Toshkov I A, Chaney W G, Colcher D M, Hollingsworth M A, Bratanova T K, Perini F, Pour P M
Eppley Cancer Center, University of Nebraska Medical Center, Omaha 68198-6805, USA.
Int J Pancreatol. 1995 Dec;18(3):249-55. doi: 10.1007/BF02784949.
An adhesion factor, produced by the hamster pancreatic cancer cell line PC-1.0, was tested for its efficiency in promoting the in vitro adhesion of normal and tumor cells (pancreas, lung, kidney, colon, breast, skin, prostate, neuroblast, melanocyte) derived from human, monkey, bovine, hamster, and rat sources. Using a modification of the dimethylthyazol diphenyl tetrazolium (MTT) assay, the factor was found to induce adhesion in all cell lines in a dose-dependent manner. Although the effect was variously expressed, there was a statistically significant difference between the MTT absorbance of cells incubated in the presence or absence of the factor. Conditioned medium of each cell line tested showed significantly less adhesion effect than that produced by PC-1.0 cells. Because our previous study indicated that the adhesion factor produced by PC-1.0 cells differed from known growth factors and adhesion molecules including fibronectin, vibronectin, laminin, and collagen, it appears that PC-1.0 cells produce a novel adhesion factor that enhances adherence of normal and malignant cells of different species.
对仓鼠胰腺癌细胞系PC-1.0产生的一种黏附因子进行了测试,以检验其促进源自人、猴、牛、仓鼠和大鼠的正常细胞及肿瘤细胞(胰腺、肺、肾、结肠、乳腺、皮肤、前列腺、神经母细胞、黑素细胞)体外黏附的效率。采用改良的二甲基噻唑二苯基四氮唑(MTT)分析法,发现该因子能以剂量依赖方式诱导所有细胞系发生黏附。尽管效应表现各异,但在有或无该因子存在的情况下孵育的细胞,其MTT吸光度之间存在统计学上的显著差异。所测试的每个细胞系的条件培养基显示出的黏附效应明显低于PC-1.0细胞产生的黏附效应。由于我们之前的研究表明,PC-1.0细胞产生的黏附因子不同于已知的生长因子和黏附分子,包括纤连蛋白、玻连蛋白、层粘连蛋白和胶原蛋白,所以PC-1.0细胞似乎产生了一种新型黏附因子,可增强不同物种正常细胞和恶性细胞的黏附。