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首页> 外文期刊>Dermatology: international journal for clinical and investigative dermatology >ING4 Inhibits Proliferation and Induces Apoptosis in Human Melanoma A375 Cells via the Fas/Caspase-8 Apoptosis Pathway
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ING4 Inhibits Proliferation and Induces Apoptosis in Human Melanoma A375 Cells via the Fas/Caspase-8 Apoptosis Pathway

机译:ING4通过Fas / Caspase-8细胞凋亡途径抑制人黑素瘤A375细胞的增殖并诱导其细胞凋亡

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摘要

Background: Inhibitor of growth 4 (ING4) plays a role in regulating the cell cycle, apoptosis, cell invasion and migration, but the mechanisms involved remain to be elucidated. Objective: To explore how ING4 affects human malignant melanoma A375 cells. Methods: Recombinant lentiviral vectors (A375/pLenO-GTP-ING4) were constructed and transfected into A375 cells (experimental group). The impact of ING4 on the proliferation and apoptosis of A375 cells was investigated in in vitro and in vivo experiments in mice using the MTT assay and flow cytometry. Results: In the experimental group, optical density was lower and apoptotic cells were more frequent from days 2-5 (p = 0.000 and p < 0.01); there were smaller xenografts and more apoptotic cells in mice (all p < 0.05); moreover, increased levels of Fas, cleaved caspase-8 and caspase-3, and decreased levels of FasL and procyclic acidic repetitive protein were observed in vitro and in vivo. Conclusion: ING4 might suppress proliferation and enhance apoptosis in human malignant melanoma cells by activating Fas-induced apoptosis in a caspase-8-dependent pathway. (C) 2016 S. Karger AG, Basel
机译:背景:生长抑制剂4(ING4)在调节细胞周期,凋亡,细胞侵袭和迁移中发挥作用,但涉及的机制仍有待阐明。目的:探讨ING4如何影响人恶性黑色素瘤A375细胞。方法:构建重组慢病毒载体(A375 / pLenO-GTP-ING4)并将其转染到A375细胞(实验组)中。使用MTT测定法和流式细胞术在小鼠体内和体外实验中研究了ING4对A375细胞增殖和凋亡的影响。结果:在实验组中,从第2天到第5天,光密度较低,凋亡细胞更为频繁(p = 0.000和p <0.01);小鼠的异种移植物较小,凋亡细胞更多(所有p <0.05);此外,在体外和体内均观察到Fas水平升高,caspase-8和caspase-3裂解,以及FasL和脯氨酸酸性重复蛋白水平降低。结论:ING4可能通过激活Fas诱导的caspase-8依赖性细胞凋亡来抑制人恶性黑色素瘤细胞的增殖并增强其凋亡。 (C)2016 S.Karger AG,巴塞尔

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