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小分子化合物PHA-767491对白血病K562细胞抑制增殖和诱导凋亡的作用[J]. 肿瘤防治研究, 2015, 42(03): 238-241. DOI: 10.3971/j.issn.1000-8578.2015.03.006
引用本文: 小分子化合物PHA-767491对白血病K562细胞抑制增殖和诱导凋亡的作用[J]. 肿瘤防治研究, 2015, 42(03): 238-241. DOI: 10.3971/j.issn.1000-8578.2015.03.006
PHA-767491 Inhibits Proliferation and Induces Apoptosis of Leukemia Cells K562[J]. Cancer Research on Prevention and Treatment, 2015, 42(03): 238-241. DOI: 10.3971/j.issn.1000-8578.2015.03.006
Citation: PHA-767491 Inhibits Proliferation and Induces Apoptosis of Leukemia Cells K562[J]. Cancer Research on Prevention and Treatment, 2015, 42(03): 238-241. DOI: 10.3971/j.issn.1000-8578.2015.03.006

小分子化合物PHA-767491对白血病K562细胞抑制增殖和诱导凋亡的作用

PHA-767491 Inhibits Proliferation and Induces Apoptosis of Leukemia Cells K562

  • 摘要: 目的 探讨PHA-767491对白血病细胞K562的抑制能力及分子机制。方法 采用不同浓度的PHA-767491作用于K562细胞,利用MTT法在不同的时间点检测细胞存活率,RT-PCR及Western blot检测PHA-767491诱导的凋亡信号途径,hochest染色及流式细胞术检测K562的凋亡水平。结果 PHA-767491显著抑制K562细胞的增殖,进一步结果表明PHA-767491可以显著下调抗凋亡蛋白Xiap和Mcl-1蛋白的表达水平,诱导K562细胞通过Caspase途径进入凋亡。结论 PHA-767491可以通过诱导K562细胞凋亡而显著抑制其增殖,为今后的白血病治疗提供了一种新的备选药物。

     

    Abstract: Objective To explore the anti-tumor effect and the mechanism of PHA-767491 against leukemia cells K562. Methods After different concentration of PHA-767491 acted on K562 cells, cell survival rate was detected by MTT at different time, the apoptosis signal pathway was examined by RT-PCR and Western blot, and cell apoptosis was checked by hochest staining and flow cytometry. Results PHA-767491 inhibited the proliferation of K562 cells significantly, by the way of reducing the expression levels of antiapoptotic protein Xiap and Mcl-1 significantly, and inducing cell apoptosis through Caspase pathway. Conclusion PHA-767491 could inhibit the proliferation of K562 cells significantly through inducing cell apoptosis, thus, it could be a new alternative leukemia drug in the future.

     

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