Department of Pharmacology, Wayne State University School of Medicine, Gordon H. Scott Hall of Basic Medical Sciences, Room 6332, 540 East Canfield, Detroit, MI, 48201, USA.
Department of Oncology, Wayne State University and Barbara Ann Karmanos Cancer Institute, Gordon H. Scott Hall of Basic Medical Sciences, Room 6332, 540 East Canfield, Detroit, MI, 48201, USA.
Cancer Metastasis Rev. 2019 Sep;38(3):357-387. doi: 10.1007/s10555-019-09811-7.
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.
在过去的二十年中,一类新型的丝氨酸蛋白酶——细胞表面锚定丝氨酸蛋白酶,已成为人类降解组的重要组成部分,其中一些成员因其在癌症进展和转移中的作用而受到广泛关注。大量文献描述了细胞表面锚定丝氨酸蛋白酶在癌症中的失调现象,它们通过多种分子机制促进肿瘤的形成和转移。细胞表面锚定丝氨酸蛋白酶表达和/或催化活性的精确调控丧失可能是导致多种癌症类型发生的原因之一。因此,人们强烈希望了解导致基因和蛋白质水平失调的事件,以及这些事件如何在肿瘤发生的各个阶段发生,并确定是否可以针对特定的蛋白酶来制定新的癌症干预策略。本综述基于生化特征、基于细胞培养的研究、表达研究和体内实验,总结了细胞表面锚定丝氨酸蛋白酶及其在癌症中的作用的现有知识。还将总结开发抑制剂以靶向癌症治疗中细胞表面锚定丝氨酸蛋白酶的相关努力。