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机构地区:[1]中南大学湘雅二医院血液科,长沙410011 [2]泰州市人民医院血液科,江苏泰州225300 [3]山东省立医院血液科 [4]北京珅奥基医药科技有限公司
出 处:《临床血液学杂志》2009年第5期485-487,共3页Journal of Clinical Hematology
摘 要:目的:观察淫羊藿提取物IC163对K562白血病细胞是否具有增殖抑制和诱导凋亡作用。方法:用MTT实验观察不同浓度的IC163对K562细胞增殖抑制率的影响,用Hochest33258染色法和Annexin V-FITC和PI染色法检测凋亡细胞的百分率,用Western印迹检测药物干预下的K562细胞Caspase-3蛋白表达。结果:IC163以浓度依赖性方式有效地抑制K562细胞增殖,其抑制K562细胞增殖的IC50为18.1μmol/L;IC163以浓度依赖性方式诱导K562细胞凋亡并伴有Caspase-3蛋白表达上调和裂解激活。结论:IC163能够以浓度依赖性方式有效地抑制K562细胞增殖并诱导K562细胞凋亡,其诱导K562细胞的机制可能与Caspase-3凋亡信号启动有关。Objective:To determine the effects of growth inhibition and apoptosis induction of IC163 on K562 leukemia cells. Method:K562 cells were treated with different concentrations of IC163. The cell viability were analyzed with MTT assay, the percentage of apoptosis cells was analyzed by Hoehest33258 staining and Annexin V/ PI via flow cytometric. Result..IC163 can significantly inhibit the proliferation of K562 cells in a concentration--dependent manner, and the IC50 was 18.1 μmol/L; IC163 can induce the apoptosis of K562 cells with an up-regulated Caspase-3 expression and cleavage actation. Conclusion: IC163 could efficiently inhibit the proliferation of K562 cells and induce the apoptosis of K562 cells. So IC163 maybe a potencial anti-leukemia drug.
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