Terranova V P, Hujanen E S, Loeb D M, Martin G R, Thornburg L, Glushko V
Proc Natl Acad Sci U S A. 1986 Jan;83(2):465-9. doi: 10.1073/pnas.83.2.465.
Malignant cells must traverse basement membranes during their migration to sites distant from the primary tumor. Since basement membranes are thought to be a critical barrier to the passage of tumor cells, we have constructed a model basement membrane-stromal matrix consisting of laminin and type IV collagen reconstituted onto a disk of type I collagen for use in an in vitro assay of invasiveness. Metastatic tumor cells and leukocytes are able to cross this barrier, whereas nonmetastatic tumor cells, fibroblasts, and epidermal cells cannot penetrate it. Those tumor cells that penetrate the barriers were found, when isolated and subcultured, to be more invasive and to produce more metastases than the parental population. This assay system should be useful for studying the invasiveness of tumor cells and for isolating highly invasive variants.
恶性细胞在迁移至远离原发肿瘤的部位时必须穿过基底膜。由于基底膜被认为是肿瘤细胞通过的关键屏障,我们构建了一种模型基底膜 - 基质,其由层粘连蛋白和IV型胶原蛋白重构到I型胶原蛋白圆盘上,用于体外侵袭性测定。转移性肿瘤细胞和白细胞能够穿过这一屏障,而非转移性肿瘤细胞、成纤维细胞和表皮细胞则无法穿透。那些穿透屏障的肿瘤细胞在分离和传代培养后,被发现比亲代群体更具侵袭性且能产生更多转移灶。该测定系统对于研究肿瘤细胞的侵袭性以及分离高侵袭性变体应是有用的。