Suzuki K, Ono T, Umeda M, Itoh H
Department of Biochemistry, Kanagawa Cancer Center Research Institute, Japan.
Int J Cancer. 1992 Nov 11;52(5):818-26. doi: 10.1002/ijc.2910520525.
Production of cell-adhesion proteins was examined in 10 cell lines and 5 cultured human cancer cells at an early passage. Two-thirds of the tested cells produced and secreted into their culture medium variable amounts of material active in promoting cell attachment. One of the rectal carcinoma cell lines, CaR-I, grew well in serum-free medium and secreted a large amount of the active principle. The active principles produced by CaR-I cells were characterized after partial purification, and were found to be fibronectin and its fragments. The presence of fibronectin and its fragments was proved by the following facts: (1) reactivity to the monoclonal antibodies which recognize different epitopes of fibronectin, and (2) reactivity to RGD peptide which is the attachment sequence of fibronectin. In addition to fibronectin and its fragments, CaR-I cells were also shown to produce a 53-kDa attachment factor. Unexpectedly, the protein was proved to be most probably the p53 suppressor gene product.
在10种细胞系和5种早期传代的培养人癌细胞中检测了细胞粘附蛋白的产生情况。三分之二的受试细胞产生并分泌到其培养基中的具有促进细胞附着活性的物质数量不等。其中一种直肠癌细胞系CaR-I在无血清培养基中生长良好,并分泌大量活性成分。CaR-I细胞产生的活性成分经部分纯化后进行了表征,发现是纤连蛋白及其片段。纤连蛋白及其片段的存在可通过以下事实得到证明:(1)与识别纤连蛋白不同表位的单克隆抗体发生反应,以及(2)与作为纤连蛋白附着序列的RGD肽发生反应。除了纤连蛋白及其片段外,CaR-I细胞还被证明能产生一种53 kDa的附着因子。出乎意料的是,该蛋白很可能被证明是p53抑癌基因产物。