Kazerounian S, Yee K O, Lawler J
Division of Cancer Biology and Angiogenesis, Department of Pathology, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachussetts 02215, USA.
Cell Mol Life Sci. 2008 Mar;65(5):700-12. doi: 10.1007/s00018-007-7486-z.
The thrombospondins (TSPs) are a family of five proteins that are involved in the tissue remodeling that is associated with embryonic development, wound healing, synaptogenesis, and neoplasia. These proteins mediate the interaction of normal and neoplastic cells with the extracellular matrix and surrounding tissue. In the tumor microenvironment, TSP-1 has been shown to suppress tumor growth by inhibiting angiogenesis and by activating transforming growth factor beta. TSP-1 inhibits angiogenesis through direct effects on endothelial cell migration and survival, and through effects on vascular endothelial cell growth factor bioavailability. In addition, TSP-1 may affect tumor cell function through interaction with cell surface receptors and regulation of extracellular proteases. Whereas the role of TSP-1 in the tumor microenvironment is the best characterized, the other TSPs may have similar functions. (Part of a Multi-author Review).
血小板反应蛋白(TSPs)是一个由五种蛋白质组成的家族,它们参与了与胚胎发育、伤口愈合、突触形成和肿瘤形成相关的组织重塑过程。这些蛋白质介导正常细胞和肿瘤细胞与细胞外基质及周围组织的相互作用。在肿瘤微环境中,TSP-1已被证明可通过抑制血管生成和激活转化生长因子β来抑制肿瘤生长。TSP-1通过对内皮细胞迁移和存活的直接作用以及对血管内皮细胞生长因子生物利用度的影响来抑制血管生成。此外,TSP-1可能通过与细胞表面受体的相互作用和细胞外蛋白酶的调节来影响肿瘤细胞功能。虽然TSP-1在肿瘤微环境中的作用最为明确,但其他TSPs可能具有类似的功能。(多作者综述的一部分)