Noël A, Gilles C, Bajou K, Devy L, Kebers F, Lewalle J M, Maquoi E, Munaut C, Remacle A, Foidart J M
Laboratory of Tumor and Development Biology, University of Liège, Sart-Tilman, Belgium.
Invasion Metastasis. 1997;17(5):221-39.
Metalloproteinases and serine proteinases have been associated with tumor invasion and formation of metastasis which represent the major obstacles to cancer cure. The contribution of proteinases in these processes was initially thought to be the destruction of extracellular matrices. However, recent evidence suggests that they mainly affect tumor growth rather than invasion. Proteinases can indeed generate active matrix protein fragments, influence the release, the activation and the bioavailability of growth factors, and consequently modulate tumor cell growth, apoptosis and angiogenesis. Additionally, proteinases, their receptors and/or inhibitors can be directly involved in cell migration and in the processing or shedding of cell surface proteins. Further elucidation of the functions of proteinases is essential for the development of novel anticancer strategies.
金属蛋白酶和丝氨酸蛋白酶与肿瘤侵袭及转移形成相关,而肿瘤侵袭和转移是癌症治愈的主要障碍。蛋白酶在这些过程中的作用最初被认为是破坏细胞外基质。然而,最近的证据表明它们主要影响肿瘤生长而非侵袭。蛋白酶确实能够产生活性基质蛋白片段,影响生长因子的释放、激活及生物利用度,进而调节肿瘤细胞的生长、凋亡和血管生成。此外,蛋白酶、其受体和/或抑制剂可直接参与细胞迁移以及细胞表面蛋白的加工或脱落。进一步阐明蛋白酶的功能对于开发新型抗癌策略至关重要。