10.1002/ijc.2910430505.

Abstract

A complete panel of mouse monoclonal antibodies (MAbs) against Type-2 chain (GaI beta I-4GlcNAc-R) blood-group antigens (N-acetyl-lactosamine, Lex, H, Ley, A monofucosylated, Aley, repetitive A) was used in a detailed immunohistological study of the modulation of these carbohydrate antigens in transitional-cell carcinomas. The histological and cellular locations of these antigens were studied in 19 normal bladder biopsies and 53 transitional-cell carcinomas with as well as without neuraminidase treatment of tissue sections in order to uncover potential sialylated antigens. The antigen expression was correlated to individual A1A2BO, Lewis, and secretor status. Several alterations of blood group expression were found: (1) loss of A and H antigens with accumulation of Ley antigens; (2) loss of correlation between antigen expression and secretor status; (3) disruption of the orderly stratification of blood-group antigen expression in relation to cell layers; and (4) changes in subcellular location of antigen expression. The present data indicate that deletion of Type-2 chain ABH antigens in transitional-cell carcinomas is associated with alpha 1-3 fucosylation of the H antigen leading to accumulation of Ley antigens.

摘要

一组完整的针对2型链(GaIβI-4GlcNAc-R)血型抗原(N-乙酰乳糖胺、Lex、H、Ley、单岩藻糖基化的A、Aley、重复A)的小鼠单克隆抗体(MAbs)被用于对移行细胞癌中这些碳水化合物抗原调节的详细免疫组织学研究。在19例正常膀胱活检组织和53例移行细胞癌中,研究了这些抗原的组织学和细胞定位,同时对组织切片进行了神经氨酸酶处理或未处理,以发现潜在的唾液酸化抗原。抗原表达与个体的A1A2BO、Lewis和分泌状态相关。发现了血型表达的几种改变:(1)A和H抗原丢失,Ley抗原积累;(2)抗原表达与分泌状态之间的相关性丧失;(3)血型抗原表达与细胞层相关的有序分层破坏;(4)抗原表达的亚细胞定位改变。目前的数据表明,移行细胞癌中2型链ABH抗原的缺失与H抗原的α1-3岩藻糖基化有关,导致Ley抗原积累。

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