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首页> 外文期刊>EXCLI Journal >Bioinformatics and experimental studies of anti-leukemic activity from 6-gingerol demonstrate its role in p53 mediated apoptosis pathway
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Bioinformatics and experimental studies of anti-leukemic activity from 6-gingerol demonstrate its role in p53 mediated apoptosis pathway

机译:来自6-gingerol的抗白血病活性的生物信息和实验研究证明了其在P53介导的凋亡途径中的作用

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6-gingerol is a traditional medicine that possesses anti-cancer activity against several types of cancer. However, the mechanism of action still remains unclear. Therefore, this study explored the effects of 6-gingerol on anti-leukemic mechanisms in NB4, MOLT4, and Raji leukemic cell. Results indicated that 6-gingerol inhibited cell proliferation and induced cell apoptosis in these 3 cell lines. Moreover, 6-gingerol was shown to increase the mRNA expression of the caspase family thereby suggesting that 6-gingerol induced apoptosis through the caspase-dependent pathway. To explore the signaling pathway regulating 6-gingerol induced apoptosis, we utilized and integrated the network pharmacology approach together with experimental investigations. Targets of 6-gingerol were identified from ChEMBL and STITCH databases, which were used for constructing the protein-protein interaction (PPI) network. Results from the PPI network indicated that p53 was a key regulator. Moreover, it was found that 6-gingerol could increase the levels of p53 mRNA in all leukemic cell lines. Thus, 6-gingerol has shown to have anti-cancer activity. In addition, p53, BAX and BCL2 could be involved in the apoptosis pathway of these leukemic cells. This study is anticipated to be useful for the development of 6-gingerol as an anti-leukemic drug in the future.
机译:6-gingerol是一种传统药物,具有针对几种癌症的抗癌活动。然而,行动机制仍然尚不清楚。因此,本研究探讨了6-姜醇对NB4,Molt4和Raji白血病细胞抗白血病机制的影响。结果表明,6种细胞抑制细胞增殖和诱导细胞凋亡在这些3细胞中。此外,示出了6-姜醇,增加了胱天蛋白酶系列的mRNA表达,从而提示通过依赖于胱天蛋白酶依赖性途径诱导6-姜醇诱导的细胞凋亡。为了探索调节6-姜醇诱导细胞凋亡的信号通路,我们利用和整合网络药理学方法以及实验研究。从ChemBL和针脚数据库中鉴定了6-姜醇的靶标,其用于构建蛋白质 - 蛋白质相互作用(PPI)网络。 PPI网络的结果表明P53是关键调节器。此外,发现6-姜醇可以增加所有白血病细胞系中p53 mRNA的水平。因此,6-姜醇显示出具有抗癌活动。此外,P53,BAX和BCL2可参与这些白血病细胞的凋亡途径。预计本研究将在未来的抗白血病药物中发育6-geringer。

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