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作 者:司马军 陈健[2] 刘丹丹[2] 沈健[2] 王索安[2] 郑鸣之[2] 仇容[2]
机构地区:[1]浙江省杭州红十字会医院普外科,杭州310004 [2]浙江医学高等专科学校
出 处:《中国中西医结合外科杂志》2012年第1期39-42,共4页Chinese Journal of Surgery of Integrated Traditional and Western Medicine
基 金:浙江省中医药科技计划项目(2010ZB022);浙江省嘉兴市科技计划项目(2010AY1017);浙江省医药卫生科研基金项目(2008A033)
摘 要:目的:观察菊米提取液对人结肠癌细胞增殖和凋亡的影响。方法:用不同浓度的菊米提取液处理SW620细胞,MTT法检测菊米提取液对SW620细胞增殖的抑制作用;流式细胞术检测细胞凋亡率;比色法测定Caspase-3/7酶和Caspase-6酶活性。结果:菊米提取液对SW620细胞增殖有抑制作用,IC50为0.012mg/mL,且呈一定的量效关系;随着药物浓度的增加(0.001、0.002、0.005、0.01mg/mL),细胞凋亡率分别为(6.46±0.02)%、(9.77±0.01)%、(13.11±0.04)%、(18.47±0.05)%,对照组细胞凋亡发生率为(4.83±0.01)%,显示菊米提取液诱导的细胞凋亡作用随浓度的增大而增加。同时Caspase-3/7酶和Caspase-6酶活性显著增强。结论:菊米提取液在能抑制体外培养的SW620细胞增殖并诱导其凋亡,Caspase-3、6、7活性增强可能是菊米提取液诱导SW620细胞凋亡的机制之一。Objective To explore the effect of Jumi extract on proliferation and apoptosis of human colon cancer cell line SW620.Methods SW620 cells and culture media containing Jumi extract (0.001,0.002,0.005,or 0.01 mg/mL) were co-incubated for 48 h.Cell proliferation rate,cell apoptosis,caspase-3/7 and caspase-6 activity were determined by methyl thiazolyl tetrazolium (MTT) colorimetric assay,flow cytometry analysis and spectrophotometric detection,respectively.Results The proliferation of SW620 cells was significantly inhibited by Jumi extract (0.001-0.01 mg/mL) in a dose-dependent manner.IC50 is 0.012mg/mL.Apoptosis rates in the cells treated with Jumi extract (0.001,0.002,0.005,or 0.01 mg/mL) were (6.46±0.02)%,(9.77±0.01)%,(13.11±0.04)% and (18.47±0.05)% respectively,which were higher than those in the control group (4.83±0.01) %.Compared with the control group,caspase-3/7 and caspase-6 activity were significantly increased in all Jumi treated groups.Conclusion The Jumi extract can inhibit the proliferation of colon cancer cell line SW620 in vitro in a dose-dependent manner and promote cell apoptosis through caspase-3,caspase-7 and caspase-6 pathway.
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