Division of Materials and Manufacturing Science, Graduate School of Engineering, Osaka University, 2-1 Yamada-oka, Suita, Osaka 565-0871, Japan.
Teijin Nakashima Medical Co. Ltd., 688-1, Joto-Kitagata, Higashi-ku, Okayama 709-0625, Japan.
Biomolecules. 2021 Jan 20;11(2):131. doi: 10.3390/biom11020131.
Malignant melanoma favors spreading to bone, resulting in a weakened bone with a high fracture risk. Here, we revealed the disorganized alignment of apatite crystals in the bone matrix associated with the homing of cancer cells by developing an artificially controlled ex vivo melanoma bone metastasis model. The ex vivo metastasis model reflects the progressive melanoma cell activation in vivo, resulting in decreased bone mineral density and expression of MMP1-positive cells. Moreover, less organized intercellular connections were observed in the neighboring osteoblasts in metastasized bone, indicating the abnormal and randomized organization of bone matrix secreted by disconnected osteoblasts. Our study revealed that the deteriorated microstructure associated with disorganized osteoblast arrangement was a determinant of malignant melanoma-related bone dysfunction.
恶性黑色素瘤易于扩散至骨骼,导致骨质脆弱,骨折风险增加。在这里,我们通过建立一种人为控制的体外黑色素瘤骨转移模型,揭示了与癌细胞归巢相关的骨基质中磷灰石晶体排列紊乱的现象。该体外转移模型反映了体内黑色素瘤细胞的逐渐激活,导致骨密度降低和 MMP1 阳性细胞表达增加。此外,在转移骨中相邻成骨细胞中观察到细胞间连接减少,表明由脱偶联成骨细胞分泌的骨基质的排列异常和随机化。我们的研究表明,与成骨细胞排列紊乱相关的恶化的微观结构是恶性黑色素瘤相关骨功能障碍的决定因素。