Brennan M J, Oldberg A, Hayman E G, Ruoslahti E
Cancer Res. 1983 Sep;43(9):4302-7.
In this paper, we demonstrate that a chondroitin sulfate proteoglycan purified from a rat yolk sac tumor alters the adhesion of the tumor cells to substrata containing fibronectin or type I collagen. In the presence of the proteoglycan, these substrata were much less adhesive and did not promote cell spreading. The inhibitory effect of the proteoglycan was reversible and more pronounced during the early stages of cell attachment in vitro. The effect of the proteoglycan was selective in that it depended on the ability of the adhesive substratum to bind the proteoglycan. The proteoglycan did not inhibit the attachment of the cells to type IV collagen, which bound 12 times less proteoglycan than did type I collagen. Similarly, attachment of the cells to fibronectin fragments which did not bind the proteoglycan was not affected by it. The selective effects of the proteoglycan on the adhesion of cells to extracellular matrices suggest that such proteoglycans may promote tumor invasion by reducing interaction of cells with interstitial extracellular matrices while permitting attachment to basement membranes.
在本文中,我们证明从大鼠卵黄囊肿瘤中纯化得到的一种硫酸软骨素蛋白聚糖可改变肿瘤细胞与含有纤连蛋白或I型胶原的基质的黏附。在该蛋白聚糖存在的情况下,这些基质的黏附性大大降低,且不促进细胞铺展。该蛋白聚糖的抑制作用是可逆的,且在体外细胞黏附的早期阶段更为明显。该蛋白聚糖的作用具有选择性,因为它取决于黏附基质结合该蛋白聚糖的能力。该蛋白聚糖不抑制细胞与IV型胶原的黏附,IV型胶原结合的蛋白聚糖比I型胶原少12倍。同样,细胞与不结合该蛋白聚糖的纤连蛋白片段的黏附不受其影响。该蛋白聚糖对细胞与细胞外基质黏附的选择性作用表明,此类蛋白聚糖可能通过减少细胞与间质细胞外基质的相互作用同时允许细胞黏附于基底膜来促进肿瘤侵袭。