Sema3A Inhibits Osteolytic Bone Metastasis of Non-small Cell Lung Cancer

IF 2.5 4区 医学 Q3 ONCOLOGY
Wei Wang, Kaicheng Shen, Ruyan Liu, Qi Zhou
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引用次数: 0

Abstract

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.
Sema3A 抑制非小细胞肺癌的骨溶解性骨转移
背景:溶骨性骨转移是非小细胞肺癌(NSCLC)的常见并发症,会导致骨痛、高钙血症和骨折,严重降低患者的生活质量和生存时间。闪形蛋白 3A(Sema3A)是闪形蛋白家族的同工型之一,在血管生成、免疫调节和肿瘤发生等多种生理和病理过程中具有重要作用。然而,Sema3A在NSCLC溶骨性骨转移发生过程中的作用尚不清楚。研究方法本研究建立了模拟 NSCLC 细胞调节成骨细胞和破骨细胞前体分化和成熟的体外模型,并观察了成骨细胞和破骨细胞的分化情况。结果显示结果表明,Sema3A的表达可抑制NSCLC细胞的增殖、迁移和侵袭,促进成骨细胞的分化,抑制破骨细胞的分化,提示Sema3A可抑制NSCLC溶骨性骨转移的发生和发展。结论本研究为临床治疗NSCLC溶骨性骨转移瘤提供了新思路。
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来源期刊
CiteScore
4.50
自引率
7.10%
发文量
55
审稿时长
3 months
期刊介绍: Aims & Scope Recent Patents on Anti-Cancer Drug Discovery publishes review and research articles that reflect or deal with studies in relation to a patent, application of reported patents in a study, discussion of comparison of results regarding application of a given patent, etc., and also guest edited thematic issues on recent patents in the field of anti-cancer drug discovery e.g. on novel bioactive compounds, analogs, targets & predictive biomarkers & drug efficacy biomarkers. The journal also publishes book reviews of eBooks and books on anti-cancer drug discovery. A selection of important and recent patents on anti-cancer drug discovery is also included in the journal. The journal is essential reading for all researchers involved in anti-cancer drug design and discovery. The journal also covers recent research (where patents have been registered) in fast emerging therapeutic areas/targets & therapeutic agents related to anti-cancer drug discovery.
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