Hellenic Army Academy, Vari, Greece.
NovaMechanics Ltd, Nicosia, Cyprus.
Curr Top Med Chem. 2018;18(8):661-673. doi: 10.2174/1568026618666180607084430.
The overexpression of Tumor Necrosis Factor (TNF) is directly related to the development of several autoimmune diseases, such as rheumatoid and psoriatic arthritis, inflammatory bowel disease, Crohn's disease, refractory asthma, and multiple sclerosis. Receptor Activator of Nuclear Factor Kappa- B Ligand (RANKL) belongs to the TNF family and is the primary mediator of osteoclast-induced bone resorption through interaction with its receptor RANK. The function of RANKL is physiologically inhibited by the action of osteoprotegerin (OPG), which is a decoy receptor that binds to RANKL and prevents the process of osteoclastogenesis. Malfunction among RANK/RANKL/OPG can also result in bone loss diseases, including postmenopausal osteoporosis, rheumatoid arthritis, bone metastasis and multiple myeloma. To disrupt the unwanted functions of TNF and RANKL, current attempts focus on blocking TNF and RANKL binding to their receptors. In this review, we present the research efforts toward the development of low-molecular-weight pharmaceuticals that directly block the detrimental actions of TNF and RANKL.
肿瘤坏死因子(TNF)的过度表达与几种自身免疫性疾病的发展直接相关,如类风湿关节炎和银屑病关节炎、炎症性肠病、克罗恩病、难治性哮喘和多发性硬化症。核因子κB 受体激活剂配体(RANKL)属于 TNF 家族,通过与其受体 RANK 的相互作用,是破骨细胞诱导骨吸收的主要介质。骨保护素(OPG)的作用可生理性抑制 RANKL 的功能,OPG 是一种诱饵受体,与 RANKL 结合并阻止破骨细胞生成过程。RANK/RANKL/OPG 的功能障碍也会导致骨丢失疾病,包括绝经后骨质疏松症、类风湿关节炎、骨转移和多发性骨髓瘤。为了破坏 TNF 和 RANKL 的不必要功能,目前的尝试集中在阻断 TNF 和 RANKL 与其受体的结合。在这篇综述中,我们介绍了开发直接阻断 TNF 和 RANKL 有害作用的低分子量药物的研究进展。