骨质疏松症
骨转移
医学
乳腺癌
转移
细胞外基质
骨组织
骨愈合
癌症研究
癌症
内科学
病理
外科
生物
细胞生物学
作者
Sunghan Lee,Y. Kim,Hyo‐Il Jung,Ji Seok Lim,Ki‐Chang Nam,Han Seok Choi,Bong Seop Kwak
出处
期刊:Biofabrication
[IOP Publishing]
日期:2024-08-08
卷期号:16 (4): 045025-045025
被引量:1
标识
DOI:10.1088/1758-5090/ad6cf9
摘要
Osteoporosis is the most common bone disorder, which is a highly dangerous condition that can promote bone metastases. As the current treatment for osteoporosis involves long-term medication therapy and a cure for bone metastasis is not known, ongoing efforts are required for drug development for osteoporosis. Animal experiments, traditionally used for drug development, raise ethical concerns and are expensive and time-consuming. Organ-on-a-chip technology is being developed as a tool to supplement such animal models. In this study, we developed a bone-on-a-chip by co-culturing osteoblasts, osteocytes, and osteoclasts in an extracellular matrix environment that can represent normal bone, osteopenia, and osteoporotic conditions. We then simulated bone metastases using breast cancer cells in three different bone conditions and observed that bone metastases were most active in osteoporotic conditions. Furthermore, it was revealed that the promotion of bone metastasis in osteoporotic conditions is due to increased vascular permeability. The bone-on-a-chip developed in this study can serve as a platform to complement animal models for drug development for osteoporosis and bone metastasis.
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