| Literature DB >> 33498283 |
Aira Matsugaki1, Yumi Kimura1, Ryota Watanabe1,2, Fumihito Nakamura1, Ryo Takehana1, Takayoshi Nakano1.
Abstract
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.Entities:
Keywords: bone tissue microstructure; ex vivo metastasis model; malignant melanoma; osteoblast
Year: 2021 PMID: 33498283 PMCID: PMC7909255 DOI: 10.3390/biom11020131
Source DB: PubMed Journal: Biomolecules ISSN: 2218-273X