Chen W T
Department of Cell Biology, Georgetown University School of Medicine, Washington, D.C. 20007, USA.
Enzyme Protein. 1996;49(1-3):59-71. doi: 10.1159/000468616.
Metastasizing cancer cells invade the extracellular matrix using plasma membrane protrusions (invadopodia) that contact and dissolve the matrix. Evidence suggests that membrane-associated proteases, 170-kD gelatinase (seprase) and Gelatinase A, exert their mechanisms of action on invadopodia. Potential roles that other metallo- and serine-types of membrane proteases, including membrane-type matrix metalloprotease, meprin, dipeptidyl peptidase IV, fibroblast activation protein alpha and guanidinobenzoatase, play in the cell surface proteolysis are also discussed. It is proposed that formation of a structurally and functionally linked protease complex on invadopodia allows the invasion of cancer cells into the extracellular matrix.
转移性癌细胞利用与质膜接触并溶解细胞外基质的突起(侵袭伪足)侵入细胞外基质。有证据表明,膜相关蛋白酶,即170-kD明胶酶(分离酶)和明胶酶A,在侵袭伪足上发挥其作用机制。还讨论了其他金属和丝氨酸类型的膜蛋白酶,包括膜型基质金属蛋白酶、膜联蛋白、二肽基肽酶IV、成纤维细胞激活蛋白α和胍基苯甲酰酶在细胞表面蛋白水解中所起的潜在作用。有人提出,侵袭伪足上形成结构和功能相连的蛋白酶复合物可使癌细胞侵入细胞外基质。