Murray Andrew S, Varela Fausto A, List Karin
Biol Chem. 2016 Sep 1;397(9):815-26. doi: 10.1515/hsz-2016-0131.
Carcinogenesis is accompanied by increased protein and activity levels of extracellular cell-surface proteases that are capable of modifying the tumor microenvironment by directly cleaving the extracellular matrix, as well as activating growth factors and proinflammatory mediators involved in proliferation and invasion of cancer cells, and recruitment of inflammatory cells. These complex processes ultimately potentiate neoplastic progression leading to local tumor cell invasion, entry into the vasculature, and metastasis to distal sites. Several members of the type II transmembrane serine protease (TTSP) family have been shown to play critical roles in cancer progression. In this review the knowledge collected over the past two decades about the molecular mechanisms underlying the pro-cancerous properties of selected TTSPs will be summarized. Furthermore, we will discuss how these insights may facilitate the translation into clinical settings in the future by specifically targeting TTSPs as part of novel cancer treatment regimens.
致癌过程伴随着细胞外细胞表面蛋白酶的蛋白质和活性水平升高,这些蛋白酶能够通过直接切割细胞外基质来改变肿瘤微环境,还能激活参与癌细胞增殖、侵袭以及炎症细胞募集的生长因子和促炎介质。这些复杂过程最终会促进肿瘤进展,导致局部肿瘤细胞侵袭、进入脉管系统并转移至远处部位。II型跨膜丝氨酸蛋白酶(TTSP)家族的几个成员已被证明在癌症进展中起关键作用。在本综述中,将总结过去二十年中收集到的关于选定TTSPs促癌特性潜在分子机制的知识。此外,我们将讨论这些见解如何通过将TTSPs作为新型癌症治疗方案的一部分进行特异性靶向,从而在未来促进向临床应用的转化。