Genomics & Functional Proteomics Laboratories, Osteoporosis Research Center; Creighton University Medical Center, 601 N 30th Street, Suite 6730, Omaha, NE 68131, USA.
Expert Rev Proteomics. 2010 Feb;7(1):103-11. doi: 10.1586/epr.09.90.
Osteoporosis is prevalent among the elderly and is a major cause of bone fracture in this population. Bone integrity is maintained by the dynamic processes of bone resorption and bone formation (bone remodeling). Osteoporosis results when there is an imbalance of the two counteracting processes. Bone mineral density, measured by dual-energy x-ray absorptiometry has been the primary method to assess fracture risk for decades. Recent studies demonstrated that measurement of bone turnover markers allows for a dynamic assessment of bone remodeling, while imaging techniques, such as dual-energy x-ray absorptiometry, do not. The application of proteomics has permitted discoveries of new, sensitive, bone turnover markers, which provide unique information for clinical diagnosis and treatment of patients with bone diseases. This review summarizes the recent findings of proteomic studies on bone diseases, properties of mesenchymal stem cells with high expansion rates and osteoblast and osteoclast differentiation, with emphasis on the role of quantitative proteomics in the study of signaling dynamics, biomarkers and discovery of therapeutic targets.
骨质疏松症在老年人中很常见,是该人群骨折的主要原因。骨完整性由骨吸收和骨形成(骨重建)的动态过程维持。当两种相互抵消的过程失衡时,就会导致骨质疏松症。双能 X 线吸收法测量的骨矿物质密度已成为数十年来评估骨折风险的主要方法。最近的研究表明,骨转换标志物的测量可以对骨重建进行动态评估,而像双能 X 线吸收法这样的成像技术则不行。蛋白质组学的应用允许发现新的、敏感的骨转换标志物,为骨疾病患者的临床诊断和治疗提供了独特的信息。这篇综述总结了骨疾病的蛋白质组学研究的最新发现,包括具有高扩增率的间充质干细胞和成骨细胞和成骨细胞分化的特性,重点介绍了定量蛋白质组学在研究信号动态、生物标志物和发现治疗靶点方面的作用。