Konska G, Favy D, Guillot J, Bernard-Gallon D, de Latour M, Fonck Y
Départment de Biologie Cellulaire, Faculté de Pharmacie, Université de Clermont I, Clermont-Ferrand.
C R Seances Soc Biol Fil. 1998;192(4):733-47.
Expression of carcinoembryonic Tn antigen studied with VVA-B4 and GSI-A4 lectins with the monoclonal antibody 83D4 and of T antigen with LDL and PNA lectins with the monoclonal antibody ZCMO4, were examined in 54 malignant or benign human breast tumors and for MCF-7, T47D and MCF-10A cell lines of human breast tumors origin. For breast tissues, positive membrane labelling with D-GalNAc alpha-O-ser/thr (Tn-antigen) specific lectins and 83D4 MAb occurred in benign cases indicating that modification of glycoconjugates may precede the cytologic anomalies. In fibroadenoma, fibrocystic dystrophy, ductal hyperplasia and grade I invasive ductal carcinomas, the binding sites for lectins and 83D4 MAb were essentially on the cell membrane with labelling of both apical and basolateral compartments. In grade II and III, the labelling involved the cytoplasma, and cell heterogeneity appeared. The disappearance of reactivity observed for a large proportion of cells at grade III may be due either to the loss of glycosyltransferase, or to the lack of synthesis of the protein back-bone. Invasive lobular carcinomas showed labelling both on apical membrane and the outermost part of the cytoplasm with a distinct cell polarity. Lectin receptors are present at the surface of metastatic cells, possibly related to their involvement in adhesion. In all cases, T or sialosyl-T antigens are present at the surface of tumors cells. All cell lines from breast tumors cultured in vitro were labelled with lectins and monoclonal antibodies. The simultaneous presence of Tn and T antigens on the cells, indicates that the expression of Tn antigen is due to a partial but non total deficiency in the beta-1- > 3 galactosyltransferase involved in T-antigen synthesis.
用VVA - B4和GSI - A4凝集素以及单克隆抗体83D4研究癌胚性Tn抗原的表达,并用LDL和PNA凝集素以及单克隆抗体ZCMO4研究T抗原的表达,对54例人乳腺良恶性肿瘤以及源自人乳腺肿瘤的MCF - 7、T47D和MCF - 10A细胞系进行了检测。对于乳腺组织,在良性病例中出现了用D - GalNAcα - O - ser/thr(Tn抗原)特异性凝集素和83D4单克隆抗体进行的阳性膜标记,这表明糖缀合物的修饰可能先于细胞异常。在纤维腺瘤、纤维囊性营养不良、导管增生和I级浸润性导管癌中,凝集素和83D4单克隆抗体的结合位点主要在细胞膜上,顶端和基底外侧区均有标记。在II级和III级肿瘤中,标记涉及细胞质,且出现了细胞异质性。在III级时观察到大部分细胞反应性消失,这可能是由于糖基转移酶的丧失,或者是蛋白质骨架合成的缺乏。浸润性小叶癌在顶端膜和细胞质最外层均有标记,具有明显的细胞极性。凝集素受体存在于转移细胞表面,可能与其参与黏附有关。在所有病例中,T或唾液酸 - T抗原存在于肿瘤细胞表面。所有体外培养的乳腺肿瘤细胞系均用凝集素和单克隆抗体进行了标记。细胞上同时存在Tn和T抗原,表明Tn抗原的表达是由于参与T抗原合成的β1→3半乳糖基转移酶部分但非完全缺乏所致。