破骨细胞
信号灯
转移
塞马3A
骨溶解
癌症研究
骨转移
成骨细胞
医学
肺癌
血管生成
病理
癌症
生物
内科学
体外
受体
生物化学
外科
作者
Wei Wang,Kaicheng Shen,Ruyan Liu,Qi Zhou
出处
期刊:Recent Patents on Anti-cancer Drug Discovery
[Bentham Science]
日期:2024-04-15
卷期号:19
标识
DOI:10.2174/0115748928295263240402085411
摘要
Background: Osteolytic bone metastasis is a common complication of Non-Small Cell Lung Cancer (NSCLC), resulting in bone pain, hypercalcemia, and fractures that severely reduce the quality of life and survival time of patients. Semaphorins 3A (Sema3A) is one of the isoforms of the Semaphorins family, which is important in a variety of physiological and pathological processes, such as angiogenesis, immune regulation, and tumorigenesis. However, the role of Sema3A in the development of osteolytic bone metastasis in NSCLC is unknown. Methods: In this study, we established in vitro models simulating NSCLC cells in regulating the differentiation and maturation of osteoblast and osteoclast precursors and observed the differentiation of osteoblasts and osteoclasts. Results: The results demonstrated that the expression of Sema3A inhibited the proliferation, migration, and invasion of NSCLC cells, as well as promoted the differentiation of osteoblasts and inhibited the differentiation of osteoclasts, suggesting that Sema3A can inhibit the occurrence and development of osteolytic bone metastasis of NSCLC. Conclusion: This study provides a new idea for the clinical treatment of osteolytic bone metastasis in NSCLC.
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