基质金属蛋白酶
蛋白酵素
血管生成
细胞生物学
蛋白质水解
转移
运动性
金属蛋白酶
生物
基质金属蛋白酶抑制剂
细胞外基质
化学
癌症研究
生物化学
癌症
酶
遗传学
作者
Sonia Hernandez‐Barrantes,M. Margarida Bernardo,Márta Tóth,Rafael Fridman
标识
DOI:10.1006/scbi.2001.0421
摘要
Pericellular proteolysis is a hallmark of tumor cell metastasis. The membrane type (MT)-matrix metalloproteinases (MMPs) constitute a distinctive group of membrane-bound MMPs that are central mediators of surface proteolytic events that regulate tumor cell motility, metastasis and angiogenesis. As membrane-tethered proteases, the MT-MMPs exhibit unique regulatory mechanisms and interactions with metalloproteinase inhibitors and other relevant molecules. This review will focus on new emerging information on the mechanisms that regulate MT-MMP processing, activity and inhibition , and their significance for enzyme function in the tumor microenvironment.
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