Reich R, Thompson E W, Iwamoto Y, Martin G R, Deason J R, Fuller G C, Miskin R
Laboratory of Developmental Biology and Anomalies, National Institute of Dental Research, Bethesda, Maryland 20892.
Cancer Res. 1988 Jun 15;48(12):3307-12.
Using both human and murine cell lines, we show that malignant cells are able to invade through basement membrane and also secrete elevated amounts of collagenase IV, an enzyme implicated in the degradation of basement membranes. Using serine proteinase inhibitors and antibodies to plasminogen activators as well as a newly described collagenase inhibitor we demonstrate that a protease cascade leads to the activation of an enzyme(s) that cleaves collagen IV. Inhibition at each step reduces the invasion of the tumor cells through reconstituted basement membrane in vitro. Treatment with a collagenase inhibitor reduced the incidence of lung lesions in mice given i.v. injections of malignant melanoma cells.
利用人类和小鼠细胞系,我们发现恶性细胞能够穿透基底膜,并且还会分泌大量的IV型胶原酶,这种酶与基底膜的降解有关。使用丝氨酸蛋白酶抑制剂、针对纤溶酶原激活剂的抗体以及一种新描述的胶原酶抑制剂,我们证明了蛋白酶级联反应会导致一种能够切割IV型胶原的酶被激活。在体外,对每一步的抑制都会减少肿瘤细胞穿透重组基底膜的侵袭能力。用胶原酶抑制剂处理可降低静脉注射恶性黑色素瘤细胞的小鼠肺部病变的发生率。