Clément-Demange Lise, Clézardin Philippe
INSERM, UMR 1033, Lyon F-69372, France; Université Lyon-1, Villeurbanne F-69622, France.
INSERM, UMR 1033, Lyon F-69372, France; Université Lyon-1, Villeurbanne F-69622, France.
Curr Opin Pharmacol. 2015 Jun;22:79-86. doi: 10.1016/j.coph.2015.04.004. Epub 2015 May 14.
Skeletal lesions contribute substantially to morbidity and mortality in patients with cancer. Emerging treatments for metastatic bone disease have arisen from our understanding of the biology of bone metastases. Tumour cells alter the functions of bone-resorbing (osteoclasts) and bone-forming (osteoblasts) cells, promoting skeletal destruction. Drugs that inhibit osteoclast-mediated bone resorption (denosumab, bisphosphonates) are the standard of care for patients with skeletal metastases. In this review, we describe the progress and future directions of novel bone-targeted therapies that not only focus on osteoclasts, but also on osteoblasts and the bone microenvironment.
骨骼病变在癌症患者的发病和死亡中起着重要作用。转移性骨病的新兴治疗方法源于我们对骨转移生物学的理解。肿瘤细胞改变了骨吸收(破骨细胞)和成骨(成骨细胞)细胞的功能,促进骨骼破坏。抑制破骨细胞介导的骨吸收的药物(地诺单抗、双膦酸盐)是骨转移患者的标准治疗方法。在本综述中,我们描述了新型骨靶向治疗的进展和未来方向,这些治疗不仅关注破骨细胞,还关注成骨细胞和骨微环境。