4.5 Review

Cell surface-anchored serine proteases in cancer progression and metastasis

期刊

CANCER AND METASTASIS REVIEWS
卷 38, 期 3, 页码 357-387

出版社

SPRINGER
DOI: 10.1007/s10555-019-09811-7

关键词

Type II transmembrane serine proteases; Cancer; Matriptase; Hepsin; TMPRSS2; TMPRSS3; TMPRSS4; Prostasin; Testisin

类别

资金

  1. NIH/NCI [R01CA222359A]
  2. Susan G. Komen [IBC17511329, IBC18511329]
  3. NIH/NCI Training grant [T32-CA009531]

向作者/读者索取更多资源

Over the last two decades, a novel subgroup of serine proteases, the cell surface-anchored serine proteases, has emerged as an important component of the human degradome, and several members have garnered significant attention for their roles in cancer progression and metastasis. A large body of literature describes that cell surface-anchored serine proteases are deregulated in cancer and that they contribute to both tumor formation and metastasis through diverse molecular mechanisms. The loss of precise regulation of cell surface-anchored serine protease expression and/or catalytic activity may be contributing to the etiology of several cancer types. There is therefore a strong impetus to understand the events that lead to deregulation at the gene and protein levels, how these precipitate in various stages of tumorigenesis, and whether targeting of selected proteases can lead to novel cancer intervention strategies. This review summarizes current knowledge about cell surface-anchored serine proteases and their role in cancer based on biochemical characterization, cell culture-based studies, expression studies, and in vivo experiments. Efforts to develop inhibitors to target cell surface-anchored serine proteases in cancer therapy will also be summarized.

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