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首页> 外文期刊>Journal of pharmacological sciences. >2-Aminophenoxazine-3-one Prevents Pulmonary Metastasis of Mouse B16 Melanoma Cells in Mice
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2-Aminophenoxazine-3-one Prevents Pulmonary Metastasis of Mouse B16 Melanoma Cells in Mice

机译:2-Aminophenoxazine-3-one预防小鼠小鼠B16黑色素瘤细胞的肺转移。

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摘要

References(33) Cited-By(4) 2-Aminophenoxazine-3-one (Phx-3) induced cellular apoptosis in mouse melanoma B16 cells as detected by DNA laddering and upregulated Fas expression in the cells in vitro. Next, the anti-metastatic effects of Phx-3 were investigated in C56BL/6 mice. When B16 melanoma cells were injected into the tail veins of mice, significant metastasis of the cells was indicated in the lungs, 14 days after treatment. In contrast, when 0.5 mg/kg Phx-3 was administered to mice through the tail veins, once simultaneously with or every three days after the administration of B16 melanoma cells, the number of metastasized pulmonary cells was extremely reduced. Moderate reduction of the number of metastasized pulmonary cells was indicated in the mice with a single dose of Phx-3 on day 3 after injection of the cells. However, when Phx-3 was administered in a single dose, 6 or 9 days after the injection of the cells, the number of metastasized pulmonary cells remained the same. The present results indicate that the metastasis of mouse B16 melanoma cells to the lung was significantly inhibited in mice administered Phx-3, which activated the intrinsic and extrinsic apoptotic pathways. The present study suggests that Phx-3 might be a potential anti-metastatic agent as well as an anticancer agent.
机译:参考文献(33)被引证的By(4)2-Aminophenoxazine-3-one(Phx-3)诱导小鼠黑素瘤B16细胞凋亡,通过DNA梯形检测和上调Fas在体外的表达。接下来,在C56BL / 6小鼠中研究了Phx-3的抗转移作用。当将B16黑素瘤细胞注射到小鼠的尾静脉中时,在治疗后14天,在肺中表明了细胞的明显转移。相反,当通过尾静脉给小鼠施用0.5mg / kg Phx-3时,与施用B16黑素瘤细胞同时或每三天一次,转移的肺细胞的数量大大减少。在注射细胞后第3天,用单剂量的Phx-3在小鼠中表明转移的肺细胞数量的适度减少。但是,在注射细胞后6或9天以单剂形式服用Phx-3时,转移的肺细胞数量保持不变。目前的结果表明,在施用Phx-3的小鼠中,小鼠B16黑色素瘤细胞向肺的转移受到了显着抑制,从而激活了内在和外在的凋亡途径。本研究表明,Phx-3可能是一种潜在的抗转移药以及一种抗癌药。

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