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氯化锂对白血病THP-1细胞生长的抑制作用及其对Wnt通路的影响[J]. 肿瘤防治研究, 2014, 41(06): 568-572. DOI: 10.3971/j.issn.1000-8578.2014.06.013
引用本文: 氯化锂对白血病THP-1细胞生长的抑制作用及其对Wnt通路的影响[J]. 肿瘤防治研究, 2014, 41(06): 568-572. DOI: 10.3971/j.issn.1000-8578.2014.06.013
Lithium Chloride Inhibits Proliferation of THP-1 Leukemia Cells and Activates Wnt Signaling Pathway[J]. Cancer Research on Prevention and Treatment, 2014, 41(06): 568-572. DOI: 10.3971/j.issn.1000-8578.2014.06.013
Citation: Lithium Chloride Inhibits Proliferation of THP-1 Leukemia Cells and Activates Wnt Signaling Pathway[J]. Cancer Research on Prevention and Treatment, 2014, 41(06): 568-572. DOI: 10.3971/j.issn.1000-8578.2014.06.013

氯化锂对白血病THP-1细胞生长的抑制作用及其对Wnt通路的影响

Lithium Chloride Inhibits Proliferation of THP-1 Leukemia Cells and Activates Wnt Signaling Pathway

  • 摘要: 摘 要:目的 研究氯化锂(LiCl)在体外对白血病细胞THP-1增殖、凋亡、周期以及Wnt通路的影响。 方法 氯化锂不同浓度不同时间作用THP-1细胞后,用MTT法检测细胞增殖,流式细胞术检测细胞凋亡和周期分布,Western blot检测细胞内Wnt通路的变化。 结果 氯化锂能抑制白血病THP-1细胞的增殖,诱导细胞凋亡,使细胞周期阻滞于G2/M期,且均呈浓度和时间依赖性。氯化锂不同浓度不同时间作用THP-1细胞后,t-GSK3β、cyclinD1表达不变,p-GSK3β、β-catenin表达升高,短时间低浓度作用后c-myc表达升高,但随作用时间延长和浓度增加,c-myc表达降低。 结论 氯化锂对THP-1 细胞有显著的增殖抑制、凋亡诱导、细胞G2/M期阻滞作用,并激活Wnt通路,影响Wnt通路下游蛋白c-myc、cyclinD1的表达。

     

    Abstract: Objective To explore the effects of Lithium Chloride (LiCl) on proliferation, apoptosis and cell cycle of leukemia cells THP-1, and to investigate its effect on Wnt signaling pathway. Methods THP-1 cells were treated with LiCl at different concentrations and time. The proliferation inhibitory rates of THP-1 cells were assayed by MTT. The apoptosis rates and the cell cycle distribution were detected by fl ow cytometry. The expressions of Wnt signaling pathway proteins were analyzed by Western blot. Results LiCl could inhibit the proliferation and induce the apoptosis of THP-1 cells. LiCl mainly arrested THP-1 cells in the G2/M phase in a time- and dose-dependent manner. Western blot results suggested that the expressions of t-GSK3β and cyclinD1 had no obvious change. The expressions of p-GSK3β and β-catenin were increased. The expression of c-myc protein was increased with short-time and low-concentration treatment, while decreased with long-time and high-concentration treatment. Conclusion LiCl could inhibit proliferation, induce apoptosis and arrest cell cycle of THP-1 cells. In addition, it could activate Wnt signaling pathway, and infl uence the expressions of c-myc and cyclinD1 proteins.

     

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