Bach Leon A
Department of Medicine (Alfred), Monash University, Prahran, 3181, Australia,
J Cell Commun Signal. 2015 Jun;9(2):189-200. doi: 10.1007/s12079-015-0288-4. Epub 2015 Mar 26.
IGFBP-6 is an O-linked glycoprotein that preferentially binds IGF-II over IGF-I. It is a relatively selective inhibitor of IGF-II actions including proliferation, survival and differentiation of a wide range of cells. IGFBP-6 has recently been shown to have a number of IGF-independent actions, including promotion of apoptosis in some cells and inhibition of angiogenesis. IGFBP-6 also induces migration of tumour cells including rhabdomyosarcomas by an IGF-independent mechanism. This chemotactic effect is mediated by MAP kinases. IGFBP-6 binds to prohibitin-2 on the cell surface and the latter is required for IGFBP-6-induced migration by a mechanism that is independent of MAP kinases. IGFBP-6 may enter the nucleus and modulate cell survival and differentiation. IGFBP-6 expression is decreased in a number of cancer cells and it has been postulated to act as a tumour suppressor. IGFBP-6 expression is increased in a smaller number of cancers, which may reflect a compensatory mechanism to control IGF-II actions or IGF-independent actions. The relative balance of IGF-dependent and IGF-independent actions of IGFBP-6 in vivo together with the related question regarding the roles of IGFBP-6 binding to IGF and non-IGF ligands are keys to understanding the physiological role of this protein.
胰岛素样生长因子结合蛋白6(IGFBP - 6)是一种O - 连接糖蛋白,与胰岛素样生长因子II(IGF - II)的结合优先于胰岛素样生长因子I(IGF - I)。它是IGF - II作用的相对选择性抑制剂,这些作用包括多种细胞的增殖、存活和分化。最近研究表明,IGFBP - 6具有许多不依赖IGF的作用,包括促进某些细胞的凋亡和抑制血管生成。IGFBP - 6还通过一种不依赖IGF的机制诱导肿瘤细胞迁移,包括横纹肌肉瘤细胞。这种趋化作用由丝裂原活化蛋白激酶(MAP激酶)介导。IGFBP - 6与细胞表面的抑制素 - 2结合,而后者是IGFBP - 6诱导迁移所必需的,其机制独立于MAP激酶。IGFBP - 6可能进入细胞核并调节细胞存活和分化。在许多癌细胞中IGFBP - 6表达降低,据推测它起着肿瘤抑制因子的作用。在较少数量的癌症中IGFBP - 6表达增加,这可能反映了一种控制IGF - II作用或不依赖IGF作用的补偿机制。IGFBP - 6在体内依赖IGF和不依赖IGF作用的相对平衡,以及关于IGFBP - 6与IGF及非IGF配体结合作用的相关问题,是理解该蛋白生理作用的关键。