Department of Bone Tumor Surgery, Changzheng Hospital, Second Military Medical University, Shanghai, China.
Division of Rheumatology, Zhongda Hospital, Dongnan University, Nanjing, China.
Biochem Biophys Res Commun. 2014 Jan 17;443(3):944-9. doi: 10.1016/j.bbrc.2013.12.075. Epub 2013 Dec 19.
Giant cell tumor (GCT) of bone is an aggressive skeletal tumor characterized by localized bone resorption. Matrix metalloproteinase-13 (MMP-13) is the principal proteinase expressed by the stromal cells of GCT (GCTSCs) and also considered to play a crucial role in formation of the osteolytic lesion in GCT. However, the exact mechanism of the regulation of MMP-13 expression in GCTSCs was unknown. In this study, we identified miR-126-5p was significantly downregulated in GCTSCs and affect osteoclast (OC) differentiation and bone resorption by repressing MMP-13 expression at the post-transcriptional level. Thus, our studies show that miR-126-5p plays an important physiological role in multinucleated giant cell formation and osteolytic lesion in GCT.
骨巨细胞瘤(GCT)是一种侵袭性骨骼肿瘤,其特征为局部骨质吸收。基质金属蛋白酶-13(MMP-13)是 GCT 基质细胞(GCTSCs)表达的主要蛋白酶,也被认为在 GCT 的溶骨性病变形成中发挥关键作用。然而,GCTSCs 中 MMP-13 表达的调控的确切机制尚不清楚。在这项研究中,我们发现 miR-126-5p 在 GCTSCs 中显著下调,并通过在转录后水平抑制 MMP-13 的表达来影响破骨细胞(OC)分化和骨质吸收。因此,我们的研究表明 miR-126-5p 在 GCT 中的多核巨细胞形成和溶骨性病变中发挥重要的生理作用。