Kristensen Ida B, Christensen Jacob Haaber, Lyng Maria B, Møller Michael B, Pedersen Lise, Rasmussen Lars M, Ditzel Henrik J, Abildgaard Niels
Department of Hematology.
Leuk Lymphoma. 2014 Apr;55(4):911-9. doi: 10.3109/10428194.2013.820288. Epub 2013 Aug 5.
Multiple myeloma (MM) lytic bone disease (LBD) is caused by osteoclast activation and osteoblast inhibition. RANK/RANKL/OPG play central roles in osteoclast activation and Wnt inhibitor DKK1 in osteoblast inhibition. The role of other Wnt inhibitors is less clear. We evaluated gene expression of osteoclast regulators (RANK, RANKL, OPG, TRAIL, MIP1A), Wnt inhibitors (DKK1, SFRP2, SFRP3, sclerostin, WIF1) and osteoblast transcription factors (RUNX2, osterix) by quantitative reverse transcriptase polymerase chain reaction (RT-PCR) in the bone marrow (BM) microenvironment using snap-frozen BM biopsies, thereby achieving minimal post-sampling manipulation, and gene expression profiling (GEP) data, reflecting the in vivo situation. We analyzed 110 biopsies from newly diagnosed patients with MM and monoclonal gammopathy of unknown significance (MGUS) and healthy volunteers. LBD was evaluated using standard radiographs and the bone resorption marker CTX-1. Protein levels were evaluated by enzyme-linked immunosorbent assay (ELISA) and immunohistochemistry. Among Wnt inhibitors, only SFRP3 and DKK1 were significantly overexpressed in advanced LBD, correlating with protein levels. SFRP3 correlated with CTX-1. Our findings support osteoblast inhibition as the driving force behind MM LBD.
多发性骨髓瘤(MM)溶骨性骨病(LBD)是由破骨细胞激活和成骨细胞抑制引起的。RANK/RANKL/OPG在破骨细胞激活中起核心作用,而Wnt抑制剂DKK1在成骨细胞抑制中起作用。其他Wnt抑制剂的作用尚不清楚。我们使用速冻骨髓活检,通过定量逆转录聚合酶链反应(RT-PCR)评估骨髓(BM)微环境中破骨细胞调节因子(RANK、RANKL、OPG、TRAIL、MIP1A)、Wnt抑制剂(DKK1、SFRP2、SFRP3、硬化蛋白、WIF1)和成骨细胞转录因子(RUNX2、osterix)的基因表达,从而实现最小化的采样后操作,并获得反映体内情况的基因表达谱(GEP)数据。我们分析了110例新诊断的MM患者、意义未明的单克隆丙种球蛋白病(MGUS)患者和健康志愿者的活检样本。使用标准X线片和骨吸收标志物CTX-1评估LBD。通过酶联免疫吸附测定(ELISA)和免疫组织化学评估蛋白水平。在Wnt抑制剂中,只有SFRP3和DKK1在晚期LBD中显著过表达,与蛋白水平相关。SFRP3与CTX-1相关。我们的研究结果支持成骨细胞抑制是MM LBD背后的驱动力。