Orntoft T F, Nielsen M J, Wolf H, Olsen S, Clausen H, Hakomori S, Dabelsteen E
Department of Surgery I, Aarhus County Hospital, Denmark.
Cancer. 1987 Dec 1;60(11):2641-8. doi: 10.1002/1097-0142(19871201)60:11<2641::aid-cncr2820601112>3.0.co;2-5.
The deletion of blood group ABO antigen expression in bladder carcinoma has attracted attention because of its potential as a prognostic parameter. Based on recently produced monoclonal antibodies against blood group antigens, it has become possible to elucidate the carcinoma-associated modulation of these antigens at a molecular level. In this study we have used a panel of monoclonal antibodies (H, Lea, Leb, A, ALeb) that are specific to type 1 chain structures. By the use of an immunohistochemical method, the histologic and cytologic location of these antigens in the urothelium was studied in 25 biopsies from transitional cell carcinomas and compared to 21 previously examined normal biopsies. Urothelial blood group reactivity was compared to Lewis and secretor status. The authors found a series of events associated with neoplastic progression of noninvasive urothelium: a disruption of the orderly stratification of blood group antigens in different cell layers; cytostructural relocation of cytoplasmic antigens to the cell surface; loss of correlation between urothelial blood group antigens and secretor status; and gradual deletion of antigens. In the invasive tissue these events were followed by a total deletion of A and H isoantigens and uniform expression of Lewis b and sialyted Lewis a antigen. These findings indicate that there is a complex modulation of blood group antigen biosynthesis associated with the neoplastic progression of the human urothelium.
膀胱癌中血型ABO抗原表达的缺失因其作为预后参数的潜力而受到关注。基于最近产生的针对血型抗原的单克隆抗体,已能够在分子水平阐明这些抗原与癌症相关的调节情况。在本研究中,我们使用了一组对1型链结构具有特异性的单克隆抗体(H、Lea、Leb、A、ALeb)。通过免疫组织化学方法,在25例移行细胞癌活检组织中研究了这些抗原在尿路上皮中的组织学和细胞学定位,并与21例先前检查的正常活检组织进行了比较。将尿路上皮血型反应性与Lewis和分泌状态进行了比较。作者发现了一系列与非侵袭性尿路上皮肿瘤进展相关的事件:不同细胞层中血型抗原有序分层的破坏;细胞质抗原向细胞表面的细胞结构重新定位;尿路上皮血型抗原与分泌状态之间相关性的丧失;以及抗原的逐渐缺失。在侵袭性组织中,这些事件之后是A和H同种抗原的完全缺失以及Lewis b和唾液酸化Lewis a抗原的均匀表达。这些发现表明,与人类尿路上皮肿瘤进展相关的血型抗原生物合成存在复杂的调节。