Stallmach A, Riese H H, Schuppan D, Bornhöft G, Stein H, Riecken E O
Freie Universität Berlin, Klinikum Steglitz, FRG.
Gut. 1991 Mar;32(3):282-6. doi: 10.1136/gut.32.3.282.
The adhesive properties of tumour cells to laminin, the major glycoprotein of basement membranes, play a crucial part in the complex process of tumour invasion and metastasis. We therefore investigated the expression of laminin binding proteins in isolated basolateral cell membranes of human colorectal carcinomas and the adjacent normal colonic mucosa. Cell membrane binding assays and immunoblotting experiments showed appreciable quantitative and qualitative differences in the expression of these proteins in neoplastic and normal tissue. Epithelial basolateral cell membranes of colorectal carcinomas bound five to eight times more radioactive labelled laminin than basolateral cell membranes of the adjacent normal colonic epithelium. The expression of laminin binding proteins with Mr 66,000-69,000 daltons corresponding to the so called 'Mr 67,000 dalton laminin receptor' was three to four times higher in colorectal carcinomas than in normal colonic epithelium. In addition, laminin binding proteins with higher molecular weights, which may be related to the family of integrins, were also increased in colorectal carcinomas. In particular, laminin binding proteins with Mr 180,000 daltons were exclusively expressed on neoplastic epithelial cells of human colorectal carcinomas. Our data suggest that certain classes of laminin binding proteins may be selectively expressed on colonic tumour cells, leading to an increased capacity for migration, invasion, and metastasis.
肿瘤细胞与基底膜的主要糖蛋白层粘连蛋白的黏附特性,在肿瘤侵袭和转移的复杂过程中起着关键作用。因此,我们研究了人结肠直肠癌及相邻正常结肠黏膜分离的基底外侧细胞膜中层粘连蛋白结合蛋白的表达情况。细胞膜结合试验和免疫印迹实验表明,这些蛋白在肿瘤组织和正常组织中的表达在数量和质量上存在明显差异。结肠直肠癌的上皮基底外侧细胞膜结合的放射性标记层粘连蛋白比相邻正常结肠上皮的基底外侧细胞膜多五到八倍。分子量为66,000 - 69,000道尔顿的层粘连蛋白结合蛋白(对应所谓的“67,000道尔顿层粘连蛋白受体”)在结肠直肠癌中的表达比正常结肠上皮高3 - 4倍。此外,分子量较高的层粘连蛋白结合蛋白(可能与整合素家族有关)在结肠直肠癌中也有所增加。特别是,分子量为180,000道尔顿的层粘连蛋白结合蛋白仅在人结肠直肠癌的肿瘤上皮细胞上表达。我们的数据表明,某些类别的层粘连蛋白结合蛋白可能在结肠肿瘤细胞上选择性表达,从而导致迁移、侵袭和转移能力增强。