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Lithium Chloride Suppresses Colorectal Cancer Cell Survival and Proliferation through ROS/GSK-3β/NF-κB Signaling Pathway

机译:氯化锂通过ROS /GSK-3β/NF-κB信号通路抑制大肠癌细胞的存活和增殖

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Glycogen synthase kinase-3β(GSK-3β), a serine/threonine protein kinase, has been regarded as a potential therapeutic target for multiple human cancers. In addition, oxidative stress is closely related to all aspects of cancer. We sought to determine the biological function of lithium, one kind of GSK-3βinhibitors, in the process of reactive oxygen species (ROS) production in colorectal cancer. In this study, we analyzed the cell apoptosis and proliferation by cell viability, EdU, and flow cytometry assays through administration of LiCl. We used polymerase chain reaction and Western blotting to establish the effect of GSK-3βinhibition on the nuclear factor-κB (NF-κB) pathway. Results showed administration of LiCl increased apoptosis and the level of ROS in colorectal cancer cells. Furthermore, the underlying mechanisms could be mediated by the reduction of NF-κB expression and NF-κB-mediated transcription. Taken together, our results demonstrated that therapeutic targeting of ROS/GSK-3β/NF-κB pathways may be an effective way for colorectal cancer intervention, although further preclinical and clinical testing are desirable.
机译:糖原合酶激酶3β(GSK-3β)是一种丝氨酸/苏氨酸蛋白激酶,被认为是多种人类癌症的潜在治疗靶标。此外,氧化应激与癌症的各个方面都息息相关。我们试图确定一种GSK-3β抑制剂锂在结直肠癌中产生活性氧(ROS)的过程中的生物学功能。在这项研究中,我们通过施用LiCl通过细胞活力,EdU和流式细胞术分析了细胞的凋亡和增殖。我们使用聚合酶链反应和蛋白质印迹来建立GSK-3β抑制作用对核因子-κB(NF-κB)途径的影响。结果表明,施用LiCl可以增加大肠癌细胞的凋亡和ROS水平。此外,潜在的机制可以通过减少NF-κB表达和NF-κB介导的转录来介导。两者合计,我们的结果表明,尽管需要进一步的临床前和临床测试,但靶向治疗ROS /GSK-3β/NF-κB途径可能是结肠直肠癌干预的有效途径。

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