Division of Endocrinology, Diabetes, and Bone Diseases, Department of Medicine III, Technical University Medical Center, Fetscherstrasse 74, Dresden, Germany.
Eur J Endocrinol. 2011 Dec;165(6):833-40. doi: 10.1530/EJE-11-0454. Epub 2011 Aug 18.
Signalling of receptor activator of nuclear factor-κB (RANK) ligand (RANKL) through RANK is a critical pathway to regulate the differentiation and activity of osteoclasts and, hence, a master regulator of bone resorption. Increased RANKL activity has been demonstrated in diseases characterised by excessive bone loss such as osteoporosis, rheumatoid arthritis and osteolytic bone metastases. The development and approval of denosumab, a fully MAB against RANKL, has heralded a new era in the treatment of bone diseases by providing a potent, targeted and reversible inhibitor of bone resorption. This article summarises the molecular and cellular biology of the RANKL/RANK system and critically reviews preclinical and clinical studies that have established denosumab as a promising novel therapy for metabolic and malignant bone diseases. We will discuss the potential indications for denosumab along with a critical review of safety and analyse its potential within the concert of established therapies.
核因子-κB 受体激活剂配体(RANKL)通过 RANK 的信号转导是调节破骨细胞分化和活性的关键途径,因此是骨吸收的主要调节剂。在以骨质疏松症、类风湿关节炎和溶骨性骨转移等过度骨丢失为特征的疾病中,已经证明 RANKL 活性增加。Denosumab 的开发和批准,一种针对 RANKL 的完全单克隆抗体,通过提供一种有效的、靶向的和可逆的骨吸收抑制剂,为骨疾病的治疗开创了一个新时代。本文总结了 RANKL/RANK 系统的分子和细胞生物学,并对已确立的作为代谢和恶性骨疾病有前途的新型治疗药物的 denosumab 的临床前和临床研究进行了批判性回顾。我们将讨论 denosumab 的潜在适应症,对安全性进行批判性评估,并分析其在既定治疗方案中的潜力。