毛皮
生物
头颈部鳞状细胞癌
免疫印迹
细胞培养
蛋白酵素
癌症研究
表皮样癌
基质金属蛋白酶
细胞
分子生物学
癌症
酶
头颈部癌
基因
生物化学
遗传学
作者
Daniel E. Bassi,Haleh Mahloogi,Luma F. Al-Saleem,Ricardo López de Cicco,John A. Ridge,Andres J. Klein–Szanto
摘要
Abstract Pro‐protein convertases (PCs) are proteases that recognize and cleave precursor proteins. Furin, a well‐studied PC, is ubiquitously expressed, and it has been implicated in many physiological and pathological processes. Some substrates for furin, such as membrane type 1 (MT1) matrix metalloproteinase (MMP), an MMP that activates gelatinase, a collagen‐degrading enzyme, are associated with the advanced malignant phenotype. This report examines the expression of furin in carcinoma cell lines of different invasive ability. The levels of furin mRNA and protein correlated with the aggressiveness of tumor cell lines derived from head and neck and lung cancers. Furin expression also was investigated in primary head and neck squamous cell carcinomas (HNSCCs). Furin mRNA was not detected in nonmetastasizing carcinomas. In contrast, furin mRNA was expressed in metastasizing HNSCCs. Immunohistochemistry and Western blot analysis confirmed these results at the protein level. Furin activity was investigated indirectly by evaluating the expression of the pro‐form and the processed form of MT1‐MMP. Metastasizing HNSCCs showed increased expression of MT1‐MMP. Furthermore, pro‐MT1‐MMP expression was noted in most of the nonmetastasizing HNSCCs analyzed by Western blot, and it was absent in the metastasizing HNSCCs. This finding suggests a lower level of furin‐mediated MT1‐MMP activation in the less aggressive cancers. These observations indicate that furin plays a role in tumor progression. Its overexpression in more aggressive or metastasizing cancers resulted in increased MMP processing. © 2001 Wiley‐Liss, Inc.
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