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The Effects of Ultrasound and Arsenic Trioxide on Neurogliocytoma Cells and Secondary Activation of Macrophages

三氧化二砷 细胞凋亡 细胞内 膜联蛋白 超声波 程序性细胞死亡 乳酸脱氢酶 声动力疗法 胶质瘤 分泌物 坏死 微气泡 化学 医学 癌症研究 病理 生物化学 放射科
作者
Yonggang Xu,Yafang Zhang,Xiaoqian Liu,Zhi Wang,Jing Ma,Jie Wang,Yue Wu
出处
期刊:Tumori Journal [SAGE]
卷期号:95 (6): 780-788 被引量:5
标识
DOI:10.1177/030089160909500622
摘要

Aims and Background As a new technique for clinical therapeutics, ultrasound has synergistic effects on traditional chemotherapy. Arsenic trioxide (AS 2 O 3 ), an apoptosis-inducing drug, has successfully been used in the treatment of some tumor types in recent years. Macrophages have both positive and negative effects on the occurrence and development of tumors. The aim of this study was to observe the effects of ultrasound and AS 2 O 3 on a glioma cell line and the secondary activation of macrophages by cell death, in order to provide a theoretical basis for the clinical application of AS 2 O 3 and ultrasound in glioma treatment. Methods Different AS 2 O 3 concentrations were used solely or combined with ultrasound in rat glioma C6 cells to induce cell death. The degree of C6 cell death was determined by AnnexinV-FITC and PI double staining. The intracellular arsenium concentration and the release of lactate dehydrogenase (LDH) from C6 cells were also measured. The supernatant of C6 cells was then used to stimulate macrophages. Finally the activation of NF-κB and the secretion of TNF-α and TGF-β1 by macrophages were determined. Results The cell death increase in the group where ultrasound was used together with AS 2 O 3 was significantly higher than that obtained by either ultrasound or AS 2 O 3 . The increase was also significantly higher than the sum of the increases in the ultrasound and the AS 2 O 3 only groups. At the same AS 2 O 3 concentration, additional treatment with ultrasound can significantly increase the intracellular arsenium concentration. The release of LDH from C6 cells showed a close, direct correlation with late apoptosis and necrosis, but did not exhibit an obvious correlation with early apoptosis. The activation of NF-κB and the secretion of TNF-α and TGF-β1 in macrophages also showed a close direct correlation with late apoptosis and necrosis. Conclusions This in vitro study demonstrates that ultrasound may synergistically enhance the cell-killing effect by promoting AS 2 O 3 to enter the C6 cells. Macrophages may be activated by killed C6 cells, especially by necrotic C6 cells.
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