Zucker S, Beck G, DiStefano J F, Lysik R M
Br J Cancer. 1985 Aug;52(2):223-32. doi: 10.1038/bjc.1985.181.
The crucial role of non-plasminogen dependent serine proteinases is tissue invasive and cytolytic functions of Walker 256 cancer cells has been documented using a rat urinary bladder invasion and a 125I-labelled fibroblast cytolysis assay. The invasive capacity of these cancer cells was abrogated by non toxic concentrations of the serine proteinase inhibitors, diisopropylfluorophosphate and phenylmethylsulfonylfluoride, but not by metallo or cysteine proteinase inhibitors. Although tumour cell collagenase activity and plasminogen activator were demonstrated, these proteolytic enzymes were not essential in these in vitro assays. These results suggest that different categories of proteinases play specific roles in the complicated process of cancer invasion.
非纤溶酶原依赖性丝氨酸蛋白酶在沃克256癌细胞的组织侵袭和细胞溶解功能中起关键作用,这已通过大鼠膀胱侵袭实验和125I标记的成纤维细胞溶解实验得到证实。这些癌细胞的侵袭能力可被无毒浓度的丝氨酸蛋白酶抑制剂二异丙基氟磷酸酯和苯甲基磺酰氟消除,但金属蛋白酶或半胱氨酸蛋白酶抑制剂则不能。尽管已证明肿瘤细胞具有胶原酶活性和纤溶酶原激活剂,但在这些体外实验中,这些蛋白水解酶并非必需。这些结果表明,不同类别的蛋白酶在癌症侵袭的复杂过程中发挥着特定作用。