与侵殖相关的蛋白酶及其在细胞外基质降解中的作用。

Enzyme & protein Pub Date : 1996-01-01 DOI:10.1159/000468616
W T Chen
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引用次数: 131

摘要

转移性癌细胞通过质膜突侵入细胞外基质,接触并溶解基质。有证据表明,170-kD明胶酶(seprase)和明胶酶A等膜相关蛋白酶在侵殖虫中发挥其作用机制。本文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、meprin、二肽基肽酶IV、成纤维细胞活化蛋白α和胍基苯甲酸酶在细胞表面蛋白水解中的潜在作用。有人提出,在侵殖上形成的结构和功能连接的蛋白酶复合物允许癌细胞侵入细胞外基质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Proteases associated with invadopodia, and their role in degradation of extracellular matrix.

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.

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