肿瘤相关碳水化合物结构与人类乳腺癌基因扩增相关的预后价值

T Fukutomi, S Hirohashi, H Tsuda, T Nanasawa, H Yamamoto, M Itabashi, Y Shimosato
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引用次数: 6

摘要

研究了细胞表面糖链结合乳腺癌某些基因扩增对患者预后的影响,并评价了癌细胞糖链与原癌基因c-myc、int-2和c- erbb -2扩增之间的关系。采用免疫组化技术,用1凝集素(HPA)结合亲和生物素-过氧化物酶法对153例人乳腺癌组织进行了研究;Helix Pomatia)和4个单克隆抗体(B-72-3, St-439, anti-Tn和anti-T)。HPA、St-439、B-72-3、anti-Tn和anti-T的阳性率分别为43%(63/153)、52%(80/153)、53%(81/153)、64%(98/153)和89%(136/153)。HPA染色阳性患者的生存率低于HPA染色阴性患者(p < 0.05), St-439染色阳性患者的预后优于St-439染色阴性患者(p < 0.01)。HPA阳性率与c-myc原癌基因扩增相关(p < 0.01), St-439阳性率与c- erbb -2基因扩增相关(p < 0.01)。这些数据表明HPA和St-439的预后价值,以及基因扩增与乳腺癌细胞碳水化合物结构之间的关系。
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The prognostic value of tumor-associated carbohydrate structures correlated with gene amplifications in human breast carcinomas.

The effects of cell surface sugar chains combined with certain gene amplifications of breast cancers on the prognosis of patients were studied and the relationships between the sugar chains of cancer cells and amplifications of the proto-oncogenes c-myc, int-2 and c-erb B-2, evaluated. One hundred and fifty three human breast carcinoma tissues were investigated by an immunohistochemical technique using the avidinbiotin-peroxidase method with 1 lectin (HPA; Helix Pomatia) and 4 monoclonal antibodies (B-72-3, St-439, anti-Tn and anti-T). The positive rates of HPA, St-439, B-72-3, anti-Tn and anti-T were 43 per cent (63/153), 52 per cent (80/153), 53 per cent (81/153), 64 per cent (98/153) and 89 per cent (136/153), respectively. Patients whose cancers had positive HPA staining were found to have a lower survival rate than those with negative HPA staining (p less than 0.05), whereas those whose cancers had positive St-439 staining showed a better prognosis than those with negative St-439 staining (p less than 0.01). The positive rate of HPA was related to the gene amplification of c-myc proto-oncogene (p less than 0.01), whereas the negative rate of St-439 was correlated with the gene amplification of c-erb B-2 (p less than 0.01). These data indicate the prognostic value of HPA and St-439 and also the relationships between the gene amplifications and carbohydrate structures in breast cancer cells.

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