Ohshio G, Yoshioka H, Manabe T, Sakahara H, Yamabe H, Imamura M, Inoue M, Tanaka N, Nakada H, Yamashina I
Department of Surgery, Faculty of Medicine, Kyoto University, Japan.
J Cancer Res Clin Oncol. 1994;120(6):325-30. doi: 10.1007/BF01247457.
Oncogenic transformation is often associated with changes in the glycosylation state of malignant cells. We investigated the immunohistochemical localization of sialosyl-Tn antigen [O-linked NeuAc(alpha 2-->6)GAINAc] using a novel monoclonal antibody MLS102 in normal and malignant digestive-tract tissues. In normal tissues, weak MLS102 immunoreactivity was observed in the epithelium of the esophagus, stomach and colon. However, MLS102 immunoreactivity was strong in the goblet cells of the duodenum, but not in the Brunner glands. In carcinomas of the esophagus, stomach, colon, pancreas and biliary tract, positive staining was detected with a high frequency (80%-100%). In mucinous carcinomas and signet-ring cell carcinomas, malignant cells themselves and the mucins they secreted were strongly positive for sialosyl-Tn antigen. There was no significant correlation between the frequency of expression of sialosyl-Tn antigen and the degree of differentiation (grade). However, in the case of well-differentiated adenocarcinomas, sialosyl-Tn antigen was found mainly in the supranuclear areas (Golgi area), on the apical surface and in the adjacent cytoplasm. In poorly differentiated adenocarcinomas, the antigen was often detected in the whole plasma membrane and cytoplasm. Therefore, monoclonal antibody MLS102 may be useful in further elucidating the characteristics of digestive-tract cancers, and possibly in their treatment.
致癌转化通常与恶性细胞糖基化状态的改变有关。我们使用新型单克隆抗体MLS102研究了唾液酸-Tn抗原[O-连接的NeuAc(α2→6)GalNAc]在正常和恶性消化道组织中的免疫组织化学定位。在正常组织中,食管、胃和结肠的上皮中观察到弱的MLS102免疫反应性。然而,MLS102免疫反应性在十二指肠的杯状细胞中较强,但在十二指肠腺中则没有。在食管癌、胃癌、结肠癌、胰腺癌和胆管癌中,高频检测到阳性染色(80%-100%)。在黏液癌和印戒细胞癌中,恶性细胞本身及其分泌的黏蛋白对唾液酸-Tn抗原呈强阳性。唾液酸-Tn抗原的表达频率与分化程度(分级)之间没有显著相关性。然而,在高分化腺癌中,唾液酸-Tn抗原主要存在于核上区(高尔基体区)、顶端表面和相邻的细胞质中。在低分化腺癌中,该抗原常出现在整个质膜和细胞质中。因此,单克隆抗体MLS102可能有助于进一步阐明消化道癌症的特征,并可能用于其治疗。