Reid Penny, Holen Ingunn
Academic Unit of Clinical Oncology, School of Medicine and Biomedical Sciences, University of Sheffield, Beech Hill Road, Sheffield S10 5RX, UK.
Eur J Cell Biol. 2009 Jan;88(1):1-17. doi: 10.1016/j.ejcb.2008.06.004. Epub 2008 Aug 15.
Osteoprotegerin (OPG) is a secreted glycoprotein central to bone turnover via its role as a decoy receptor for the receptor activator of nuclear factor kappaB ligand (RANKL) and has traditionally been linked to a number of bone-related diseases. However, there is additional evidence that OPG can promote cell survival by inhibiting TNF-related apoptosis-inducing ligand (TRAIL)-induced apoptosis. As a result, a number of in vitro, in vivo and clinical studies have been performed assessing the role of OPG in tumourigenesis. Similar studies have been performed regarding vascular pathologies, resulting from observations of expression and regulation of OPG in the vasculature. This review aims to provide an update on this area and assess the potential protective or detrimental role of OPG in both vascular pathologies and tumourigenesis.
骨保护素(OPG)是一种分泌型糖蛋白,通过作为核因子κB受体活化因子配体(RANKL)的诱饵受体,在骨转换中起核心作用,传统上它与多种骨相关疾病有关。然而,有更多证据表明,OPG可通过抑制肿瘤坏死因子相关凋亡诱导配体(TRAIL)诱导的凋亡来促进细胞存活。因此,已经进行了许多体外、体内和临床研究,以评估OPG在肿瘤发生中的作用。关于血管病变也进行了类似的研究,这是基于对血管系统中OPG表达和调控的观察。本综述旨在提供该领域的最新进展,并评估OPG在血管病变和肿瘤发生中潜在的保护或有害作用。