Limas C, Lange P
Cancer. 1986 Sep 15;58(6):1236-45. doi: 10.1002/1097-0142(19860915)58:6<1236::aid-cncr2820580611>3.0.co;2-i.
The expression of the Thomsen-Friedenreich antigen (T-antigen) in normal and neoplastic urothelium was investigated using paraffin-processed and fresh frozen tissue sections obtained by biopsy from 56 patients. The T-antigen was detected through its binding to the peanut agglutinin (PNA) with two methods: a biotin-avidin-peroxidase system or a modified red cell adherence test. In vitro treatment of the tissue sections with neuraminidase induced PNA binding in the normal and neoplastic urothelium as well as the red blood cells and the vascular endothelium. Spontaneous PNA binding was absent in normal bladder epithelium, but was observed in 10% of the noninvasive and 65% of the invasive transitional cell carcinomas (TCC). The positive reactions were seen in the cytoplasm, cell surface, and mucin. These results were correlated with the light and electron microscopic findings and with the detectability of the A, B, H blood group antigens in the same tissues. Ultrastructurally, the PNA binding sites frequently corresponded to the Golgi apparatus and to secretory products which stained with Alcian blue. About 90% of TCCs with spontaneous PNA binding did not express the expected blood group antigen. The latter was also undetectable in 54% of TCCs lacking spontaneous PNA binding. It appears, therefore, that the expression of T-antigen occurs later in the evolution of aggressive TCCs, usually when they have advanced to invasive stages. The finding of spontaneous T-antigen unmasking correlates with the presence of invasion and a higher risk for metastatic involvement of regional lymph nodes.
利用从56例患者活检获取的石蜡处理和新鲜冷冻组织切片,研究了正常和肿瘤性尿路上皮中汤姆森 - 弗里德赖希抗原(T抗原)的表达。通过两种方法检测T抗原与花生凝集素(PNA)的结合:生物素 - 抗生物素蛋白 - 过氧化物酶系统或改良的红细胞粘附试验。用神经氨酸酶对组织切片进行体外处理,可诱导正常和肿瘤性尿路上皮以及红细胞和血管内皮细胞与PNA结合。正常膀胱上皮中不存在自发的PNA结合,但在10%的非侵袭性和65%的侵袭性移行细胞癌(TCC)中观察到。阳性反应见于细胞质、细胞表面和粘蛋白。这些结果与光镜和电镜检查结果以及同一组织中A、B、H血型抗原的可检测性相关。在超微结构上,PNA结合位点常与高尔基体和用阿尔辛蓝染色的分泌产物相对应。约90%具有自发PNA结合的TCC未表达预期的血型抗原。在54%缺乏自发PNA结合的TCC中也检测不到后者。因此,似乎T抗原的表达在侵袭性TCC的进展过程中出现得较晚,通常是在它们发展到侵袭阶段时。自发T抗原暴露的发现与侵袭的存在以及区域淋巴结转移受累的较高风险相关。